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rdkit/External/ChemDraw/test.cpp
Greg Landrum 6b30df1e40 run clang-tidy and clang-format on the chemdraw files (#8837) 
* git tidy

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2025-10-03 11:21:56 -04:00

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//
// Copyright (c) 2024 Glysade Inc and other RDkit contributors
// All rights reserved.
//
// Redistribution and use in source and binary forms, with or without
// modification, are permitted provided that the following conditions are
// met:
//
// * Redistributions of source code must retain the above copyright
// notice, this list of conditions and the following disclaimer.
// * Redistributions in binary form must reproduce the above
// copyright notice, this list of conditions and the following
// disclaimer in the documentation and/or other materials provided
// with the distribution.
// * Neither the name of Novartis Institutes for BioMedical Research Inc.
// nor the names of its contributors may be used to endorse or promote
// products derived from this software without specific prior written
// permission.
//
// THIS SOFTWARE IS PROVIDED BY THE COPYRIGHT HOLDERS AND CONTRIBUTORS
// "AS IS" AND ANY EXPRESS OR IMPLIED WARRANTIES, INCLUDING, BUT NOT
// LIMITED TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR
// A PARTICULAR PURPOSE ARE DISCLAIMED. IN NO EVENT SHALL THE COPYRIGHT
// OWNER OR CONTRIBUTORS BE LIABLE FOR ANY DIRECT, INDIRECT, INCIDENTAL,
// SPECIAL, EXEMPLARY, OR CONSEQUENTIAL DAMAGES (INCLUDING, BUT NOT
// LIMITED TO, PROCUREMENT OF SUBSTITUTE GOODS OR SERVICES; LOSS OF USE,
// DATA, OR PROFITS; OR BUSINESS INTERRUPTION) HOWEVER CAUSED AND ON ANY
// THEORY OF LIABILITY, WHETHER IN CONTRACT, STRICT LIABILITY, OR TORT
// (INCLUDING NEGLIGENCE OR OTHERWISE) ARISING IN ANY WAY OUT OF THE USE
// OF THIS SOFTWARE, EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE.
//
#include "chemdraw.h"
#include <catch2/catch_all.hpp>
#include "RDGeneral/test.h"
#include <RDGeneral/Invariant.h>
#include <GraphMol/RDKitBase.h>
#include <GraphMol/FileParsers/FileParsers.h>
#include <GraphMol/SmilesParse/SmilesWrite.h>
#include <GraphMol/SmilesParse/SmilesParse.h>
#include <GraphMol/SmilesParse/SmartsWrite.h>
#include <RDGeneral/FileParseException.h>
#include <boost/algorithm/string.hpp>
#include <RDGeneral/BadFileException.h>
#include <GraphMol/SmilesParse/CanonicalizeStereoGroups.h>
#include <filesystem>
using namespace RDKit;
using namespace RDKit::v2;
std::string canon(const std::string &smi) {
auto *m = SmilesToMol(smi);
auto res = MolToSmiles(*m);
delete m;
return res;
}
void check_smiles_and_roundtrip(const RWMol &m, const std::string &expected) {
CHECK(MolToSmiles(m) == expected);
// std::cout << "*********" << std::endl;
// std::cout << MolToMolBlock(m) << std::endl;
std::unique_ptr<RWMol> mol(MolBlockToMol(MolToMolBlock(m)));
CHECK(MolToSmiles(*mol) == expected);
}
TEST_CASE("CDXML") {
std::string cdxmlbase =
std::string(getenv("RDBASE")) + "/Code/GraphMol/test_data/CDXML/";
SECTION("SIMPLE") {
std::string cdxml1 = R"(<?xml version="1.0" encoding="UTF-8" ?>
<!DOCTYPE CDXML SYSTEM "http://www.cambridgesoft.com/xml/cdxml.dtd" >
<CDXML
