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918f0221b9696d05b579ebbf46da469bbd562290
rdkit/Code/GraphMol/catch_graphmol.cpp
Ric 918f0221b9 Make atom, bond iterators usable in STL algorithms (#5204) 
* add fwditerator features

* add a test
2022-04-15 06:57:57 +02:00

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//
// Copyright (C) 2018-2021 Greg Landrum and other RDKit contributors
//
// @@ All Rights Reserved @@
// This file is part of the RDKit.
// The contents are covered by the terms of the BSD license
// which is included in the file license.txt, found at the root
// of the RDKit source tree.
//
#include "catch.hpp"
#include <algorithm>
#include <limits>
#include <boost/format.hpp>
#include <GraphMol/RDKitBase.h>
#include <GraphMol/new_canon.h>
#include <GraphMol/RDKitQueries.h>
#include <GraphMol/Chirality.h>
#include <GraphMol/MonomerInfo.h>
#include <GraphMol/FileParsers/FileParsers.h>
#include <GraphMol/FileParsers/SequenceParsers.h>
#include <GraphMol/SmilesParse/SmilesParse.h>
#include <GraphMol/SmilesParse/SmilesWrite.h>
#include <GraphMol/SmilesParse/SmartsWrite.h>
using namespace RDKit;
#if 1
TEST_CASE("SMILES Parsing works", "[molops]") {
std::unique_ptr<RWMol> mol(SmilesToMol("C1CC1"));
REQUIRE(mol);
REQUIRE(mol->getNumAtoms() == 3);
}
TEST_CASE("Sanitization tests", "[molops]") {
std::unique_ptr<RWMol> mol(SmilesToMol("C1=CC=CC=C1Cc2ccccc2", false, false));
REQUIRE(mol);
REQUIRE(mol->getNumAtoms() == 13);
SECTION("properties") {
mol->updatePropertyCache();
CHECK(mol->getAtomWithIdx(0)->getTotalNumHs() == 1);
CHECK(!mol->getAtomWithIdx(0)->getIsAromatic());
CHECK(mol->getAtomWithIdx(10)->getIsAromatic());
SECTION("aromaticity") {
unsigned int opThatFailed;
MolOps::sanitizeMol(*mol, opThatFailed, MolOps::SANITIZE_SETAROMATICITY);
// mol->debugMol(std::cerr);
CHECK(mol->getAtomWithIdx(10)->getIsAromatic());
// blocked by #1730
// CHECK(mol->getAtomWithIdx(0)->getIsAromatic());
}
SECTION("kekulize") {
unsigned int opThatFailed;
MolOps::sanitizeMol(*mol, opThatFailed, MolOps::SANITIZE_KEKULIZE);
CHECK(!mol->getAtomWithIdx(0)->getIsAromatic());
CHECK(!mol->getAtomWithIdx(10)->getIsAromatic());
}
}
}
TEST_CASE("Github #2062", "[bug][molops]") {
SmilesParserParams ps;
ps.removeHs = false;
ps.sanitize = true;
std::unique_ptr<RWMol> mol(SmilesToMol("[C:1][C:2]([H:3])([H])[O:4][H]", ps));
REQUIRE(mol);
CHECK(mol->getNumAtoms() == 6);
mol->getAtomWithIdx(1)->setProp("intProp", 42);
MolOps::mergeQueryHs(*mol);
CHECK(mol->getNumAtoms() == 3);
SECTION("basics") { CHECK(mol->getAtomWithIdx(1)->getAtomMapNum() == 2); }
SECTION("other props") {
REQUIRE(mol->getAtomWithIdx(1)->hasProp("intProp"));
CHECK(mol->getAtomWithIdx(1)->getProp<int>("intProp") == 42);
}
}
TEST_CASE("Github #2086", "[bug][molops]") {
SECTION("reported version") {
auto mol = "C1CCCC1"_smiles;
REQUIRE(mol);
MolOps::addHs(*mol);
REQUIRE(mol->getNumAtoms() == 15);
mol->removeBond(4, 13);
MolOps::removeHs(*mol);
REQUIRE(mol->getNumAtoms() == 6);
}
}
TEST_CASE("github #299", "[bug][molops][SSSR]") {
SECTION("simplified") {
auto mol =
"C13%13%14.C124%18.C25%13%15.C368%17.C4679.C75%10%17.C8%11%14%16.C9%11%12%18.C%10%12%15%16"_smiles;
REQUIRE(mol);
REQUIRE(mol->getNumAtoms() == 9);
}
SECTION("old example from molopstest") {
auto mol = "C123C45C11C44C55C22C33C14C523"_smiles;
REQUIRE(mol);
REQUIRE(mol->getNumAtoms() == 9);
}
SECTION("carborane") {
std::unique_ptr<RWMol> mol(
SmilesToMol("[B]1234[B]567[B]118[B]229[B]33%10[B]454[B]656[B]711[B]822["
"C]933[B]%1045[C]6123",
0, false));
REQUIRE(mol);
CHECK(mol->getNumAtoms() == 12);
mol->updatePropertyCache(false);
MolOps::findSSSR(*mol);
REQUIRE(mol->getRingInfo()->isInitialized());
}
SECTION("original report from ChEbI") {
std::string pathName = getenv("RDBASE");
pathName += "/Code/GraphMol/test_data/";
std::unique_ptr<RWMol> mol(
MolFileToMol(pathName + "ChEBI_50252.mol", false));
REQUIRE(mol);
CHECK(mol->getNumAtoms() == 80);
mol->updatePropertyCache(false);
MolOps::findSSSR(*mol);
REQUIRE(mol->getRingInfo()->isInitialized());
}
}
TEST_CASE("github #2224", "[bug][molops][removeHs][query]") {
SECTION("the original report") {
std::string pathName = getenv("RDBASE");
pathName += "/Code/GraphMol/test_data/";
std::unique_ptr<RWMol> mol(MolFileToMol(pathName + "github2224_1.mol"));
REQUIRE(mol);
REQUIRE(mol->getNumAtoms() == 7);
}
SECTION("basics") {
SmilesParserParams ps;
ps.removeHs = false;
ps.sanitize = true;
std::unique_ptr<ROMol> mol(SmilesToMol("C[H]", ps));
REQUIRE(mol);
REQUIRE(mol->getNumAtoms() == 2);
{ // The H without a query is removed
std::unique_ptr<ROMol> m2(MolOps::removeHs(*mol));
CHECK(m2->getNumAtoms() == 1);
}
{ // but if we add a query feature it's not removed
RWMol m2(*mol);
auto *qa = new QueryAtom(1);
m2.replaceAtom(1, qa);
m2.getAtomWithIdx(1)->setAtomicNum(1);
MolOps::removeHs(m2);
CHECK(m2.getNumAtoms() == 2);
delete qa;
}
}
}
TEST_CASE(
"github #2268: Recognize N in three-membered rings as potentially chiral",
"[bug][stereo]") {
SECTION("basics: N in a 3 ring") {
const auto mol = "C[N@]1CC1C"_smiles;
REQUIRE(mol);
CHECK(mol->getAtomWithIdx(1)->getChiralTag() != Atom::CHI_UNSPECIFIED);
}
SECTION("basics: N in a 4 ring") {
const auto mol = "C[N@]1CCC1C"_smiles;
REQUIRE(mol);
CHECK(mol->getAtomWithIdx(1)->getChiralTag() == Atom::CHI_UNSPECIFIED);
}
SECTION("the original molecule") {
std::string mb = R"CTAB(
Mrv1810 02131915062D
18 20 0 0 1 0 999 V2000
-0.7207 -1.3415 0.0000 N 0 0 1 0 0 0 0 0 0 0 0 0
-0.0583 -0.8416 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
-0.0083 -1.7540 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.3956 -0.8666 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0
-0.3250 -0.0667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.1955 -0.6499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.1499 -0.0792 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.6541 -0.4292 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.7830 -1.2291 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.6081 -1.6623 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.4080 0.1500 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1.3665 -0.8374 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.6416 0.3958 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.1996 0.3708 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.4121 1.1624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.3498 0.8207 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.0790 -0.4167 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.0665 0.4083 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2 1 1 0 0 0 0
1 3 1 1 0 0 0
4 1 1 0 0 0 0
5 2 1 0 0 0 0
4 6 1 0 0 0 0
7 4 1 0 0 0 0
2 8 1 6 0 0 0
9 6 2 0 0 0 0
4 10 1 1 0 0 0
11 6 1 0 0 0 0
12 8 2 0 0 0 0
13 8 1 0 0 0 0
14 11 1 0 0 0 0
15 14 1 0 0 0 0
16 13 2 0 0 0 0
17 12 1 0 0 0 0
18 16 1 0 0 0 0
2 3 1 0 0 0 0
5 7 1 0 0 0 0
17 18 2 0 0 0 0
M END
)CTAB";
std::unique_ptr<ROMol> mol(MolBlockToMol(mb));
REQUIRE(mol);
CHECK(mol->getAtomWithIdx(0)->getChiralTag() != Atom::CHI_UNSPECIFIED);
}
}
TEST_CASE("github #2244", "[bug][molops][stereo]") {
SECTION("the original report") {
auto mol = "CC=CC=CC"_smiles;
REQUIRE(mol);
MolOps::findPotentialStereoBonds(*mol, true);
CHECK(mol->getBondWithIdx(1)->getStereo() == Bond::STEREOANY);
CHECK(mol->getBondWithIdx(3)->getStereo() == Bond::STEREOANY);
mol->getBondWithIdx(3)->setStereo(Bond::STEREONONE);
MolOps::findPotentialStereoBonds(*mol, true);
CHECK(mol->getBondWithIdx(1)->getStereo() == Bond::STEREOANY);
CHECK(mol->getBondWithIdx(3)->getStereo() == Bond::STEREOANY);
}
}
TEST_CASE(
"github #2258: heterocycles with exocyclic bonds not failing valence check",
"[bug][molops]") {
SECTION("the original report") {
std::vector<std::string> smiles = {"C=n1ccnc1", "C#n1ccnc1"};
for (auto smi : smiles) {
CHECK_THROWS_AS(SmilesToMol(smi), MolSanitizeException);
}
}
}
TEST_CASE("github #908: AddHs() using 3D coordinates with 2D conformations",
"[bug][molops]") {
SECTION("basics: single atom mols") {
std::vector<std::string> smiles = {"Cl", "O", "N", "C"};
for (auto smi : smiles) {
// std::cerr << smi << std::endl;
std::unique_ptr<RWMol> mol(SmilesToMol(smi));
REQUIRE(mol);
auto conf = new Conformer(1);
conf->set3D(false);
conf->setAtomPos(0, RDGeom::Point3D(0, 0, 0));
mol->addConformer(conf, true);
bool explicitOnly = false;
bool addCoords = true;
MolOps::addHs(*mol, explicitOnly, addCoords);
for (size_t i = 0; i < mol->getNumAtoms(); ++i) {
// std::cerr << " " << i << " " << conf->getAtomPos(i) << std::endl;
CHECK(conf->getAtomPos(i).z == 0.0);
}
}
}
}
TEST_CASE(
"github #2437: Canon::rankMolAtoms results in crossed double bonds in "
"rings",
"[bug][molops]") {
SECTION("underlying problem") {
std::string molb = R"CTAB(testmol
Mrv1824 05081910082D
4 4 0 0 0 0 999 V2000
6.9312 -8.6277 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.9312 -9.4527 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.7562 -8.6277 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.7562 -9.4527 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0 0 0 0
1 3 1 0 0 0 0
3 4 1 0 0 0 0
2 4 2 0 0 0 0
M END
)CTAB";
bool sanitize = false;
bool removeHs = false;
std::unique_ptr<RWMol> mol(MolBlockToMol(molb, sanitize, removeHs));
REQUIRE(mol);
mol->updatePropertyCache();
CHECK(mol->getBondWithIdx(3)->getBondType() == Bond::BondType::DOUBLE);
CHECK(mol->getBondWithIdx(3)->getBondDir() == Bond::BondDir::NONE);
std::vector<unsigned int> ranks;
CHECK(!mol->getRingInfo()->isInitialized());
Canon::rankMolAtoms(*mol, ranks);
}
SECTION("as discovered") {
std::string molb = R"CTAB(testmol
Mrv1824 05081910082D
4 4 0 0 0 0 999 V2000
6.9312 -9.4527 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.7562 -8.6277 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.7562 -9.4527 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.9312 -8.6277 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0 0 0 0