CreationProgram="ChemDraw JS 2.0.0.9"
Name="ACS Document 1996"
BoundingBox="94.75 178.16 154.89 211.17"
WindowPosition="0 0"
WindowSize="0 0"
FractionalWidths="yes"
InterpretChemically="yes"
ShowAtomQuery="yes"
ShowAtomStereo="no"
ShowAtomEnhancedStereo="yes"
ShowAtomNumber="no"
ShowResidueID="no"
ShowBondQuery="yes"
ShowBondRxn="yes"
ShowBondStereo="no"
ShowTerminalCarbonLabels="no"
ShowNonTerminalCarbonLabels="no"
HideImplicitHydrogens="no"
Magnification="666"
LabelFont="24"
LabelSize="10"
LabelFace="96"
CaptionFont="24"
CaptionSize="10"
HashSpacing="2.50"
MarginWidth="1.60"
LineWidth="0.60"
BoldWidth="2"
BondLength="14.40"
BondSpacing="18"
ChainAngle="120"
LabelJustification="Auto"
CaptionJustification="Left"
AminoAcidTermini="HOH"
ShowSequenceTermini="yes"
ShowSequenceBonds="yes"
ShowSequenceUnlinkedBranches="no"
ResidueWrapCount="40"
ResidueBlockCount="10"
ResidueZigZag="yes"
NumberResidueBlocks="no"
PrintMargins="36 36 36 36"
MacPrintInfo="0003000001200120000000000B6608A0FF84FF880BE309180367052703FC0002000001200120000000000B6608A0000100000064000000010001010100000001270F000100010000000000000000000000000002001901900000000000400000000000000000000100000000000000000000000000000000"
ChemPropName=""
ChemPropFormula="Chemical Formula: "
ChemPropExactMass="Exact Mass: "
ChemPropMolWt="Molecular Weight: "
ChemPropMOverZ="m/z: "
ChemPropAnalysis="Elemental Analysis: "
ChemPropBoilingPt="Boiling Point: "
ChemPropMeltingPt="Melting Point: "
ChemPropCritTemp="Critical Temp: "
ChemPropCritPres="Critical Pres: "
ChemPropCritVol="Critical Vol: "
ChemPropGibbs="Gibbs Energy: "
ChemPropLogP="Log P: "
ChemPropMR="MR: "
ChemPropHenry="Henry&apos;s Law: "
ChemPropEForm="Heat of Form: "
ChemProptPSA="tPSA: "
ChemPropID=""
ChemPropFragmentLabel=""
color="0"
bgcolor="1"
RxnAutonumberStart="1"
RxnAutonumberConditions="no"
RxnAutonumberStyle="Roman"
><colortable>
<color r="1" g="1" b="1"/>
<color r="0" g="0" b="0"/>
<color r="1" g="0" b="0"/>
<color r="1" g="1" b="0"/>
<color r="0" g="1" b="0"/>
<color r="0" g="1" b="1"/>
<color r="0" g="0" b="1"/>
<color r="1" g="0" b="1"/>
</colortable><fonttable>
<font id="24" charset="utf-8" name="Arial"/>
</fonttable><page
id="32"
BoundingBox="0 0 542 354"
Width="542"
Height="354"
HeaderPosition="36"
FooterPosition="36"
PageOverlap="0"
PrintTrimMarks="yes"
HeightPages="1"
WidthPages="1"
DrawingSpace="poster"
><fragment
id="10"
BoundingBox="94.75 178.16 154.89 211.17"
Z="4"
><n
id="7"
p="95.05 187.47"
Z="1"
AS="N"
/><n
id="9"
p="95.05 201.87"
Z="3"
AS="N"
/><n
id="11"
p="106.31 210.84"
Z="5"
AS="N"
/><n
id="13"
p="120.35 207.64"
Z="7"
AS="N"
/><n
id="15"
p="126.59 194.67"
Z="9"
AS="N"
/><n
id="17"
p="120.35 181.69"
Z="11"
AS="N"
/><n
id="19"
p="106.31 178.49"
Z="13"
AS="N"
/><n
id="28"
p="140.99 194.67"
Z="22"
NodeType="Nickname"
NeedsClean="yes"
AS="N"
><fragment
id="33"
><n
id="34"
p="148.17 207.09"
Element="8"
NumHydrogens="0"
/><n
id="35"
p="162.52 207.09"
/><n
id="36"
p="176.87 207.09"
/><n
id="37"
p="169.69 194.67"
/><n
id="38"
p="169.69 219.52"
/><n
id="39"
p="140.99 194.67"
/><n
id="40"
p="148.17 182.24"
Element="8"
NumHydrogens="0"
/><n
id="41"
p="126.64 194.67"
NodeType="ExternalConnectionPoint"
/><b
id="42"
B="39"
E="40"
Order="2"
/><b