1 3 1 0 0 0 0
3 4 1 0 0 0 0
2 4 2 0 0 0 0
M END
)CTAB";
bool sanitize = false;
bool removeHs = false;
std::unique_ptr<RWMol> mol(MolBlockToMol(molb, sanitize, removeHs));
REQUIRE(mol);
mol->updatePropertyCache();
CHECK(mol->getBondWithIdx(3)->getBondType() == Bond::BondType::DOUBLE);
CHECK(mol->getBondWithIdx(3)->getBondDir() == Bond::BondDir::NONE);
auto nmb = MolToMolBlock(*mol);
CHECK(nmb.find("2 4 2 3") == std::string::npos);
CHECK(nmb.find("2 4 2 0") != std::string::npos);
std::vector<unsigned int> ranks;
Canon::rankMolAtoms(*mol, ranks);
nmb = MolToMolBlock(*mol);
CHECK(nmb.find("2 4 2 3") == std::string::npos);
CHECK(nmb.find("2 4 2 0") != std::string::npos);
}
}
TEST_CASE(
"github #2423: Incorrect assignment of explicit Hs to Al+3 read from mol "
"block",
"[bug][molops]") {
SECTION("basics: single atom mols") {
std::string mb = R"CTAB(2300
-OEChem-01301907122D
1 0 0 0 0 0 0 0 0999 V2000
-66.7000 999.0000 0.0000 Al 0 1 0 0 0 0 0 0 0 0 0 0
M CHG 1 1 3
M END)CTAB";
std::unique_ptr<ROMol> mol(MolBlockToMol(mb));
REQUIRE(mol);
CHECK(mol->getAtomWithIdx(0)->getFormalCharge() == 3);
CHECK(mol->getAtomWithIdx(0)->getTotalNumHs() == 0);
}
}
TEST_CASE("Specialized exceptions for sanitization errors", "[molops]") {
SECTION("AtomValenceException") {
std::vector<std::pair<std::string, unsigned int>> smiles = {
{"C=n1ccnc1", 1}, {"CCO(C)C", 2}};
for (auto pr : smiles) {
CHECK_THROWS_AS(SmilesToMol(pr.first), AtomValenceException);
try {
auto m = SmilesToMol(pr.first);
RDUNUSED_PARAM(m);
} catch (const AtomValenceException &e) {
CHECK(e.getType() == "AtomValenceException");
CHECK(e.getAtomIdx() == pr.second);
}
}
}
SECTION("AtomKekulizeException") {
std::vector<std::pair<std::string, unsigned int>> smiles = {
{"CCcc", 2},
};
for (auto pr : smiles) {
CHECK_THROWS_AS(SmilesToMol(pr.first), AtomKekulizeException);
try {
auto m = SmilesToMol(pr.first);
RDUNUSED_PARAM(m);
} catch (const AtomKekulizeException &e) {
CHECK(e.getType() == "AtomKekulizeException");
CHECK(e.getAtomIdx() == pr.second);
}
}
}
SECTION("KekulizeException") {
std::vector<std::pair<std::string, std::vector<unsigned int>>> smiles = {
{"c1cccc1", {0, 1, 2, 3, 4}},
{"Cc1cc1", {1, 2, 3}},
{"C1:c:CC1", {0, 1, 2}}};
for (auto pr : smiles) {
CHECK_THROWS_AS(SmilesToMol(pr.first), KekulizeException);
try {
auto m = SmilesToMol(pr.first);
RDUNUSED_PARAM(m);
} catch (const KekulizeException &e) {
CHECK(e.getType() == "KekulizeException");
CHECK(e.getAtomIndices() == pr.second);
}
}
}
}
TEST_CASE("detectChemistryProblems", "[molops]") {
SECTION("Basics") {
SmilesParserParams ps;
ps.sanitize = false;
auto m = std::unique_ptr<ROMol>(SmilesToMol("CO(C)CFCc1cc1", ps));
REQUIRE(m);
auto res = MolOps::detectChemistryProblems(*m);
REQUIRE(res.size() == 3);
CHECK(res[0]->getType() == "AtomValenceException");
REQUIRE(dynamic_cast<AtomValenceException *>(res[0].get()));
CHECK(dynamic_cast<AtomSanitizeException *>(res[0].get())->getAtomIdx() ==
1);
CHECK(res[1]->getType() == "AtomValenceException");
REQUIRE(dynamic_cast<AtomSanitizeException *>(res[1].get()));
CHECK(dynamic_cast<AtomSanitizeException *>(res[1].get())->getAtomIdx() ==
4);
CHECK(res[2]->getType() == "KekulizeException");
REQUIRE(dynamic_cast<KekulizeException *>(res[2].get()));
CHECK(dynamic_cast<KekulizeException *>(res[2].get())->getAtomIndices() ==
std::vector<unsigned int>({6, 7, 8}));
}
SECTION("No problems") {
SmilesParserParams ps;
ps.sanitize = false;
auto m = std::unique_ptr<ROMol>(SmilesToMol("c1ccccc1", ps));
REQUIRE(m);
auto res = MolOps::detectChemistryProblems(*m);
REQUIRE(res.size() == 0);
}
}
TEST_CASE(
"github #2606: Bad valence corrections on Pb, Sn"
"[bug][molops]") {
SECTION("basics-Pb") {
std::string mb = R"CTAB(
Mrv1810 08141905562D
5 0 0 0 0 0 999 V2000
-3.6316 -0.4737 0.0000 Pb 0 0 0 0 0 0 0 0 0 0 0 0
-3.6541 0.3609 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
-2.4586 -0.5188 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
-3.6992 -1.5338 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
-4.5789 -0.4286 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
M CHG 5 1 4 2 -1 3 -1 4 -1 5 -1
M END
)CTAB";
std::unique_ptr<ROMol> mol(MolBlockToMol(mb));
REQUIRE(mol);
CHECK(mol->getAtomWithIdx(0)->getFormalCharge() == 4);
CHECK(mol->getAtomWithIdx(0)->getTotalNumHs() == 0);
}
SECTION("basics-Sn") {
std::string mb = R"CTAB(
Mrv1810 08141905562D
5 0 0 0 0 0 999 V2000
-3.6316 -0.4737 0.0000 Sn 0 0 0 0 0 0 0 0 0 0 0 0
-3.6541 0.3609 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
-2.4586 -0.5188 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
-3.6992 -1.5338 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
-4.5789 -0.4286 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
M CHG 5 1 4 2 -1 3 -1 4 -1 5 -1
M END
)CTAB";
std::unique_ptr<ROMol> mol(MolBlockToMol(mb));
REQUIRE(mol);
CHECK(mol->getAtomWithIdx(0)->getFormalCharge() == 4);
CHECK(mol->getAtomWithIdx(0)->getTotalNumHs() == 0);
}
SECTION("basics-Ge") {
std::string mb = R"CTAB(
Mrv1810 08141905562D
5 0 0 0 0 0 999 V2000
-3.6316 -0.4737 0.0000 Ge 0 0 0 0 0 0 0 0 0 0 0 0
-3.6541 0.3609 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
-2.4586 -0.5188 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
-3.6992 -1.5338 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
-4.5789 -0.4286 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
M CHG 5 1 4 2 -1 3 -1 4 -1 5 -1
M END
)CTAB";
std::unique_ptr<ROMol> mol(MolBlockToMol(mb));
REQUIRE(mol);
CHECK(mol->getAtomWithIdx(0)->getFormalCharge() == 4);
CHECK(mol->getAtomWithIdx(0)->getTotalNumHs() == 0);
}
}
TEST_CASE(
"github #2607: Pb, Sn should support valence 2"
"[bug][molops]") {
SECTION("basics-Pb") {
std::string mb = R"CTAB(
Mrv1810 08141905562D
3 0 0 0 0 0 999 V2000
-3.6316 -0.4737 0.0000 Pb 0 0 0 0 0 0 0 0 0 0 0 0
-3.6541 0.3609 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
-2.4586 -0.5188 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
M CHG 3 1 2 2 -1 3 -1
M END
)CTAB";
std::unique_ptr<ROMol> mol(MolBlockToMol(mb));
REQUIRE(mol);
CHECK(mol->getAtomWithIdx(0)->getFormalCharge() == 2);
CHECK(mol->getAtomWithIdx(0)->getTotalNumHs() == 0);
}
SECTION("basics-Sn") {
std::string mb = R"CTAB(
Mrv1810 08141905562D
3 0 0 0 0 0 999 V2000
-3.6316 -0.4737 0.0000 Sn 0 0 0 0 0 0 0 0 0 0 0 0
-3.6541 0.3609 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
-2.4586 -0.5188 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
M CHG 3 1 2 2 -1 3 -1
M END
)CTAB";
std::unique_ptr<ROMol> mol(MolBlockToMol(mb));
REQUIRE(mol);
CHECK(mol->getAtomWithIdx(0)->getFormalCharge() == 2);
CHECK(mol->getAtomWithIdx(0)->getTotalNumHs() == 0);
}
}
TEST_CASE(
"github #2649: Allenes read from mol blocks have crossed bonds assigned"
"[bug][stereochemistry]") {
SECTION("basics") {
std::string mb = R"CTAB(mol
Mrv1824 09191901002D
6 5 0 0 0 0 999 V2000
-1.6986 -7.4294 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.2522 -6.8245 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.1438 -8.0357 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.8095 -6.2156 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.3374 -7.8470 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.6162 -6.3886 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1 3 2 0 0 0 0
2 1 2 0 0 0 0
3 5 1 0 0 0 0
4 2 2 0 0 0 0
6 4 1 0 0 0 0
M END)CTAB";
std::unique_ptr<ROMol> mol(MolBlockToMol(mb));
REQUIRE(mol);
CHECK(mol->getBondWithIdx(0)->getStereo() == Bond::STEREONONE);
CHECK(mol->getBondWithIdx(1)->getStereo() == Bond::STEREONONE);
CHECK(mol->getBondWithIdx(3)->getStereo() == Bond::STEREONONE);
auto outmolb = MolToMolBlock(*mol);
// std::cerr<<outmolb<<std::endl;
CHECK(outmolb.find("1 3 2 0") != std::string::npos);
CHECK(outmolb.find("2 1 2 0") != std::string::npos);
CHECK(outmolb.find("4 2 2 0") != std::string::npos);
}
}
TEST_CASE(
"GitHub 2712: setBondStereoFromDirections() returning incorrect results"
"[stereochemistry]") {
SECTION("basics 1a") {
std::string mb = R"CTAB(
Mrv1810 10141909562D
4 3 0 0 0 0 999 V2000
3.3412 -2.9968 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5162 -2.9968 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1037 -3.7112 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.7537 -2.2823 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1 2 2 0 0 0 0
2 3 1 0 0 0 0
1 4 1 0 0 0 0
M END
)CTAB";
bool sanitize = false;
std::unique_ptr<ROMol> mol(MolBlockToMol(mb, sanitize));
REQUIRE(mol);
CHECK(mol->getBondWithIdx(0)->getBondType() == Bond::DOUBLE);
CHECK(mol->getBondWithIdx(0)->getStereo() == Bond::STEREONONE);
MolOps::setBondStereoFromDirections(*mol);
CHECK(mol->getBondWithIdx(0)->getStereo() == Bond::STEREOTRANS);
}
SECTION("basics 1b") {
std::string mb = R"CTAB(
Mrv1810 10141909562D
4 3 0 0 0 0 999 V2000
3.3412 -2.9968 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5162 -2.9968 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1037 -3.7112 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.7537 -2.2823 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1 2 2 0 0 0 0
2 3 1 0 0 0 0
4 1 1 0 0 0 0
M END
)CTAB";
bool sanitize = false;
std::unique_ptr<ROMol> mol(MolBlockToMol(mb, sanitize));
REQUIRE(mol);
CHECK(mol->getBondWithIdx(0)->getBondType() == Bond::DOUBLE);
CHECK(mol->getBondWithIdx(0)->getStereo() == Bond::STEREONONE);
MolOps::setBondStereoFromDirections(*mol);
CHECK(mol->getBondWithIdx(0)->getStereo() == Bond::STEREOTRANS);
}
SECTION("basics 2a") {
std::string mb = R"CTAB(
Mrv1810 10141909582D
4 3 0 0 0 0 999 V2000
3.4745 -5.2424 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6495 -5.2424 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2370 -5.9569 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.8870 -5.9569 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1 2 2 0 0 0 0
2 3 1 0 0 0 0
1 4 1 0 0 0 0
M END
)CTAB";
bool sanitize = false;