id="43"
B="35"
E="38"
/><b
id="44"
B="35"
E="36"
/><b
id="45"
B="35"
E="37"
/><b
id="46"
B="34"
E="35"
/><b
id="47"
B="34"
E="39"
/><b
id="48"
B="41"
E="39"
/></fragment><t
p="137.66 198.28"
BoundingBox="137.66 189.64 154.89 198.28"
LabelJustification="Left"
LabelAlignment="Left"
><s font="24" size="9.95" color="0" face="96">Boc</s></t></n><b
id="21"
Z="15"
B="7"
E="9"
BS="N"
/><b
id="22"
Z="16"
B="9"
E="11"
BS="N"
/><b
id="23"
Z="17"
B="11"
E="13"
BS="N"
/><b
id="24"
Z="18"
B="13"
E="15"
BS="N"
/><b
id="25"
Z="19"
B="15"
E="17"
BS="N"
/><b
id="26"
Z="20"
B="17"
E="19"
BS="N"
/><b
id="27"
Z="21"
B="19"
E="7"
BS="N"
/><b
id="29"
Z="23"
B="15"
E="28"
BS="N"
/></fragment></page></CDXML>)";
std::stringstream iss(cdxml1);
{
auto mols = MolsFromChemDrawDataStream(iss);
for (auto &mol : mols) {
CHECK(MolToSmiles(*mol) == "CC(C)(C)OC(=O)C1CCCCCC1");
}
}
}
}
TEST_CASE("CDXML Advanced") {
std::string cdxmlbase =
std::string(getenv("RDBASE")) + "/Code/GraphMol/test_data/CDXML/";
SECTION("RING CHIRALITY") {
std::string fname = cdxmlbase + "ring-stereo1.cdxml";
std::vector<std::string> expected = {"C1CC[C@H]2CCCC[C@H]2C1"};
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
SECTION("SIMPLE CHIRAL") {
std::string fname = cdxmlbase + "chirality1.cdxml";
std::vector<std::string> expected = {"C[C@H](N)C[C@H](C)N"};
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
SECTION("CDXML-CISTRANS") {
auto fname = cdxmlbase + "cistrans1.cdxml";
std::vector<std::string> expected = {"F/C(I)=C(\\Cl)Br"};
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
SECTION("DEUTERIUM") {
auto fname = cdxmlbase + "deuterium.cdxml";
{
std::vector<std::string> expected = {
"[2H]c1c([2H])c([2H])c([2H])c([2H])c1[2H]"};
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
{
std::vector<std::string> expected = {
"[2H]C1=C([2H])C([2H])=C([2H])C([2H])=C1[2H]"};
ChemDrawParserParams params;
params.sanitize = false;
params.removeHs = false;
auto mols = MolsFromChemDrawFile(fname, params);
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
{
std::vector<std::string> expected = {
"[2H]C1=C([2H])C([2H])=C([2H])C([2H])=C1[2H]"};
ChemDrawParserParams params;
params.sanitize = false;
params.removeHs = true;
auto mols = MolsFromChemDrawFile(fname, params);
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
}
SECTION("Queries") {
{
auto fname = cdxmlbase + "query-atoms.cdxml";
std::vector<std::string> expected = {"*c1ccccc1", "*c1ccccc1",
"*c1ccccc1"};
std::vector<std::string> expected_smarts = {
"[#6]1:[#6]:[#6]:[#6]:[#6]:[#6]:1-*",
"[#6]1:[#6]:[#6]:[#6]:[#6]:[#6]:1-[!#1]",
"[#6]1:[#6]:[#6]:[#6]:[#6]:[#6]:1-[!#6&!#1]"};
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
CHECK(MolToSmarts(*mol) == expected_smarts[i]);
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
{
auto fname = cdxmlbase + "anybond.cdxml";
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == 1);
CHECK(MolToSmiles(*mols[0]) == "C1CCC~CC1");
CHECK(MolToSmarts(*mols[0]) == "[#6]1~[#6]-[#6]-[#6]-[#6]-[#6]-1");
}
}
SECTION("ElementList") {
auto fname = cdxmlbase + "element-list.cdxml";
std::vector<std::string> expected = {"[C]CC"};
std::vector<std::string> expected_smarts = {"[#6]-[#6]-[#6,#7,#8,#16]"};