std::unique_ptr<ROMol> mol(MolBlockToMol(mb, sanitize));
REQUIRE(mol);
CHECK(mol->getBondWithIdx(0)->getBondType() == Bond::DOUBLE);
CHECK(mol->getBondWithIdx(0)->getStereo() == Bond::STEREONONE);
MolOps::setBondStereoFromDirections(*mol);
CHECK(mol->getBondWithIdx(0)->getStereo() == Bond::STEREOCIS);
}
SECTION("basics 2b") {
std::string mb = R"CTAB(
Mrv1810 10141909582D
4 3 0 0 0 0 999 V2000
3.4745 -5.2424 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6495 -5.2424 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2370 -5.9569 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.8870 -5.9569 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1 2 2 0 0 0 0
2 3 1 0 0 0 0
4 1 1 0 0 0 0
M END
)CTAB";
bool sanitize = false;
std::unique_ptr<ROMol> mol(MolBlockToMol(mb, sanitize));
REQUIRE(mol);
CHECK(mol->getBondWithIdx(0)->getBondType() == Bond::DOUBLE);
CHECK(mol->getBondWithIdx(0)->getStereo() == Bond::STEREONONE);
MolOps::setBondStereoFromDirections(*mol);
CHECK(mol->getBondWithIdx(0)->getStereo() == Bond::STEREOCIS);
}
}
TEST_CASE("removeHs screwing up double bond stereo", "[bug][removeHs]") {
SECTION("example1") {
std::string molblock = R"CTAB(molblock = """
SciTegic12221702182D
47 51 0 0 0 0 999 V2000
0.2962 6.2611 0.0000 C 0 0
-3.9004 4.4820 0.0000 C 0 0
1.4195 5.2670 0.0000 C 0 0
-3.8201 -7.4431 0.0000 C 0 0
-4.9433 -6.4490 0.0000 C 0 0
-2.3975 -6.9674 0.0000 C 0 0
3.5921 -3.5947 0.0000 C 0 0
-3.1475 2.3700 0.0000 C 0 0
2.1695 -4.0705 0.0000 C 0 0
-2.0242 1.3759 0.0000 C 0 0
-4.6440 -4.9792 0.0000 C 0 0
2.7681 -1.1308 0.0000 C 0 0
-5.8626 1.1332 0.0000 C 0 0
3.0674 0.3391 0.0000 C 0 0
3.6660 3.2787 0.0000 C 0 0
8.1591 -0.6978 0.0000 C 0 0
7.3351 1.7662 0.0000 C 0 0
-6.3876 3.5028 0.0000 C 0 0
-0.6756 -5.0219 0.0000 C 0 0
7.0358 0.2964 0.0000 C 0 0
3.8914 -2.1249 0.0000 C 0 0
-2.0982 -5.4976 0.0000 C 0 0
-4.5701 1.8943 0.0000 C 0 0 1 0 0 0
-6.9859 2.1273 0.0000 C 0 0 1 0 0 0
4.4900 0.8148 0.0000 C 0 0
1.3455 -1.6065 0.0000 C 0 0
4.7893 2.2846 0.0000 C 0 0
1.9442 1.3332 0.0000 C 0 0
1.0462 -3.0763 0.0000 C 0 0
2.2435 2.8030 0.0000 C 0 0
-0.6017 1.8516 0.0000 C 0 0
5.6132 -0.1794 0.0000 C 0 0
0.2223 -0.6124 0.0000 Cl 0 0
9.2823 -1.6919 0.0000 N 0 0
-3.2215 -4.5035 0.0000 N 0 0
6.2119 2.7603 0.0000 N 0 0
5.3139 -1.6492 0.0000 N 0 0
0.5216 0.8575 0.0000 N 0 0
-4.8945 3.3588 0.0000 N 0 0
-8.2913 2.8662 0.0000 O 0 0
-0.3024 3.3214 0.0000 O 0 0
1.1202 3.7971 0.0000 O 0 0
-0.3763 -3.5520 0.0000 O 0 0
-2.8482 3.8398 0.0000 H 0 0
-2.3235 -0.0940 0.0000 H 0 0
-3.9483 0.5292 0.0000 H 0 0
-7.8572 0.9063 0.0000 H 0 0
1 3 1 0
2 39 1 0
3 42 1 0
4 5 2 0
4 6 1 0
5 11 1 0
6 22 2 0
7 9 2 0
7 21 1 0
8 44 1 0
8 10 2 0
8 23 1 0
9 29 1 0
10 45 1 0
10 31 1 0
11 35 2 0
12 21 2 0
12 26 1 0
13 23 1 0
13 24 1 0
14 25 2 0
14 28 1 0
15 27 2 0
15 30 1 0
16 20 1 0
16 34 3 0
17 20 2 0
17 36 1 0
18 24 1 0
18 39 1 0
19 22 1 0
19 43 1 0
20 32 1 0
21 37 1 0
22 35 1 0
23 46 1 6
23 39 1 0
24 47 1 1
24 40 1 0
25 27 1 0
25 32 1 0
26 29 2 0
26 33 1 0
27 36 1 0
28 30 2 0
28 38 1 0
29 43 1 0
30 42 1 0
31 38 2 0
31 41 1 0
32 37 2 3
M END
"""
)CTAB";
bool sanitize = false;
bool removeHs = false;
std::unique_ptr<RWMol> m(MolBlockToMol(molblock, sanitize, removeHs));
REQUIRE(m);
m->updatePropertyCache();
MolOps::setBondStereoFromDirections(*m);
CHECK(m->getBondWithIdx(10)->getBondType() == Bond::DOUBLE);
CHECK(m->getBondWithIdx(10)->getStereo() == Bond::STEREOTRANS);
REQUIRE(m->getBondWithIdx(10)->getStereoAtoms().size() == 2);
CHECK(m->getBondWithIdx(10)->getStereoAtoms()[0] == 43);
CHECK(m->getBondWithIdx(10)->getStereoAtoms()[1] == 44);
MolOps::removeHs(*m); // implicitOnly,updateExplicitCount,sanitize);
// m->debugMol(std::cerr);
CHECK(m->getBondWithIdx(9)->getBondType() == Bond::DOUBLE);
CHECK(m->getBondWithIdx(9)->getStereo() == Bond::STEREOTRANS);
REQUIRE(m->getBondWithIdx(9)->getStereoAtoms().size() == 2);
CHECK(m->getBondWithIdx(9)->getStereoAtoms()[0] == 22);
CHECK(m->getBondWithIdx(9)->getStereoAtoms()[1] == 30);
}
}
TEST_CASE("setDoubleBondNeighborDirections()", "[stereochemistry][bug]") {
SECTION("basics cis") {
auto m = "CC=CC"_smiles;
REQUIRE(m);
m->getBondWithIdx(1)->getStereoAtoms() = {0, 3};
m->getBondWithIdx(1)->setStereo(Bond::STEREOCIS);
MolOps::setDoubleBondNeighborDirections(*m);
CHECK(m->getBondWithIdx(0)->getBondDir() == Bond::ENDUPRIGHT);
CHECK(m->getBondWithIdx(2)->getBondDir() == Bond::ENDDOWNRIGHT);
CHECK(MolToSmiles(*m) == "C/C=C\\C");
}
SECTION("basics trans") {
auto m = "CC=CC"_smiles;
REQUIRE(m);
m->getBondWithIdx(1)->getStereoAtoms() = {0, 3};
m->getBondWithIdx(1)->setStereo(Bond::STEREOTRANS);
MolOps::setDoubleBondNeighborDirections(*m);
CHECK(m->getBondWithIdx(0)->getBondDir() == Bond::ENDUPRIGHT);
CHECK(m->getBondWithIdx(2)->getBondDir() == Bond::ENDUPRIGHT);
CHECK(MolToSmiles(*m) == "C/C=C/C");
}
SECTION("swap (Github #3322)") {
auto m = "CC=CC"_smiles;
REQUIRE(m);
m->getBondWithIdx(1)->getStereoAtoms() = {0, 3};
m->getBondWithIdx(1)->setStereo(Bond::STEREOTRANS);
MolOps::setDoubleBondNeighborDirections(*m);
CHECK(m->getBondWithIdx(0)->getBondDir() == Bond::ENDUPRIGHT);
CHECK(m->getBondWithIdx(2)->getBondDir() == Bond::ENDUPRIGHT);
CHECK(MolToSmiles(*m) == "C/C=C/C");
m->clearComputedProps();
m->getBondWithIdx(1)->getStereoAtoms() = {0, 3};
m->getBondWithIdx(1)->setStereo(Bond::STEREOCIS);
MolOps::setDoubleBondNeighborDirections(*m);
CHECK(m->getBondWithIdx(0)->getBondDir() == Bond::ENDUPRIGHT);
CHECK(m->getBondWithIdx(2)->getBondDir() == Bond::ENDDOWNRIGHT);
CHECK(MolToSmiles(*m) == "C/C=C\\C");
}
}
TEST_CASE("github #2782: addHs() fails on atoms with 'bad' valences", "[bug]") {
SECTION("basics") {
SmilesParserParams ps;
ps.sanitize = false;
std::unique_ptr<RWMol> m(
static_cast<RWMol *>(SmilesToMol("C=C1=CC=CC=C1", ps)));
REQUIRE(m);
bool strict = false;
m->updatePropertyCache(strict);
CHECK(m->getNumAtoms() == 7);
MolOps::addHs(*m);
CHECK(m->getNumAtoms() == 14);
// this doesn't change the fact that there's still a bad valence present:
CHECK_THROWS_AS(m->updatePropertyCache(), AtomValenceException);
}
}
TEST_CASE(
"Github #2784: Element symbol lookup for some transuranics returns "
"incorrect results",
"[transuranics][bug]") {
auto pt = PeriodicTable::getTable();
SECTION("number to symbol") {
std::vector<std::pair<unsigned int, std::string>> data = {
{113, "Nh"}, {114, "Fl"}, {115, "Mc"},
{116, "Lv"}, {117, "Ts"}, {118, "Og"}};
for (const auto &pr : data) {
CHECK(pt->getElementSymbol(pr.first) == pr.second);
}
}
SECTION("symbol to number") {
std::vector<std::pair<int, std::string>> data = {
{113, "Nh"}, {114, "Fl"}, {115, "Mc"}, {116, "Lv"},
{117, "Ts"}, {118, "Og"}, {113, "Uut"}, {115, "Uup"}};
for (const auto &pr : data) {
CHECK(pt->getAtomicNumber(pr.second) == pr.first);
}
}
}
TEST_CASE("github #2775", "[valence][bug]") {
SECTION("basics") {
std::string molblock = R"CTAB(bismuth citrate
Mrv1810 11111908592D
14 12 0 0 0 0 999 V2000
7.4050 -0.5957 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.6906 -1.0082 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.9761 -0.5957 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.6906 -1.8332 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
7.4050 0.2293 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.5800 0.2293 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.1675 0.9438 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.5800 1.6583 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.3425 0.9438 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
8.2300 0.2293 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.6425 -0.4851 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.6425 0.9438 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0
7.4050 1.0543 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.5175 0.9438 0.0000 Bi 0 1 0 0 0 0 0 0 0 0 0 0
1 2 1 0 0 0 0
2 3 2 0 0 0 0
2 4 1 0 0 0 0
1 5 1 0 0 0 0
5 6 1 0 0 0 0
6 7 1 0 0 0 0
7 8 2 0 0 0 0
7 9 1 0 0 0 0
5 10 1 0 0 0 0
10 11 2 0 0 0 0
10 12 1 0 0 0 0
5 13 1 0 0 0 0
M CHG 4 4 -1 9 -1 12 -1 14 3
M END
)CTAB";
std::unique_ptr<RWMol> m(MolBlockToMol(molblock));
REQUIRE(m);
CHECK(m->getAtomWithIdx(13)->getSymbol() == "Bi");
CHECK(m->getAtomWithIdx(13)->getNumImplicitHs() == 0);
}
}
TEST_CASE("RemoveHsParameters", "[molops]") {
SmilesParserParams smilesPs;
smilesPs.removeHs = false;
SECTION("H-H") {
std::unique_ptr<RWMol> m{SmilesToMol("[H][H].[H]O[H]", smilesPs)};
REQUIRE(m);
CHECK(m->getNumAtoms() == 5);
{
RWMol cp(*m);
MolOps::removeHs(cp);
CHECK(cp.getNumAtoms() == 3);
}
{
MolOps::RemoveHsParameters ps;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 3);
}
{
MolOps::RemoveHsParameters ps;
ps.removeOnlyHNeighbors = true;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 1);
}
}
SECTION("dummies") {
std::unique_ptr<RWMol> m{SmilesToMol("[H][*]O[H]", smilesPs)};
REQUIRE(m);
CHECK(m->getNumAtoms() == 4);
{
RWMol cp(*m);
MolOps::removeHs(cp);
CHECK(cp.getNumAtoms() == 3);
}
{
MolOps::RemoveHsParameters ps;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 3);
}
{
MolOps::RemoveHsParameters ps;
ps.removeDummyNeighbors = true;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 2);
}
}
SECTION("chiralHs") {
std::unique_ptr<RWMol> m{SmilesToMol("[C@]12([H])CCC1CO2", smilesPs)};
REQUIRE(m);
CHECK(m->getNumAtoms() == 7);
// artificial wedging since we don't have a conformer
m->getBondBetweenAtoms(0, 1)->setBondDir(Bond::BEGINWEDGE);
{
RWMol cp(*m);
MolOps::removeHs(cp);
CHECK(cp.getNumAtoms() == 6);
}
{
MolOps::RemoveHsParameters ps;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 6);
}
{
MolOps::RemoveHsParameters ps;
ps.removeWithWedgedBond = false;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 7);
}
}
SECTION("degree zero") {
std::unique_ptr<RWMol> m{SmilesToMol("[F-].[H+]", smilesPs)};
REQUIRE(m);
CHECK(m->getNumAtoms() == 2);
{
RWMol cp(*m);
MolOps::removeHs(cp);
CHECK(cp.getNumAtoms() == 2);
}
{
MolOps::RemoveHsParameters ps;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 2);