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
CHECK(MolToSmarts(*mol) == expected_smarts[i]);
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
SECTION("Enhanced Stereo") {
auto fname = cdxmlbase + "beta-cypermethrin.cdxml";
std::vector<std::string> expected = {
"CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@@H](C#N)c1cccc(Oc2ccccc2)c1"};
std::vector<std::string> expected_cx = {
"CC1(C)[C@H](C=C(Cl)Cl)[C@@H]1C(=O)O[C@H](C#N)c1cccc(Oc2ccccc2)c1 |&1:3,&2:8,12|"};
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
mol.get()->clearConformers();
CHECK(MolToSmiles(*mol) == expected[i]);
CHECK(MolToCXSmiles(*mol) == expected_cx[i++]);
}
}
SECTION("Enhanced Stereo 2") {
auto fname = cdxmlbase + "beta-cypermethrin-or-abs.cdxml";
std::vector<std::string> expected = {
"CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@@H](C#N)c1cccc(Oc2ccccc2)c1"};
std::vector<std::string> expected_cx = {
"CC1(C)[C@H](C=C(Cl)Cl)[C@@H]1C(=O)O[C@H](C#N)c1cccc(Oc2ccccc2)c1 |a:3,o1:8,12|"};
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == expected.size());
int i = 0;
SmilesWriteParams wp;
for (auto &mol : mols) {
auto tomol = std::unique_ptr<ROMol>((ROMol *)mol.release());
tomol.get()->clearConformers();
RDKit::canonicalizeStereoGroups(tomol);
CHECK(MolToSmiles(*tomol) == expected[i]);
CHECK(MolToCXSmiles(*tomol, wp) == expected_cx[i++]);
}
}
SECTION("Bad CDXML") {
auto fname = cdxmlbase + "bad-cdxml.cdxml";
// Only one passes sanitization
{
std::vector<std::string> expected = {"*c1ccccc1"};
std::vector<std::string> expected_smarts = {
"[#6]1:[#6]:[#6]:[#6]:[#6]:[#6]:1-*",
};
auto params = ChemDrawParserParams();
auto mols = MolsFromChemDrawFile(fname, params);
for (auto &mol : mols) {
std::cerr << MolToSmarts(*mol) << std::endl;
std::cerr << MolToSmiles(*mol) << std::endl;
}
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
CHECK(MolToSmarts(*mol) == expected_smarts[i]);
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
// setting sanitization to false, we get both
std::vector<std::string> expected = {"*C1=C([H])C([H])=C([H])C([H])=C1[H]",
"*C1=C([H])N([H])=C([H])C([H])=C1[H]"};
std::vector<std::string> expected_smarts = {
"[#6]1(=[#6](-[#6](=[#6](-[#6](=[#6]-1-*)-[H])-[H])-[H])-[H])-[H]",
"[#6]1(=[#6](-[#6](=[#7](-[#6](=[#6]-1-[!#1])-[H])-[H])-[H])-[H])-[H]",
};
ChemDrawParserParams params;
params.sanitize = false;
auto mols = MolsFromChemDrawFile(fname, params);
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
CHECK(MolToSmarts(*mol) == expected_smarts[i]);
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
SECTION("Fusion with chirality") {
auto fname = cdxmlbase + "fusion-chiral.cdxml";
auto mols = MolsFromChemDrawFile(fname);
std::vector<std::string> expected = {"C[C@@H](O)[C@@H](C)O"};
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
SECTION("deuterium atom") {
auto fname = cdxmlbase + "deuterium-atom.cdxml";
ChemDrawParserParams params;
params.sanitize = false;
params.removeHs = false;
auto mols = MolsFromChemDrawFile(fname, params);
std::vector<std::string> expected = {"[2H]"};
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
SECTION("ChemDraw Template 2 from the synthesis-workshop") {
// this was another hella fun to validate the stereo-chemistry...