}
{
MolOps::RemoveHsParameters ps;
ps.removeDegreeZero = true;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 1);
}
}
SECTION("isotopes") {
std::unique_ptr<RWMol> m{SmilesToMol("F[2H]", smilesPs)};
REQUIRE(m);
CHECK(m->getNumAtoms() == 2);
{
RWMol cp(*m);
MolOps::removeHs(cp);
CHECK(cp.getNumAtoms() == 2);
}
{
MolOps::RemoveHsParameters ps;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 2);
}
{
MolOps::RemoveHsParameters ps;
ps.removeIsotopes = true;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 1);
}
}
SECTION("defining bond stereo") {
std::unique_ptr<RWMol> m{SmilesToMol("F/C=N/[H]", smilesPs)};
REQUIRE(m);
CHECK(m->getNumAtoms() == 4);
{
RWMol cp(*m);
MolOps::removeHs(cp);
CHECK(cp.getNumAtoms() == 4);
}
{
MolOps::RemoveHsParameters ps;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 4);
}
{
MolOps::RemoveHsParameters ps;
ps.removeDefiningBondStereo = true;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 3);
}
}
SECTION("Query atoms") {
std::unique_ptr<RWMol> m{SmartsToMol("O[#1]")};
REQUIRE(m);
CHECK(m->getNumAtoms() == 2);
{
RWMol cp(*m);
MolOps::removeHs(cp);
CHECK(cp.getNumAtoms() == 2);
}
{
MolOps::RemoveHsParameters ps;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 2);
}
{
MolOps::RemoveHsParameters ps;
ps.removeWithQuery = true;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 1);
}
}
SECTION("higher degree") {
// this is a silly example
std::unique_ptr<RWMol> m{SmilesToMol("F[H-]F", smilesPs)};
REQUIRE(m);
CHECK(m->getNumAtoms() == 3);
{
RWMol cp(*m);
MolOps::removeHs(cp);
CHECK(cp.getNumAtoms() == 3);
}
{
MolOps::RemoveHsParameters ps;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 3);
}
{
MolOps::RemoveHsParameters ps;
ps.removeHigherDegrees = true;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 2);
}
}
SECTION("mapped Hs") {
std::unique_ptr<RWMol> m{SmilesToMol("[H:1]O[H]", smilesPs)};
REQUIRE(m);
CHECK(m->getNumAtoms() == 3);
{
RWMol cp(*m);
MolOps::removeHs(cp);
CHECK(cp.getNumAtoms() == 1);
}
{
MolOps::RemoveHsParameters ps;
ps.removeMapped = false;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 2);
}
}
SECTION("allHs") {
std::unique_ptr<RWMol> m{SmilesToMol(
"[C@]12([H])CCC1CO2.[H+].F[H-]F.[H][H].[H]*.F/C=C/[H]", smilesPs)};
REQUIRE(m);
// artificial wedging since we don't have a conformer
m->getBondBetweenAtoms(0, 1)->setBondDir(Bond::BEGINWEDGE);
RWMol cp(*m);
MolOps::removeAllHs(cp);
for (auto atom : cp.atoms()) {
CHECK(atom->getAtomicNum() != 1);
}
}
SECTION("allHs2") {
std::unique_ptr<ROMol> m{SmilesToMol(
"[C@]12([H])CCC1CO2.[H+].F[H-]F.[H][H].[H]*.F/C=C/[H]", smilesPs)};
REQUIRE(m);
// artificial wedging since we don't have a conformer
m->getBondBetweenAtoms(0, 1)->setBondDir(Bond::BEGINWEDGE);
std::unique_ptr<ROMol> cp{MolOps::removeAllHs(*m)};
for (auto atom : cp->atoms()) {
CHECK(atom->getAtomicNum() != 1);
}
}
}
#endif
TEST_CASE("github #2895: acepentalene aromaticity perception ",
"[molops][bug][aromaticity]") {
SECTION("acepentalene") {
std::unique_ptr<RWMol> m{SmilesToMol("C1=CC2=CC=C3C2=C1C=C3")};
REQUIRE(m);
auto smi = MolToSmiles(*m);
CHECK(smi == "C1=CC2=C3C1=CC=C3C=C2");
}
}
TEST_CASE("github #3256: fused ring aromaticity perception",
"[molops][bug][aromaticity]") {
SECTION("nitrogen only central ring") {
auto mol = "C1=CN2C3=CC=CN3C3=CC=CN3C2=C1"_smiles;
REQUIRE(mol);
for (const auto b : mol->bonds()) {
CHECK(b->getBondType() == Bond::AROMATIC);
}
auto smi = MolToSmiles(*mol);
CHECK(smi == "c1cc2n(c1)c1cccn1c1cccn21");
}
}
TEST_CASE("phosphine and arsine chirality", "[Chirality]") {
SECTION("chiral center recognized") {
auto mol1 = "C[P@](C1CCCC1)C1=CC=CC=C1"_smiles;
auto mol2 = "C[As@](C1CCCC1)C1=CC=CC=C1"_smiles;
REQUIRE(mol1);
REQUIRE(mol2);
CHECK(mol1->getAtomWithIdx(1)->getChiralTag() != Atom::CHI_UNSPECIFIED);
CHECK(mol2->getAtomWithIdx(1)->getChiralTag() != Atom::CHI_UNSPECIFIED);
}
SECTION("chiral center selective") {
auto mol1 = "C[P@](C)C1CCCCC1"_smiles;
auto mol2 = "C[As@](C)C1CCCCC1"_smiles;
REQUIRE(mol1);
REQUIRE(mol2);
CHECK(mol1->getAtomWithIdx(1)->getChiralTag() == Atom::CHI_UNSPECIFIED);
CHECK(mol2->getAtomWithIdx(1)->getChiralTag() == Atom::CHI_UNSPECIFIED);
}
SECTION("chiral center specific: P") {
auto mol1 = "C[P@](C1CCCC1)C1=CC=CC=C1"_smiles;
auto mol2 = "C[P@@](C1CCCC1)C1=CC=CC=C1"_smiles;
REQUIRE(mol1);
REQUIRE(mol2);
CHECK(MolToSmiles(*mol1) != MolToSmiles(*mol2));
}
SECTION("chiral center specific: As") {
auto mol1 = "C[As@](C1CCCC1)C1=CC=CC=C1"_smiles;
auto mol2 = "C[As@@](C1CCCC1)C1=CC=CC=C1"_smiles;
REQUIRE(mol1);
REQUIRE(mol2);
CHECK(MolToSmiles(*mol1) != MolToSmiles(*mol2));
}
SECTION("chiral center, implicit H: P") {
auto mol1 = "C[P@H]C1CCCCC1"_smiles;
auto mol2 = "C[P@@H]C1CCCCC1"_smiles;
REQUIRE(mol1);
REQUIRE(mol2);
CHECK(mol1->getAtomWithIdx(1)->getChiralTag() != Atom::CHI_UNSPECIFIED);
CHECK(mol1->getAtomWithIdx(1)->getChiralTag() != Atom::CHI_UNSPECIFIED);
}
SECTION("chiral center, implicit H: As") {
auto mol1 = "C[As@H]C1CCCCC1"_smiles;
auto mol2 = "C[As@@H]C1CCCCC1"_smiles;
REQUIRE(mol1);
REQUIRE(mol2);
CHECK(mol1->getAtomWithIdx(1)->getChiralTag() != Atom::CHI_UNSPECIFIED);
CHECK(mol1->getAtomWithIdx(1)->getChiralTag() != Atom::CHI_UNSPECIFIED);
}
SECTION("chiral center specific, implicit H: P") {
auto mol1 = "C[P@H]C1CCCCC1"_smiles;
auto mol2 = "C[P@@H]C1CCCCC1"_smiles;
REQUIRE(mol1);
REQUIRE(mol2);
CHECK(MolToSmiles(*mol1) != MolToSmiles(*mol2));
}
SECTION("chiral center specific, implicit H: As") {
auto mol1 = "C[As@H]C1CCCCC1"_smiles;
auto mol2 = "C[As@@H]C1CCCCC1"_smiles;
REQUIRE(mol1);
REQUIRE(mol2);
CHECK(MolToSmiles(*mol1) != MolToSmiles(*mol2));
}
}
TEST_CASE("github #2890", "[bug][molops][stereo]") {
auto mol = "CC=CC"_smiles;
REQUIRE(mol);
auto bond = mol->getBondWithIdx(1);
bond->setStereo(Bond::STEREOANY);
REQUIRE(bond->getStereoAtoms().empty());
MolOps::findPotentialStereoBonds(*mol);
CHECK(bond->getStereo() == Bond::STEREOANY);
CHECK(bond->getStereoAtoms().size() == 2);
}
TEST_CASE("github #3150 MolOps::removeHs removes hydrides", "[bug][molops]") {
SmilesParserParams smilesPs;
smilesPs.removeHs = false;
SECTION("Hydride ion remove Hydrides false") {
std::unique_ptr<RWMol> m{SmilesToMol("[H-]", smilesPs)};
REQUIRE(m);
MolOps::RemoveHsParameters ps;
ps.removeHydrides = false;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
// H atom not removed in this case because by default H atoms with degree 0
// are not removed
CHECK(cp.getNumAtoms() == 1);
CHECK(MolOps::getFormalCharge(cp) == -1);
}
SECTION("Hydride ion remove Hydrides true") {
std::unique_ptr<RWMol> m{SmilesToMol("[H-]", smilesPs)};
REQUIRE(m);
MolOps::RemoveHsParameters ps;
ps.removeHydrides = true;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
// H atom not removed in this case because by default H atoms with degree 0
// are not removed
CHECK(cp.getNumAtoms() == 1);
CHECK(MolOps::getFormalCharge(cp) == -1);
}
SECTION("Water") {
std::unique_ptr<RWMol> m{SmilesToMol("[OH+][H-]", smilesPs)};
REQUIRE(m);
MolOps::RemoveHsParameters ps;
ps.removeHydrides = false;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 2);
CHECK(MolOps::getFormalCharge(cp) == 0);
}
SECTION("Water remove Hydrides true") {
std::unique_ptr<RWMol> m{SmilesToMol("[OH+][H-]", smilesPs)};
REQUIRE(m);
MolOps::RemoveHsParameters ps;
ps.removeHydrides = true;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 1);
CHECK(MolOps::getFormalCharge(cp) == 1);
}
SECTION("Iron Hydride") {
std::unique_ptr<RWMol> m{SmilesToMol("[Fe+2]<-[H-]", smilesPs)};
REQUIRE(m);
MolOps::RemoveHsParameters ps;
ps.removeHydrides = false;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 2);
CHECK(MolOps::getFormalCharge(cp) == 1);
}
SECTION("Iron Hydride remove Hydrides") {
std::unique_ptr<RWMol> m{SmilesToMol("[Fe+2]<-[H-]", smilesPs)};
REQUIRE(m);
MolOps::RemoveHsParameters ps;
ps.removeHydrides = true;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 1);
CHECK(MolOps::getFormalCharge(cp) == 2);
}
SECTION("Ferrous Hydroxide") {
std::unique_ptr<RWMol> m{SmilesToMol("[Fe+2]<-[OH-]", smilesPs)};
REQUIRE(m);
MolOps::RemoveHsParameters ps;
ps.removeHydrides = false;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 2);
CHECK(MolOps::getFormalCharge(cp) == 1);
}
SECTION("Ferrous Hydroxide remove Hydrides") {
std::unique_ptr<RWMol> m{SmilesToMol("[Fe+2]<-[OH-]", smilesPs)};
REQUIRE(m);
MolOps::RemoveHsParameters ps;
ps.removeHydrides = true;
RWMol cp(*m);
MolOps::removeHs(cp, ps);
CHECK(cp.getNumAtoms() == 2);
CHECK(MolOps::getFormalCharge(cp) == 1);
}
SECTION("Remove All Hs in Hydrides Ferrous Hydride") {
std::unique_ptr<RWMol> m{SmilesToMol("[Fe+2]<-[H-]", smilesPs)};
REQUIRE(m);
RWMol cp(*m);
MolOps::removeAllHs(cp);
CHECK(cp.getNumAtoms() == 1);
CHECK(MolOps::getFormalCharge(cp) == 2);
}
SECTION("Remove All Hs in Hydrides Water") {
std::unique_ptr<RWMol> m{SmilesToMol("[OH+][H-]", smilesPs)};
REQUIRE(m);
RWMol cp(*m);
MolOps::removeAllHs(cp);
CHECK(cp.getNumAtoms() == 1);
CHECK(MolOps::getFormalCharge(cp) == 1);
}
}
TEST_CASE("hybridization of unknown atom types", "[bug][molops]") {
SECTION("Basics") {
auto m = "[U][U][U]"_smiles;
REQUIRE(m);
for (const auto atom : m->atoms()) {
CHECK(atom->getHybridization() == Atom::HybridizationType::S);
}
}
SECTION("comprehensive") {
std::string smiles = "";
for (unsigned int i = 89; i <= 118; ++i) {
smiles += (boost::format("[#%d]") % i).str();
}
std::unique_ptr<ROMol> m(SmilesToMol(smiles));
REQUIRE(m);
for (const auto atom : m->atoms()) {
CHECK(atom->getHybridization() == Atom::HybridizationType::S);
}
}
}
TEST_CASE("Github #3470: Hydrogen is incorrectly identified as an early atom",
"[bug][chemistry]") {
SECTION("Basics") {
RWMol m;
m.addAtom(new Atom(1), true, true);
m.getAtomWithIdx(0)->setFormalCharge(-1);
m.updatePropertyCache();
CHECK(m.getAtomWithIdx(0)->getNumImplicitHs() == 0);
m.getAtomWithIdx(0)->setFormalCharge(1);
m.updatePropertyCache();
CHECK(m.getAtomWithIdx(0)->getNumImplicitHs() == 0);
m.getAtomWithIdx(0)->setFormalCharge(0);
m.updatePropertyCache();
CHECK(m.getAtomWithIdx(0)->getNumImplicitHs() == 1);
// make sure we still generate errors for stupid stuff
m.getAtomWithIdx(0)->setFormalCharge(-2);
CHECK_THROWS_AS(m.updatePropertyCache(), AtomValenceException);
CHECK(m.getAtomWithIdx(0)->getNumImplicitHs() == 1);
}
SECTION("confirm with SMILES") {
RWMol m;
bool updateLabel = false;
bool takeOwnership = true;
m.addAtom(new Atom(1), updateLabel, takeOwnership);
m.getAtomWithIdx(0)->setFormalCharge(-1);
m.updatePropertyCache();
CHECK(MolToSmiles(m) == "[H-]");
m.getAtomWithIdx(0)->setFormalCharge(+1);
m.updatePropertyCache();
CHECK(MolToSmiles(m) == "[H+]");
m.getAtomWithIdx(0)->setFormalCharge(0);
m.updatePropertyCache();
CHECK(MolToSmiles(m) == "[HH]"); // ugly, but I think [H] would be worse
}
}
TEST_CASE("Additional oxidation states", "[chemistry]") {
SECTION("Basics") {
std::vector<std::string> smiles = {"F[Po](F)(F)(F)", "F[Po](F)(F)(F)(F)F",
"F[Xe](F)(F)(F)", "F[Xe](F)(F)(F)(F)F",
"F[I](F)F", "F[I](F)(F)(F)F",
"F[At](F)F", "F[At](F)(F)(F)F"};
for (const auto &smi : smiles) {
std::unique_ptr<ROMol> m(SmilesToMol(smi));
REQUIRE(m);
CHECK(m->getAtomWithIdx(1)->getNumRadicalElectrons() == 0);
}
}
}
TEST_CASE("Github #3805: radicals on [He]", "[chemistry]") {
SECTION("Basics") {
{
auto m = "[He]"_smiles;
REQUIRE(m);
CHECK(m->getAtomWithIdx(0)->getNumRadicalElectrons() == 0);
CHECK(m->getAtomWithIdx(0)->getTotalNumHs() == 0);
}
{
auto m = "[Ne]"_smiles;
REQUIRE(m);
CHECK(m->getAtomWithIdx(0)->getNumRadicalElectrons() == 0);
CHECK(m->getAtomWithIdx(0)->getTotalNumHs() == 0);
}
}
SECTION("Basics") {
{
auto m = "[He+]"_smiles;
REQUIRE(m);
CHECK(m->getAtomWithIdx(0)->getNumRadicalElectrons() == 1);
CHECK(m->getAtomWithIdx(0)->getTotalNumHs() == 0);
}
{
auto m = "[Ne+]"_smiles;
REQUIRE(m);
CHECK(m->getAtomWithIdx(0)->getNumRadicalElectrons() == 1);
CHECK(m->getAtomWithIdx(0)->getTotalNumHs() == 0);
}
}
}
TEST_CASE("needsHs function", "[chemistry]") {
SECTION("basics") {
const auto m = "CC"_smiles;
REQUIRE(m);
CHECK(MolOps::needsHs(*m));
// add a single H:
bool updateLabel = false;
bool takeOwnership = true;
m->addAtom(new Atom(1), updateLabel, takeOwnership);
m->addBond(0, 2, Bond::BondType::SINGLE);
MolOps::sanitizeMol(*m);
CHECK(MolOps::needsHs(*m));
// now add all the Hs:
MolOps::addHs(*m);
CHECK(!MolOps::needsHs(*m));
}
SECTION("radical") {
const auto m = "[O][O]"_smiles;
REQUIRE(m);
CHECK(!MolOps::needsHs(*m));
}
SECTION("none needed") {
const auto m = "FF"_smiles;
REQUIRE(m);
CHECK(!MolOps::needsHs(*m));
}
}
TEST_CASE(
"github #3330: incorrect number of radicals electrons calculated for "
"metals",
"[chemistry][metals]") {
SECTION("basics") {
std::vector<std::pair<std::string, unsigned int>> data = {
{"[Mn+2]", 1}, {"[Mn+1]", 0}, {"[Mn]", 1}, {"[Mn-1]", 0},
{"[C]", 4}, {"[C+1]", 3}, {"[C-1]", 3}};
for (const auto &pr : data) {
std::unique_ptr<ROMol> m(SmilesToMol(pr.first));
REQUIRE(m);
CHECK(m->getAtomWithIdx(0)->getNumRadicalElectrons() == pr.second);
}
}
}
TEST_CASE("github #3879: bad H coordinates on fused rings", "[addhs]") {
SECTION("reported") {
auto m = R"CTAB(
RDKit 2D
0 0 0 0 0 0 0 0 0 0999 V3000
M V30 BEGIN CTAB
M V30 COUNTS 9 10 0 0 0
M V30 BEGIN ATOM
M V30 1 C 1.500000 2.598076 0.000000 0
M V30 2 N 0.750000 1.299038 0.000000 0
M V30 3 C 1.500000 -0.000000 0.000000 0
M V30 4 C 0.750000 -1.299038 0.000000 0
M V30 5 C 0.382772 -0.562069 0.000000 0
M V30 6 C -0.295379 0.612525 0.000000 0
M V30 7 C -0.750000 1.299038 0.000000 0
M V30 8 C -1.500000 0.000000 0.000000 0
M V30 9 O -0.750000 -1.299038 0.000000 0
M V30 END ATOM
M V30 BEGIN BOND
M V30 1 1 1 2
M V30 2 1 2 3
M V30 3 1 4 3 CFG=3
M V30 4 1 4 5
M V30 5 1 5 6
M V30 6 1 7 6 CFG=3
M V30 7 1 7 8
M V30 8 1 8 9
M V30 9 1 7 2
M V30 10 1 9 4
M V30 END BOND
M V30 END CTAB
M END)CTAB"_ctab;
REQUIRE(m);
bool explicitOnly = false;
bool addCoords = true;
UINT_VECT onlyOnAtoms = {3, 6};
MolOps::addHs(*m, explicitOnly, addCoords, &onlyOnAtoms);
const auto &conf = m->getConformer();
// check that the H atoms bisect the angle correctly
{
REQUIRE(m->getAtomWithIdx(9)->getAtomicNum() == 1);
REQUIRE(m->getBondBetweenAtoms(9, 3));
REQUIRE(m->getBondBetweenAtoms(3, 4));
REQUIRE(m->getBondBetweenAtoms(3, 2));
REQUIRE(m->getBondBetweenAtoms(3, 8));
auto v1 = conf.getAtomPos(9) - conf.getAtomPos(3);
auto v2 = conf.getAtomPos(4) - conf.getAtomPos(3);
auto v3 = conf.getAtomPos(2) - conf.getAtomPos(3);
auto v4 = conf.getAtomPos(8) - conf.getAtomPos(3);
CHECK(v1.angleTo(v3) < v1.angleTo(v2));
CHECK(v1.angleTo(v4) < v1.angleTo(v2));
CHECK(fabs(v1.angleTo(v3) - v1.angleTo(v4)) < 1e-4);
CHECK(v1.dotProduct(v3) < -1e-4);
CHECK(v1.dotProduct(v4) < -1e-4);
}
{
REQUIRE(m->getAtomWithIdx(10)->getAtomicNum() == 1);
REQUIRE(m->getBondBetweenAtoms(10, 6));
REQUIRE(m->getBondBetweenAtoms(5, 6));
REQUIRE(m->getBondBetweenAtoms(6, 1));
REQUIRE(m->getBondBetweenAtoms(6, 7));
auto v1 = conf.getAtomPos(10) - conf.getAtomPos(6);
auto v2 = conf.getAtomPos(5) - conf.getAtomPos(6);
auto v3 = conf.getAtomPos(1) - conf.getAtomPos(6);
auto v4 = conf.getAtomPos(7) - conf.getAtomPos(6);
CHECK(v1.angleTo(v3) < v1.angleTo(v2));
CHECK(v1.angleTo(v4) < v1.angleTo(v2));
CHECK(fabs(v1.angleTo(v3) - v1.angleTo(v4)) < 1e-4);
CHECK(v1.dotProduct(v3) < -1e-4);
CHECK(v1.dotProduct(v4) < -1e-4);
}
}
SECTION("non-chiral version") {
auto m = R"CTAB(
RDKit 2D
0 0 0 0 0 0 0 0 0 0999 V3000
M V30 BEGIN CTAB
M V30 COUNTS 9 10 0 0 0
M V30 BEGIN ATOM
M V30 1 C 1.500000 2.598076 0.000000 0
M V30 2 N 0.750000 1.299038 0.000000 0
M V30 3 C 1.500000 -0.000000 0.000000 0
M V30 4 C 0.750000 -1.299038 0.000000 0
M V30 5 C 0.382772 -0.562069 0.000000 0
M V30 6 C -0.295379 0.612525 0.000000 0
M V30 7 C -0.750000 1.299038 0.000000 0
M V30 8 C -1.500000 0.000000 0.000000 0
M V30 9 O -0.750000 -1.299038 0.000000 0
M V30 END ATOM
M V30 BEGIN BOND
M V30 1 1 1 2
M V30 2 1 2 3
M V30 3 1 4 3
M V30 4 1 4 5
M V30 5 1 5 6
M V30 6 1 7 6
M V30 7 1 7 8
M V30 8 1 8 9
M V30 9 1 7 2
M V30 10 1 9 4
M V30 END BOND
M V30 END CTAB
M END)CTAB"_ctab;
REQUIRE(m);
bool explicitOnly = false;
bool addCoords = true;
UINT_VECT onlyOnAtoms = {3, 6};
MolOps::addHs(*m, explicitOnly, addCoords, &onlyOnAtoms);
const auto &conf = m->getConformer();
{
REQUIRE(m->getAtomWithIdx(9)->getAtomicNum() == 1);
REQUIRE(m->getBondBetweenAtoms(9, 3));
REQUIRE(m->getBondBetweenAtoms(3, 4));
REQUIRE(m->getBondBetweenAtoms(3, 2));
REQUIRE(m->getBondBetweenAtoms(3, 8));
auto v1 = conf.getAtomPos(9) - conf.getAtomPos(3);
auto v2 = conf.getAtomPos(4) - conf.getAtomPos(3);
auto v3 = conf.getAtomPos(2) - conf.getAtomPos(3);
auto v4 = conf.getAtomPos(8) - conf.getAtomPos(3);
CHECK(v1.angleTo(v3) < v1.angleTo(v2));
CHECK(v1.angleTo(v4) < v1.angleTo(v2));
CHECK(fabs(v1.angleTo(v3) - v1.angleTo(v4)) < 1e-4);
CHECK(v1.dotProduct(v3) < -1e-4);
CHECK(v1.dotProduct(v4) < -1e-4);
}
{
REQUIRE(m->getAtomWithIdx(10)->getAtomicNum() == 1);
REQUIRE(m->getBondBetweenAtoms(10, 6));
REQUIRE(m->getBondBetweenAtoms(5, 6));
REQUIRE(m->getBondBetweenAtoms(6, 1));
REQUIRE(m->getBondBetweenAtoms(6, 7));
auto v1 = conf.getAtomPos(10) - conf.getAtomPos(6);
auto v2 = conf.getAtomPos(5) - conf.getAtomPos(6);
auto v3 = conf.getAtomPos(1) - conf.getAtomPos(6);
auto v4 = conf.getAtomPos(7) - conf.getAtomPos(6);
CHECK(v1.angleTo(v3) < v1.angleTo(v2));
CHECK(v1.angleTo(v4) < v1.angleTo(v2));
CHECK(fabs(v1.angleTo(v3) - v1.angleTo(v4)) < 1e-4);
CHECK(v1.dotProduct(v3) < -1e-4);
CHECK(v1.dotProduct(v4) < -1e-4);
}
}
SECTION("a simpler system") {
auto m = R"CTAB(
Mrv2014 03092106042D
0 0 0 0 0 999 V3000
M V30 BEGIN CTAB
M V30 COUNTS 5 6 0 0 0
M V30 BEGIN ATOM
M V30 1 C -4.3533 6.6867 0 0
M V30 2 C -4.3533 5.1467 0 0 CFG=1
M V30 3 O -2.8133 6.6867 0 0
M V30 4 C -2.8133 5.1467 0 0 CFG=1
M V30 5 C -3.5833 3.813 0 0
M V30 END ATOM
M V30 BEGIN BOND
M V30 1 1 1 3
M V30 2 1 2 4
M V30 3 1 3 4
M V30 4 1 2 5
M V30 5 1 4 5 CFG=1
M V30 6 1 2 1 CFG=1
M V30 END BOND
M V30 END CTAB
M END
)CTAB"_ctab;
bool explicitOnly = false;
bool addCoords = true;
UINT_VECT onlyOnAtoms = {3, 1};
MolOps::addHs(*m, explicitOnly, addCoords, &onlyOnAtoms);
const auto &conf = m->getConformer();
{
REQUIRE(m->getAtomWithIdx(5)->getAtomicNum() == 1);
REQUIRE(m->getBondBetweenAtoms(5, 1));
REQUIRE(m->getBondBetweenAtoms(1, 3));
REQUIRE(m->getBondBetweenAtoms(1, 0));
REQUIRE(m->getBondBetweenAtoms(1, 4));
auto v1 = conf.getAtomPos(5) - conf.getAtomPos(1);
auto v2 = conf.getAtomPos(3) - conf.getAtomPos(1);
auto v3 = conf.getAtomPos(0) - conf.getAtomPos(1);
auto v4 = conf.getAtomPos(4) - conf.getAtomPos(1);
CHECK(v1.angleTo(v3) < v1.angleTo(v2));
CHECK(v1.angleTo(v4) < v1.angleTo(v2));
CHECK(fabs(v1.angleTo(v3) - v1.angleTo(v4)) < 1e-4);
CHECK(v1.dotProduct(v3) < -1e-4);
CHECK(v1.dotProduct(v4) < -1e-4);
}
}
SECTION("#3932: followup from #3879") {
auto m = R"CTAB(
RDKit 2D
21 22 0 0 0 0 0 0 0 0999 V2000
-6.9959 0.0617 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.5212 0.3365 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.0219 1.7509 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-4.5460 -0.8032 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.0713 -0.5284 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.0961 -1.6681 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.6214 -1.3933 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.2270 -0.1562 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.4640 -1.0046 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
2.6531 -0.0903 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.0918 -0.5150 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1788 0.5186 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.4434 -1.9732 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.1510 1.3231 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.6092 1.6747 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.9538 2.8101 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.6516 1.2824 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