// there were so many stereo warnings in chemdraw, I'm just going to
// assume the rdkit is correct here...
auto fname = cdxmlbase + "chemdraw_template2.cdxml";
std::string talatisamine =
"CCN1C[C@]2(COC)CCC(OC)[C@@]34[C@@H]5C[C@@H]6C(OC)C[C@@](O)([C@H]5[C@H]6O)[C@@H](C[C@H]23)[C@H]14";
auto mols = MolsFromChemDrawFile(fname);
std::vector<std::string> expected = {
talatisamine, // 0
"*",
"C",
"[F]",
"[B]",
"[C]",
"[2H]",
talatisamine,
"*",
"C",
"[F]", // 10
"[B]",
"[C]",
"[2H]",
talatisamine,
"*",
"C",
"[F]",
"[B]",
"[C]",
"[2H]", // 20
talatisamine,
"*",
"C",
"[F]",
"[B]",
"[C]",
"[2H]",
talatisamine,
"CCN1C[C@]2(COC)CC[C@H](OC)[C@]34C1C(C[C@H]23)[C@@]1(O)CC(OC)[C@H]2C[C@@H]4[C@@H]1[C@H]2O",
"*", // 30
"[B]",
"[C]",
"[2H]",
"C",
"[F]",
"*",
"C",
"[F]",
"[B]",
"[C]", // 40
"[2H]",
talatisamine,
"*",
"C",
"[F]",
"[B]",
"[C]",
"[2H]",
talatisamine,
"*", // 50
"C",
"[F]",
"[B]",
"[C]",
"[2H]",
"CC1CC[C@]2(O)[C@]3(C)C[C@]4(O)O[C@@]2([C@@H]1O)C1(O)C4(C)C(O)(C(C)C)[C@@H](O)[C@]13O",
"CC1=C(C(C)C)[C@@H](O)[C@@]2(O)[C@@]3(C)CC(=O)O[C@@]4([C@H](O)C(C)CC[C@]34O)[C@@]12O",
"CC1=C[C@@]23OC(=O)C[C@@](C)([C@@]2(O)CC1)[C@]1(O)[C@H](O)C2(C(C)C)OC2(C)[C@@]31O",
"*",
"[B]", // 60
"[C]",
"CC1CC[C@@H]2[C@]3(C)C[C@@H]4O[C@@]2(C1)C1[C@@H]3CC(C(C)C)C14C",
"[2H]",
"*",
"[B]",
"[C]",
"C",
"CC1CC[C@]2(O)[C@]3(C)C[C@]4(O)O[C@@]2([C@@H]1O)C1(O)C4(C)C(O)(C(C)C)[C@@H](O)[C@]13O",
"[2H]"};
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
INFO(std::to_string(i) + " " + MolToSmiles(*mol));
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
SECTION("ChemDraw Template 3 from the synthesis-workshop") {
// this was another hella fun to validate the stereo-chemistry...
// there were so many stereo warnings in chemdraw, I'm just going to
// assume
// the rdkit is correct here...
auto fname = cdxmlbase + "chemdraw_template3.cdxml";
auto mols = MolsFromChemDrawFile(fname);
std::vector<std::string> expected = {
"CCC/C=C/C=C/C(=O)O[C@H]1/C(=C/C(=O)OC)C[C@H]2C[C@H]([C@@H](C)O)OC(=O)C[C@H](O)C[C@@H]3C[C@H](OC(C)=O)C(C)(C)[C@](O)(C[C@@H]4C/C(=C/C(=O)OC)C[C@H](/C=C/C(C)(C)[C@]1(O)O2)O4)O3",
"[B]",
"*",
"[C]",
"CCC/C=C/C=C/C(=O)O[C@H]1/C(=C/C(=O)OC)C[C@H]2C[C@H]([C@@H](C)O)OC(=O)C[C@H](O)C[C@@H]3C[C@H](OC(C)=O)C(C)(C)[C@](O)(C[C@@H]4C/C(=C/C(=O)OC)C[C@H](/C=C/C(C)(C)[C@]1(O)O2)O4)O3",
"[B]",
"*",
"[C]",
"CCC/C=C/C=C/C(=O)O[C@H]1/C(=C/C(=O)OC)C[C@@H](C[C@@H](O)[C@@H](C)O)O[C@@]1(O)C(C)(C)/C=C/C=O",
"*",
"[C]",
"C=C(C[C@H]([O])C[C@]1(O)O[C@H](C[C@@H](O)CC(=O)O)C[C@H](OC(C)=O)C1(C)C)C[Si](C)(C)C",
"*.CC[Si](CC)CC",
"CC[Si](C)(CC)CC",
"CC[Si](C)(CC)CC",
"CC",
"CC",
"*",
"C=C(C[C@H]([O])C[C@]1(O)O[C@H](C[C@@H](O)CC(=O)O)C[C@H](OC(C)=O)C1(C)C)C[Si](C)(C)C",
"*.CC[Si](CC)CC",
"CCC/C=C/C=C/C(=O)O[C@H]1/C(=C/C(=O)OC)C[C@@H](C[C@@H](O)[C@@H](C)O)O[C@@]1(O)C(C)(C)/C=C/C=O",
"[C]"};
int i = 0;
for (auto &mol : mols) {
INFO(i);
check_smiles_and_roundtrip(*mol, expected[i++]);
}
}
SECTION("protecting group") {
auto fname = cdxmlbase + "protecting-groups.cdxml";
auto mols = MolsFromChemDrawFile(fname);