0.7678 2.7779 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.8236 1.5543 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.6156 -2.2417 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.8904 -3.7163 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0
2 3 2 0
2 4 1 0
4 5 2 0
5 6 1 0
6 7 1 0
8 7 1 6
8 9 1 0
9 10 1 0
10 11 1 6
11 12 2 0
11 13 1 0
10 14 1 0
14 15 1 0
14 16 1 0
14 17 1 0
17 18 2 0
17 19 2 0
9 20 1 0
20 21 2 0
20 7 1 0
17 8 1 0
M END)CTAB"_ctab;
REQUIRE(m);
bool explicitOnly = false;
bool addCoords = true;
UINT_VECT onlyOnAtoms = {7};
MolOps::addHs(*m, explicitOnly, addCoords, &onlyOnAtoms);
const auto &conf = m->getConformer();
{
REQUIRE(m->getAtomWithIdx(21)->getAtomicNum() == 1);
REQUIRE(m->getBondBetweenAtoms(21, 7));
REQUIRE(m->getBondBetweenAtoms(7, 8));
REQUIRE(m->getBondBetweenAtoms(7, 16));
REQUIRE(m->getBondBetweenAtoms(7, 6));
auto v1 = conf.getAtomPos(21) - conf.getAtomPos(7);
auto v2 = conf.getAtomPos(6) - conf.getAtomPos(7);
auto v3 = conf.getAtomPos(16) - conf.getAtomPos(7);
auto v4 = conf.getAtomPos(8) - conf.getAtomPos(7);
CHECK(v1.angleTo(v2) < v1.angleTo(v4));
CHECK(v1.angleTo(v3) < v1.angleTo(v4));
CHECK(fabs(v1.angleTo(v2) - v1.angleTo(v3)) < 1e-4);
}
}
}
TEST_CASE("batch edits", "[editing]") {
SECTION("removeAtom") {
auto m = "C1CCCO1"_smiles;
REQUIRE(m);
m->beginBatchEdit();
m->removeAtom(2);
m->removeAtom(3);
m->commitBatchEdit();
CHECK(MolToSmiles(*m) == "CCO");
}
SECTION("removeAtom + removeBond") {
auto m = "C1CCCO1"_smiles;
REQUIRE(m);
m->beginBatchEdit();
m->removeAtom(3);
m->removeBond(4, 0);
m->commitBatchEdit();
CHECK(MolToSmiles(*m) == "CCC.O");
}
SECTION("rollback") {
auto m = "C1CCCO1"_smiles;
REQUIRE(m);
m->beginBatchEdit();
m->removeAtom(2);
m->removeAtom(3);
m->rollbackBatchEdit();
CHECK(MolToSmiles(*m) == "C1CCOC1");
}
SECTION("adding atoms while in a batch") {
auto m = "CCCO"_smiles;
REQUIRE(m);
m->beginBatchEdit();
m->removeAtom(2);
bool updateLabel = false;
bool takeOwnership = true;
m->addAtom(new Atom(7), updateLabel, takeOwnership);
m->removeAtom(1);
m->commitBatchEdit();
CHECK(MolToSmiles(*m) == "C.N.O");
}
SECTION("removing added atoms while in a batch") {
auto m = "CCCO"_smiles;
REQUIRE(m);
m->beginBatchEdit();
m->removeAtom(2);
bool updateLabel = false;
bool takeOwnership = true;
m->addAtom(new Atom(7), updateLabel, takeOwnership);
m->removeAtom(4);
m->commitBatchEdit();
CHECK(MolToSmiles(*m) == "CC.O");
}
SECTION("adding bonds while in a batch") {
auto m = "CCCO"_smiles;
REQUIRE(m);
m->beginBatchEdit();
m->removeBond(2, 3);
m->addBond(0, 3, Bond::BondType::SINGLE);
m->commitBatchEdit();
CHECK(MolToSmiles(*m) == "CCCO");
}
SECTION("removing added bonds while in a batch") {
auto m = "CCCO"_smiles;
REQUIRE(m);
m->beginBatchEdit();
m->addBond(0, 3, Bond::BondType::SINGLE);
m->removeBond(2, 3);
m->removeBond(0, 3);
m->commitBatchEdit();
CHECK(MolToSmiles(*m) == "CCC.O");
}
SECTION("some details") {
auto m = "CCCO"_smiles;
REQUIRE(m);
m->beginBatchEdit();
CHECK_THROWS_AS(m->beginBatchEdit(), ValueErrorException);
m->removeAtom(0U);
// copying includes the edit status:
RWMol m2(*m);
CHECK_THROWS_AS(m2.beginBatchEdit(), ValueErrorException);
// without a commit, the mols haven't changed
CHECK(MolToSmiles(*m) == "CCCO");
CHECK(MolToSmiles(m2) == "CCCO");
m->commitBatchEdit();
CHECK(MolToSmiles(*m) == "CCO");
m2.commitBatchEdit();
CHECK(MolToSmiles(m2) == "CCO");
}
}
TEST_CASE("github #4122: segfaults in commitBatchEdit()", "[editing]][bug]") {
SECTION("as reported, no atoms") {
RWMol m;
m.beginBatchEdit();
m.addAtom();
m.commitBatchEdit();
}
SECTION("no bonds") {
auto m = "C.C"_smiles;
m->beginBatchEdit();
m->addBond(0, 1, Bond::BondType::SINGLE);
m->commitBatchEdit();
}
SECTION("after add atom") {
auto m = "CC"_smiles;
m->beginBatchEdit();
m->addAtom(6);
m->removeAtom(0u);
m->addAtom(6);
m->commitBatchEdit();
}
SECTION("remove a just-added atom") {
auto m = "CC"_smiles;
m->beginBatchEdit();
m->addAtom(6);
m->removeAtom(2);
m->commitBatchEdit();
}
}
TEST_CASE("github #3912: cannot draw atom lists from SMARTS", "[query][bug]") {
SECTION("original") {
auto m = "C(-[N,O])-[#7,#8]"_smarts;
REQUIRE(m);
CHECK(isAtomListQuery(m->getAtomWithIdx(1)));
CHECK(isAtomListQuery(m->getAtomWithIdx(2)));
std::vector<int> vals;
getAtomListQueryVals(m->getAtomWithIdx(2)->getQuery(), vals);
CHECK(vals == std::vector<int>{7, 8});
vals.clear();
getAtomListQueryVals(m->getAtomWithIdx(1)->getQuery(), vals);
CHECK(vals == std::vector<int>{7, 8});
}
}
TEST_CASE("github #4496: cannot draw aromatic atom lists from SMARTS",
"[query][bug]") {
SECTION("original") {
auto m = "[c,n]1[c,n][c,n][c,n][c,n][c,n]1"_smarts;
REQUIRE(m);
std::vector<int> expected({6, 7});
for (const auto a : m->atoms()) {
CHECK(isAtomListQuery(a));
std::vector<int> vals;
getAtomListQueryVals(a->getQuery(), vals);
CHECK(vals == expected);
}
}
}
TEST_CASE("bridgehead queries", "[query]") {
SECTION("basics") {
{
auto m = "CC12CCN(CC1)C2"_smiles;
REQUIRE(m);
for (const auto atom : m->atoms()) {
auto test = queryIsAtomBridgehead(atom);
if (atom->getIdx() == 1 || atom->getIdx() == 4) {
CHECK(test == 1);
} else {
CHECK(test == 0);
}
}
}
{
auto m = "CC12CCC(C)(CC1)CC2"_smiles;
REQUIRE(m);
for (const auto atom : m->atoms()) {
auto test = queryIsAtomBridgehead(atom);
if (atom->getIdx() == 1 || atom->getIdx() == 4) {
CHECK(test == 1);
} else {
CHECK(test == 0);
}
}
}
{ // no bridgehead
auto m = "C1CCC2CCCCC2C1"_smiles;
REQUIRE(m);
for (const auto atom : m->atoms()) {
auto test = queryIsAtomBridgehead(atom);
CHECK(test == 0);
}
}
}
}
TEST_CASE("replaceAtom/Bond should not screw up bookmarks", "[RWMol]") {
SECTION("atom basics") {
auto m = "CCC"_smiles;
REQUIRE(m);
m->setAtomBookmark(m->getAtomWithIdx(2), 1);
auto origAt2 = m->getAtomWithIdx(2);
CHECK(m->getUniqueAtomWithBookmark(1) == origAt2);
Atom O(8);
m->replaceAtom(2, &O);
auto at2 = m->getAtomWithIdx(2);
CHECK(at2 != origAt2);
CHECK(m->getUniqueAtomWithBookmark(1) == at2);
}
SECTION("bond basics") {
auto m = "CCCC"_smiles;
REQUIRE(m);
m->setBondBookmark(m->getBondWithIdx(2), 1);
auto origB2 = m->getBondWithIdx(2);
CHECK(m->getUniqueBondWithBookmark(1) == origB2);
Bond single(Bond::BondType::SINGLE);
m->replaceBond(2, &single);
auto b2 = m->getBondWithIdx(2);
CHECK(b2 != origB2);
CHECK(m->getUniqueBondWithBookmark(1) == b2);
}
}
TEST_CASE("github #4071: StereoGroups not preserved by RenumberAtoms()",
"[molops]") {
SECTION("basics") {
auto mol =
"C[C@@H](O)[C@H](C)[C@@H](C)[C@@H](C)O |&3:3,o1:7,&1:1,&2:5,r|"_smiles;
REQUIRE(mol);
REQUIRE(mol->getStereoGroups().size() == 4);
std::vector<unsigned int> aindices(mol->getNumAtoms());
std::iota(aindices.begin(), aindices.end(), 0);
std::reverse(aindices.begin(), aindices.end());
std::unique_ptr<ROMol> nmol(MolOps::renumberAtoms(*mol, aindices));
REQUIRE(nmol);
CHECK(nmol->getStereoGroups().size() == 4);
for (size_t i = 0; i < nmol->getStereoGroups().size(); ++i) {
CHECK(nmol->getStereoGroups()[i].getGroupType() ==
mol->getStereoGroups()[i].getGroupType());
}
CHECK(MolToCXSmiles(*nmol) ==
"C[C@@H](O)[C@H](C)[C@@H](C)[C@@H](C)O |o1:1,&1:3,&2:5,&3:7|");
}
}
TEST_CASE("github #4127: SEGV in ROMol::getAtomDegree if atom is not in graph",
"[graphmol]") {
// also includes tests for some related edge cases found as part of that bug
// fix
Atom atom(6);
RWMol mol1;
auto mol2 = "CCC"_smiles;
SECTION("getAtomDegree") {
CHECK_THROWS_AS(mol1.getAtomDegree(nullptr), Invar::Invariant);
CHECK_THROWS_AS(mol1.getAtomDegree(&atom), Invar::Invariant);
CHECK_THROWS_AS(mol1.getAtomDegree(mol2->getAtomWithIdx(0)),
Invar::Invariant);
}
SECTION("getAtomNeighbors") {
CHECK_THROWS_AS(mol1.getAtomNeighbors(nullptr), Invar::Invariant);
CHECK_THROWS_AS(mol1.getAtomNeighbors(&atom), Invar::Invariant);
CHECK_THROWS_AS(mol1.getAtomNeighbors(mol2->getAtomWithIdx(0)),
Invar::Invariant);
}
SECTION("getAtomBonds") {
CHECK_THROWS_AS(mol1.getAtomBonds(nullptr), Invar::Invariant);
CHECK_THROWS_AS(mol1.getAtomBonds(&atom), Invar::Invariant);
CHECK_THROWS_AS(mol1.getAtomBonds(mol2->getAtomWithIdx(0)),
Invar::Invariant);
}
SECTION("addAtom from another molecule") {
RWMol mol1cp(mol1);
CHECK_THROWS_AS(mol1cp.addAtom(nullptr), Invar::Invariant);
bool updateLabel = false;
bool takeOwnership = true;
CHECK_THROWS_AS(
mol1cp.addAtom(mol2->getAtomWithIdx(0), updateLabel, takeOwnership),
Invar::Invariant);
takeOwnership = false;
CHECK(mol1cp.addAtom(mol2->getAtomWithIdx(0), updateLabel, takeOwnership) ==
0);
}
SECTION("addBond from another molecule") {
auto mol3 = "C.C.C"_smiles;
bool takeOwnership = true;
CHECK_THROWS_AS(mol3->addBond(mol2->getBondWithIdx(0), takeOwnership),
Invar::Invariant);
takeOwnership = false;
CHECK(mol3->addBond(mol2->getBondWithIdx(0), takeOwnership) == 1);
}
}
TEST_CASE(
"github #4128: SEGV from unsigned integer overflow in "
"Conformer::setAtomPos",
"[graphmol]") {
Conformer conf;
RDGeom::Point3D pt(0, 0, 0);
CHECK_THROWS_AS(conf.setAtomPos(std::numeric_limits<unsigned>::max(), pt),
ValueErrorException);
}
TEST_CASE("KekulizeFragment", "[graphmol]") {
SECTION("basics") {
auto mol = "CCc1ccccc1"_smiles;
REQUIRE(mol);
boost::dynamic_bitset<> atomsInPlay(mol->getNumAtoms());
for (auto aidx : std::vector<size_t>{0, 1, 2, 3}) {
atomsInPlay.set(aidx);
}
boost::dynamic_bitset<> bondsInPlay(mol->getNumBonds());
for (auto bidx : std::vector<size_t>{0, 1, 2}) {
bondsInPlay.set(bidx);
}
MolOps::details::KekulizeFragment(*mol, atomsInPlay, bondsInPlay);
CHECK(!mol->getAtomWithIdx(2)->getIsAromatic());
CHECK(mol->getAtomWithIdx(4)->getIsAromatic());
CHECK(!mol->getBondWithIdx(2)->getIsAromatic());
// at the moment that bond still has an aromatic bond order, which isn't
// optimal, but that will have to wait until we add a feature to allow
// kekulization of conjugated chains.
CHECK(mol->getBondWithIdx(2)->getBondType() == Bond::AROMATIC);
CHECK(mol->getBondWithIdx(4)->getIsAromatic());
}
}
TEST_CASE(
"github #4266: fallback ring finding failing on molecules with multiple "
"fragments",
"[graphmol]") {
SECTION("case1") {
auto m = "C123C45C16C21C34C561.c1ccccc1"_smiles;
REQUIRE(m);
ROMol m2(*m);
m2.getRingInfo()->reset();
MolOps::fastFindRings(m2);
CHECK(m->getRingInfo()->numRings() == m2.getRingInfo()->numRings());
}
SECTION("case2") {
auto m = "c1ccccc1.C123C45C16C21C34C561"_smiles;
REQUIRE(m);
ROMol m2(*m);
m2.getRingInfo()->reset();
MolOps::fastFindRings(m2);
CHECK(m->getRingInfo()->numRings() == m2.getRingInfo()->numRings());
}
}
TEST_CASE("QueryBond valence contribs") {
{
auto m = "CO"_smarts;
REQUIRE(m);
CHECK(m->getBondWithIdx(0)->getValenceContrib(m->getAtomWithIdx(0)) == 0.0);
CHECK(m->getBondWithIdx(0)->getValenceContrib(m->getAtomWithIdx(1)) == 0.0);
}
{
auto m = "C-O"_smarts;
REQUIRE(m);
CHECK(m->getBondWithIdx(0)->getValenceContrib(m->getAtomWithIdx(0)) == 1.0);
CHECK(m->getBondWithIdx(0)->getValenceContrib(m->getAtomWithIdx(1)) == 1.0);
}
}
TEST_CASE(
"github #4311: unreasonable calculation of implicit valence for atoms with "
"query bonds",
"[graphmol]") {
SECTION("basics") {
auto m = "C-,=O"_smarts;
REQUIRE(m);
m->updatePropertyCache();
CHECK(m->getAtomWithIdx(0)->getTotalNumHs() == 0);
CHECK(m->getAtomWithIdx(1)->getTotalNumHs() == 0);
CHECK(MolToSmiles(*m) == "CO");
CHECK(MolToSmarts(*m) == "C-,=O");
}
}
TEST_CASE("atom copy ctor") {
auto m = "CO"_smiles;
REQUIRE(m);
for (const auto atom : m->atoms()) {
Atom cp(*atom);
CHECK(cp.getAtomicNum() == atom->getAtomicNum());
CHECK(!cp.hasOwningMol());
}
}
TEST_CASE("bond copy ctor") {
auto m = "COC"_smiles;
REQUIRE(m);
for (const auto bond : m->bonds()) {
Bond cp(*bond);
CHECK(cp.getBondType() == bond->getBondType());
CHECK(!cp.hasOwningMol());
}
}
TEST_CASE("valence edge") {
{ // this is, of course, absurd:
auto m = "[H-2]"_smiles;
REQUIRE(m);
m->getAtomWithIdx(0)->setNoImplicit(false);
m->updatePropertyCache(false);
CHECK(m->getAtomWithIdx(0)->getFormalCharge() == -2);
CHECK(m->getAtomWithIdx(0)->getImplicitValence() == 0);
}
{
SmilesParserParams ps;
ps.sanitize = false;
std::unique_ptr<RWMol> m{SmilesToMol("CFC", ps)};
REQUIRE(m);
CHECK_THROWS_AS(m->getAtomWithIdx(1)->calcImplicitValence(true),
AtomValenceException);
}
}
TEST_CASE("SetQuery on normal atoms") {
auto m = "CC"_smiles;
REQUIRE(m);
auto qry = makeAtomAliphaticQuery();
CHECK_THROWS_AS(m->getAtomWithIdx(0)->setQuery(qry), std::runtime_error);
CHECK_THROWS_AS(m->getAtomWithIdx(0)->expandQuery(qry), std::runtime_error);
delete qry;
}
TEST_CASE("SetQuery on normal bonds") {
auto m = "CC"_smiles;
REQUIRE(m);
auto qry = makeBondOrderEqualsQuery(Bond::BondType::SINGLE);
CHECK_THROWS_AS(m->getBondWithIdx(0)->setQuery(qry), std::runtime_error);
CHECK_THROWS_AS(m->getBondWithIdx(0)->expandQuery(qry), std::runtime_error);
delete qry;
}
TEST_CASE("additional atom props") {
auto m = "CC"_smiles;
REQUIRE(m);
auto atom = m->getAtomWithIdx(0);
{
CHECK(!atom->hasProp(common_properties::_MolFileRLabel));
setAtomRLabel(atom, 1);
CHECK(atom->hasProp(common_properties::_MolFileRLabel));
setAtomRLabel(atom, 0);
CHECK(!atom->hasProp(common_properties::_MolFileRLabel));
}
{
CHECK(!atom->hasProp(common_properties::molFileAlias));
setAtomAlias(atom, "foo");
CHECK(atom->hasProp(common_properties::molFileAlias));
setAtomAlias(atom, "");
CHECK(!atom->hasProp(common_properties::molFileAlias));
}
{
CHECK(!atom->hasProp(common_properties::molFileValue));
setAtomValue(atom, "foo");
CHECK(atom->hasProp(common_properties::molFileValue));
setAtomValue(atom, "");
CHECK(!atom->hasProp(common_properties::molFileValue));
}
{
CHECK(!atom->hasProp(common_properties::_supplementalSmilesLabel));
setSupplementalSmilesLabel(atom, "foo");
CHECK(atom->hasProp(common_properties::_supplementalSmilesLabel));
setSupplementalSmilesLabel(atom, "");
CHECK(!atom->hasProp(common_properties::_supplementalSmilesLabel));
}
}
TEST_CASE("getBondTypeAsDouble()") {
SECTION("plain") {
std::vector<std::pair<Bond::BondType, double>> vals{
{Bond::BondType::IONIC, 0},
{Bond::BondType::ZERO, 0},
{Bond::BondType::SINGLE, 1},
{Bond::BondType::DOUBLE, 2},
{Bond::BondType::TRIPLE, 3},
{Bond::BondType::QUADRUPLE, 4},
{Bond::BondType::QUINTUPLE, 5},
{Bond::BondType::HEXTUPLE, 6},
{Bond::BondType::ONEANDAHALF, 1.5},
{Bond::BondType::TWOANDAHALF, 2.5},
{Bond::BondType::THREEANDAHALF, 3.5},
{Bond::BondType::FOURANDAHALF, 4.5},
{Bond::BondType::FIVEANDAHALF, 5.5},
{Bond::BondType::AROMATIC, 1.5},
{Bond::BondType::DATIVEONE, 1.0},
{Bond::BondType::DATIVE, 1.0},
{Bond::BondType::HYDROGEN, 0}
};
for (const auto &pr : vals) {
Bond bnd(pr.first);
CHECK(bnd.getBondType() == pr.first);
CHECK(bnd.getBondTypeAsDouble() == pr.second);
}
}
SECTION("twice") {
std::vector<std::pair<Bond::BondType, std::uint8_t>> vals{
{Bond::BondType::IONIC, 0}, {Bond::BondType::ZERO, 0},
{Bond::BondType::SINGLE, 2}, {Bond::BondType::DOUBLE, 4},
{Bond::BondType::TRIPLE, 6}, {Bond::BondType::QUADRUPLE, 8},
{Bond::BondType::QUINTUPLE, 10}, {Bond::BondType::HEXTUPLE, 12},
{Bond::BondType::ONEANDAHALF, 3}, {Bond::BondType::TWOANDAHALF, 5},
{Bond::BondType::THREEANDAHALF, 7}, {Bond::BondType::FOURANDAHALF, 9},
{Bond::BondType::FIVEANDAHALF, 11}, {Bond::BondType::AROMATIC, 3},
{Bond::BondType::DATIVEONE, 2}, {Bond::BondType::DATIVE, 2},
{Bond::BondType::HYDROGEN, 0}
};
for (const auto &pr : vals) {
Bond bnd(pr.first);
CHECK(bnd.getBondType() == pr.first);
CHECK(getTwiceBondType(bnd) == pr.second);
}
}
}
TEST_CASE("getValenceContrib()") {
const auto m = "CO->[Fe]"_smiles;
REQUIRE(m);
CHECK(m->getBondWithIdx(1)->getValenceContrib(m->getAtomWithIdx(0)) == 0);
CHECK(m->getBondWithIdx(1)->getValenceContrib(m->getAtomWithIdx(1)) == 0);
CHECK(m->getBondWithIdx(1)->getValenceContrib(m->getAtomWithIdx(2)) == 1);
}
TEST_CASE("conformer details") {
const auto m = "CC"_smiles;
REQUIRE(m);
Conformer *conf = new Conformer(m->getNumAtoms());
CHECK(!conf->hasOwningMol());
m->addConformer(conf);
CHECK(conf->hasOwningMol());
auto cid = conf->getId();
*conf = *conf;
CHECK(conf->hasOwningMol());
CHECK(conf->getId() == cid);
}
#if !defined(_WIN32) || !defined(RDKIT_DYN_LINK)
namespace RDKit {
namespace Canon {
namespace details {
bool atomHasFourthValence(const Atom *atom);
bool hasSingleHQuery(const Atom::QUERYATOM_QUERY *q);
} // namespace details
void switchBondDir(Bond *bond);
} // namespace Canon
} // namespace RDKit
TEST_CASE("canon details") {
SECTION("h queries") {
std::vector<std::pair<std::string, bool>> examples{
{"C[CHD3](F)Cl", true}, {"C[CD3H](F)Cl", true},
{"C[CH3D](F)Cl", false}, {"C[CDH3](F)Cl", false},
{"C[CDR4H](F)Cl", true},
};
for (const auto &pr : examples) {
std::unique_ptr<RWMol> m{SmartsToMol(pr.first)};
REQUIRE(m);
CHECK(RDKit::Canon::details::hasSingleHQuery(
m->getAtomWithIdx(1)->getQuery()) == pr.second);
CHECK(RDKit::Canon::details::atomHasFourthValence(m->getAtomWithIdx(1)) ==
pr.second);
// artificial, but causes atomHasFourthValence to always return true
m->getAtomWithIdx(1)->setNumExplicitHs(1);
CHECK(RDKit::Canon::details::atomHasFourthValence(m->getAtomWithIdx(1)));
}
}
}
TEST_CASE("switchBondDir") {
auto m = "C/C=C/C"_smiles;
REQUIRE(m);
auto bond = m->getBondWithIdx(0);
CHECK(bond->getBondDir() == Bond::BondDir::ENDUPRIGHT);
Canon::switchBondDir(bond);
CHECK(bond->getBondDir() == Bond::BondDir::ENDDOWNRIGHT);
bond->setBondDir(Bond::BondDir::UNKNOWN);
Canon::switchBondDir(bond);
CHECK(bond->getBondDir() == Bond::BondDir::UNKNOWN);
}
#endif
TEST_CASE("allow 5 valent N/P/As to kekulize", "[kekulization]") {
std::vector<std::pair<std::string, std::string>> tests = {
{"O=n1ccccc1", "O=N1=CC=CC=C1"},
{"O=p1ccccc1", "O=P1=CC=CC=C1"},
{"O=[as]1ccccc1", "O=[As]1=CC=CC=C1"}};
SmilesParserParams ps;
ps.sanitize = false;
SECTION("kekulization") {
for (const auto &pr : tests) {
std::unique_ptr<RWMol> m{SmilesToMol(pr.first, ps)};
REQUIRE(m);
m->updatePropertyCache(false);
MolOps::Kekulize(*m);