std::vector<std::string> expected = {"CC[Si](C)(CC)CC", "CC"};
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
check_smiles_and_roundtrip(*mol, expected[i++]);
}
}
SECTION("protecting group 2") {
auto fname = cdxmlbase + "protecting-groups2.cdxml";
auto mols = MolsFromChemDrawFile(fname);
std::vector<std::string> expected = {"CC[Si](C)(CC)CC", "CC"};
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
check_smiles_and_roundtrip(*mol, expected[i++]);
}
}
SECTION("floating protecting group") {
auto fname = cdxmlbase + "floating-protecting-group.cdxml";
// This is a weird one, chemdraw simply ignores the error that causes the
// bond issue, we should probably drop the floating fragment here if
// we are sanitizing
auto mols = MolsFromChemDrawFile(fname);
std::vector<std::string> expected = {
"*",
"C=C(C[C@H]([O])C[C@]1(O)O[C@H](C[C@@H](O)CC(=O)O)C[C@H](OC(C)=O)C1(C)C)C[Si](C)(C)C",
"*.CC[Si](CC)CC"};
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
INFO(i);
check_smiles_and_roundtrip(*mol, expected[i++]);
}
}
SECTION("Missing File Name") {
try {
auto mols = MolsFromChemDrawFile("missing file");
CHECK(0); // Bad file exception not caught
} catch (RDKit::BadFileException &) {
}
}
SECTION("Aromatic ring (bondorder==4") {
auto fname = cdxmlbase + "aromatic.cdxml";
auto mols = MolsFromChemDrawFile(fname);
std::vector<std::string> expected = {"c1ccccc1"};
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
check_smiles_and_roundtrip(*mol, expected[i++]);
}
}
SECTION("Malformed") {
auto fname = cdxmlbase + "malformed.cdxml";
try {
auto mols = MolsFromChemDrawFile(fname);
CHECK(0);
} catch (FileParseException &e) {
// CHECK(std::string(e.what()) == "expected > at line: 373");
}
}
SECTION("Lots of stereo") {
{
auto fname = cdxmlbase + "stereo.cdxml";
std::vector<std::string> expected = {
"C[C@@H](Cl)[C@H](N)O.C[C@@H](F)[C@H](N)O.C[C@H](Br)[C@@H](N)O.C[C@H](I)[C@@H](N)O"};
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
check_smiles_and_roundtrip(*mol, expected[i++]);
}
}
{ // The above, but broken out for easier testing
std::vector<std::string> filenames = {"stereo1.cdxml", "stereo2.cdxml",
"stereo3.cdxml", "stereo4.cdxml"};
std::vector<std::string> expected = {
"C[C@H](I)[C@@H](N)O", "C[C@@H](I)[C@H](N)O", "C[C@@H](Cl)[C@H](N)O",
"C[C@H](Br)[C@@H](N)O"};
for (auto i = 0u; i < filenames.size(); ++i) {
auto fname = cdxmlbase + filenames[i];
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == 1);
auto &m = *mols.back();
check_smiles_and_roundtrip(m, expected[i]);
}
}
{
auto fname = cdxmlbase + "wavy.cdxml";
std::vector<std::string> expected = {"Cc1cccc(C)c1NC(=O)N=C1CCCN1C",
"Cc1cccc(C)c1NC(=O)/N=C1\\CCCN1C"};
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
if (i == 0) {
CHECK(mol->getBondWithIdx(11)->getStereo() ==
Bond::BondStereo::STEREOANY);
}
check_smiles_and_roundtrip(*mol, expected[i++]);
}
}
{
auto fname = cdxmlbase + "wavy-single.cdxml";
std::vector<std::string> expected = {"CCCC"};
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