CHECK(MolToSmiles(*m) == pr.second);
}
}
SECTION("sanitization") {
for (const auto &pr : tests) {
std::unique_ptr<RWMol> m{SmilesToMol(pr.first, ps)};
REQUIRE(m);
m->updatePropertyCache(false);
unsigned int failed;
unsigned int flags = MolOps::SanitizeFlags::SANITIZE_ALL ^
MolOps::SanitizeFlags::SANITIZE_CLEANUP ^
MolOps::SanitizeFlags::SANITIZE_PROPERTIES;
MolOps::sanitizeMol(*m, failed, flags);
CHECK(!failed);
CHECK(MolToSmiles(*m) == pr.second);
}
}
}
TEST_CASE("KekulizeIfPossible") {
SECTION("basics: molecules with failures") {
std::vector<std::string> smis = {
"c1cccn1",
"c1ccccc1-c1cccn1",
};
for (const auto &smi : smis) {
SmilesParserParams ps;
ps.sanitize = false;
std::unique_ptr<RWMol> m{SmilesToMol(smi, ps)};
REQUIRE(m);
m->updatePropertyCache(false);
// confirm that we normally fail:
{
RWMol m2(*m);
CHECK_THROWS_AS(MolOps::Kekulize(m2), MolSanitizeException);
}
{
RWMol m2(*m);
CHECK(!MolOps::KekulizeIfPossible(m2));
for (unsigned i = 0; i < m2.getNumAtoms(); ++i) {
CHECK(m2.getAtomWithIdx(i)->getIsAromatic() ==
m->getAtomWithIdx(i)->getIsAromatic());
}
for (unsigned i = 0; i < m2.getNumBonds(); ++i) {
CHECK(m2.getBondWithIdx(i)->getIsAromatic() ==
m->getBondWithIdx(i)->getIsAromatic());
CHECK(m2.getBondWithIdx(i)->getBondType() ==
m->getBondWithIdx(i)->getBondType());
}
}
}
}
SECTION("basics: molecules without failures") {
std::vector<std::string> smis = {"c1ccc[nH]1", "c1ccccc1"};
for (const auto &smi : smis) {
SmilesParserParams ps;
ps.sanitize = false;
std::unique_ptr<RWMol> m{SmilesToMol(smi, ps)};
REQUIRE(m);
m->updatePropertyCache(false);
{
RWMol m2(*m);
MolOps::Kekulize(m2);
RWMol m3(*m);
CHECK(MolOps::KekulizeIfPossible(m3));
for (unsigned i = 0; i < m2.getNumAtoms(); ++i) {
CHECK(m2.getAtomWithIdx(i)->getIsAromatic() ==
m3.getAtomWithIdx(i)->getIsAromatic());
}
for (unsigned i = 0; i < m2.getNumBonds(); ++i) {
CHECK(m2.getBondWithIdx(i)->getIsAromatic() ==
m3.getBondWithIdx(i)->getIsAromatic());
CHECK(m2.getBondWithIdx(i)->getBondType() ==
m3.getBondWithIdx(i)->getBondType());
}
}
}
}
}
TEST_CASE("Github #4535: operator<< for AtomPDBResidue", "[PDB]") {
SECTION("basics") {
bool sanitize = true;
int flavor = 0;
std::unique_ptr<RWMol> mol(SequenceToMol("KY", sanitize, flavor));
REQUIRE(mol);
REQUIRE(mol->getAtomWithIdx(0)->getMonomerInfo());
auto res = static_cast<AtomPDBResidueInfo *>(
mol->getAtomWithIdx(0)->getMonomerInfo());
REQUIRE(res);
std::stringstream oss;
oss << *res << std::endl;
res = static_cast<AtomPDBResidueInfo *>(
mol->getAtomWithIdx(mol->getNumAtoms() - 1)->getMonomerInfo());
REQUIRE(res);
oss << *res << std::endl;
auto tgt = R"FOO(1 N LYS A 1
22 OXT TYR A 2
)FOO";
CHECK(oss.str() == tgt);
}
}
TEST_CASE("isAromaticAtom") {
SECTION("basics") {
SmilesParserParams ps;
ps.sanitize = false;
std::unique_ptr<RWMol> mol(SmilesToMol("C:C:C", ps));
REQUIRE(mol);
CHECK(!mol->getAtomWithIdx(0)->getIsAromatic());
CHECK(mol->getBondWithIdx(0)->getIsAromatic());
CHECK(isAromaticAtom(*mol->getAtomWithIdx(0)));
}
}
TEST_CASE(
"Github #4785: aromatic bonds no longer set aromatic flags on atoms") {
SECTION("basics1") {
auto m = "C1:C:C:C:1"_smiles;
REQUIRE(m);
CHECK(MolToSmiles(*m) == "C1=CC=C1");
}
SECTION("basics2") {
auto m = "C1:C:C:C:C:C:1"_smiles;
REQUIRE(m);
CHECK(MolToSmiles(*m) == "c1ccccc1");
}
SECTION("can still get kekulization errors") {
CHECK_THROWS_AS(SmilesToMol("C1:C:C:C:C:1"), KekulizeException);
}
}
namespace {
void check_dest(RWMol *m1, const ROMol &m2) {
CHECK(m2.getNumAtoms() == 8);
CHECK(m2.getNumBonds() == 7);
for (const auto atom : m2.atoms()) {
CHECK(&atom->getOwningMol() == &m2);
CHECK(&atom->getOwningMol() != m1);
}
for (const auto bond : m2.bonds()) {
CHECK(&bond->getOwningMol() == &m2);
CHECK(&bond->getOwningMol() != m1);
}
CHECK(m2.getStereoGroups().size() == 2);
CHECK(m2.getStereoGroups()[0].getAtoms().size() == 2);
CHECK(m2.getStereoGroups()[0].getAtoms()[0]->getIdx() == 1);
CHECK(m2.getStereoGroups()[0].getAtoms()[1]->getIdx() == 5);
CHECK(m2.getStereoGroups()[1].getAtoms().size() == 1);
CHECK(m2.getStereoGroups()[1].getAtoms()[0]->getIdx() == 3);
const auto &sgs = getSubstanceGroups(m2);
CHECK(sgs.size() == 1);
CHECK(sgs[0].getAtoms().size() == 1);
CHECK(sgs[0].getAtoms()[0] == 4);
// check the state of m1:
CHECK(m1->getNumAtoms() == 0);
CHECK(m1->getNumBonds() == 0);
CHECK(m1->getPropList().empty());
CHECK(m1->getDict().getData().empty());
CHECK(m1->getStereoGroups().empty());
CHECK(getSubstanceGroups(*m1).empty());
CHECK(m1->getRingInfo() == nullptr);
// make sure we can still do something with m1:
*m1 = m2;
CHECK(!m1->getDict().getData().empty());
CHECK(m1->getNumAtoms() == 8);
CHECK(m1->getNumBonds() == 7);
CHECK(m1->getRingInfo() != nullptr);
CHECK(m1->getRingInfo()->isInitialized() ==
m2.getRingInfo()->isInitialized());
}
} // namespace
TEST_CASE("moves") {
auto m1 =
"C[C@H](O)[C@H](F)[C@@H](C)O |o2:1,5,&1:3,SgD:4:atom_data:foo::::|"_smiles;
REQUIRE(m1);
CHECK(m1->getStereoGroups().size() == 2);
m1->setProp("foo", 1u);
SECTION("molecule move") {
ROMol m2 = std::move(*m1);
check_dest(m1.get(), m2);
}
SECTION("molecule move-assign") {
ROMol m2;
m2 = std::move(*m1);
check_dest(m1.get(), m2);
}
}
TEST_CASE("query moves") {
auto m1 =
"C[C@H](O)[C@H](F)[C@@H](C)O |o2:1,5,&1:3,SgD:4:atom_data:foo::::|"_smarts;
REQUIRE(m1);
CHECK(m1->getStereoGroups().size() == 2);
m1->setProp("foo", 1u);
SECTION("molecule move") {
ROMol m2 = std::move(*m1);
check_dest(m1.get(), m2);
}
SECTION("molecule move-assign") {
ROMol m2;
m2 = std::move(*m1);
check_dest(m1.get(), m2);
}
}
TEST_CASE("moves with conformer") {
auto m1 = R"CTAB(
Mrv2108 01192209042D
0 0 0 0 0 999 V3000
M V30 BEGIN CTAB
M V30 COUNTS 8 7 1 0 0
M V30 BEGIN ATOM
M V30 1 C 2.31 4.001 0 0
M V30 2 C 1.54 2.6674 0 0 CFG=2
M V30 3 O -0 2.6674 0 0
M V30 4 C 2.31 1.3337 0 0 CFG=1
M V30 5 F 3.85 1.3337 0 0
M V30 6 C 1.54 0 0 0 CFG=2
M V30 7 C 2.31 -1.3337 0 0
M V30 8 O 0 0 0 0
M V30 END ATOM
M V30 BEGIN BOND
M V30 1 1 2 1
M V30 2 1 2 3 CFG=3
M V30 3 1 4 2
M V30 4 1 4 5 CFG=1
M V30 5 1 4 6
M V30 6 1 6 7
M V30 7 1 6 8 CFG=3
M V30 END BOND
M V30 BEGIN SGROUP
M V30 1 DAT 0 ATOMS=(1 5) FIELDNAME=atom_data -
M V30 FIELDDISP=" 4.6200 0.5637 DA ALL 0 0" FIELDDATA=foo
M V30 END SGROUP
M V30 BEGIN COLLECTION
M V30 MDLV30/STEREL2 ATOMS=(2 2 6)
M V30 MDLV30/STERAC1 ATOMS=(1 4)
M V30 END COLLECTION
M V30 END CTAB
M END
)CTAB"_ctab;
REQUIRE(m1);
CHECK(m1->getStereoGroups().size() == 2);
m1->setProp("foo", 1u);
SECTION("molecule move") {
ROMol m2 = std::move(*m1);
check_dest(m1.get(), m2);
}
SECTION("molecule move-assign") {
ROMol m2;
m2 = std::move(*m1);
check_dest(m1.get(), m2);
}
}
TEST_CASE("Github #5055") {
SECTION("as reported") {
auto m =
"CC1(C)NC(=O)CN2C=C(C[C@H](C(=O)NC)NC(=O)CN3CCN(C(=O)[C@H]4Cc5c([nH]c6ccccc56)CN4C(=O)CN4CN(c5ccccc5)C5(CCN(CC5)C1=O)C4=O)[C@@H](Cc1ccccc1)C3=O)[N-][NH2+]2"_smiles;
REQUIRE(m);
}
}
TEST_CASE("Iterators") {
auto m = "CCCCCCC=N"_smiles;
REQUIRE(m);
SECTION("Atom Iterator") {
auto atoms = m->atoms();
auto n_atom = std::find_if(atoms.begin(), atoms.end(), [](const auto &a) {
return a->getAtomicNum() == 7;
});
REQUIRE(n_atom != atoms.end());
CHECK((*n_atom)->getIdx() == 7);
}
SECTION("Atom Neighbor Iterator") {
auto nbrs = m->atomNeighbors(m->getAtomWithIdx(6));
auto n_atom = std::find_if(nbrs.begin(), nbrs.end(), [](const auto &a) {
return a->getAtomicNum() == 7;
});
REQUIRE(n_atom != nbrs.end());
CHECK((*n_atom)->getIdx() == 7);
}
SECTION("Bond Iterator") {
auto bonds = m->bonds();
auto dbl_bnd = std::find_if(bonds.begin(), bonds.end(), [](const auto &b) {
return b->getBondType() == Bond::DOUBLE;
});
REQUIRE(dbl_bnd != bonds.end());
CHECK((*dbl_bnd)->getIdx() == 6);
}
SECTION("Atom Bond Iterator") {
auto nbr_bonds = m->atomBonds(m->getAtomWithIdx(6));
auto dbl_bnd = std::find_if(
nbr_bonds.begin(), nbr_bonds.end(),
[](const auto &b) { return b->getBondType() == Bond::DOUBLE; });
REQUIRE(dbl_bnd != nbr_bonds.end());
CHECK((*dbl_bnd)->getIdx() == 6);
}
}
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