CHECK(mol->getBondWithIdx(0)->getBondDir() == Bond::BondDir::NONE);
CHECK(mol->getBondWithIdx(1)->getBondDir() == Bond::BondDir::NONE);
CHECK(mol->getBondWithIdx(2)->getBondDir() == Bond::BondDir::NONE);
check_smiles_and_roundtrip(*mol, expected[i++]);
}
}
}
SECTION("Lots of bad stereo") {
{
auto fname = cdxmlbase + "bad-id.cdxml";
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == 0);
}
{
auto fname = cdxmlbase + "bad-coords.cdxml";
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == 0);
}
{
auto fname = cdxmlbase + "bad-bondorder2.cdxml";
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == 0);
}
}
}
TEST_CASE("REACTIONS") {
std::string cdxmlbase =
std::string(getenv("RDBASE")) + "/Code/GraphMol/test_data/CDXML/";
SECTION("REACTION") {
std::string fname = cdxmlbase + "reaction-with-boc.cdxml";
std::vector<std::string> expected = {"CC(C)(C)OC(=O)C1CCCCCC1[*:1]",
"c1ccc([*:1])cc1", "C1CC1", "C1CCC1"};
{
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
{
// v1 api
auto mols = MolsFromChemDrawFile(fname);
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
}
SECTION("REACTION2") {
auto fname = cdxmlbase + "rxn1.cdxml";
std::vector<std::string> expected = {
"Cl[c:1]1[cH:4][cH:3][cH:2][cH:6][cH:5]1",
"OC(O)B[c:7]1[cH:8][cH:9][cH:10][cH:11][cH:12]1",
"[cH:1]1[cH:4][cH:3][cH:2][c:6](-[c:7]2[cH:8][cH:9][cH:10][cH:11][cH:12]2)[cH:5]1"};
auto mols = MolsFromChemDrawFile(fname);
int i = 0;
for (auto &mol : mols) {
CHECK(mol->getProp<unsigned int>("CDX_SCHEME_ID") == 397);
CHECK(mol->getProp<unsigned int>("CDX_STEP_ID") == 398);
if (i == 0) {
CHECK(mol->getProp<unsigned int>("CDX_REAGENT_ID") == 0);
} else if (i == 1) {
CHECK(mol->getProp<unsigned int>("CDX_REAGENT_ID") == 1);
} else if (i == 2) {
CHECK(mol->getProp<unsigned int>("CDX_PRODUCT_ID") == 0);
}
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
}
TEST_CASE("atropisomers") {
std::string cdxmlbase =
std::string(getenv("RDBASE")) + "/Code/GraphMol/test_data/CDXML/";
SECTION("atropisomer") {
{
// XXX the rounding here is a little different from the original RDKit
// CDXML parser 0.64->0.39999
// This is something we should probably figure out.
std::vector<std::string> filenames = {"atrop1.cdxml"};
std::vector<std::string> expected = {
"C[C]1[C][CH]C(Cl)C(C)=C1c1c(C)ccc(Cl)c1C |(-2.936,-0.12,;-2.936,-1.66,;-1.602,-2.43,;-1.602,-3.97,;-2.936,-4.74,;-2.93,-6.28,;-4.27,-3.97,;-5.603,-4.74,;-4.27,-2.43,;-5.603,-1.66,;-5.603,-0.12,;-4.27,0.639999,;-6.937,0.639999,;-8.271,-0.12,;-8.271,-1.66,;-9.604,-2.43,;-6.937,-2.43,;-6.937,-3.97,),^1:1,3,^2:2,wU:8.8|"};
for (auto i = 0u; i < filenames.size(); ++i) {
auto fname = cdxmlbase + filenames[i];
auto mol = MolsFromChemDrawFile(fname);
SmilesWriteParams ps;
auto smi = MolToCXSmiles(*(mol[0].get()), ps,
SmilesWrite::CXSmilesFields::CX_ALL);
CHECK(smi == expected[i]);
}
}
}
}
TEST_CASE("bad stereo in a natural product") {
std::string cdxmlbase =
std::string(getenv("RDBASE")) + "/Code/GraphMol/test_data/CDXML/";
SECTION("case 1") {
auto fname = cdxmlbase + "stereo5.cdxml";
auto mols = MolsFromChemDrawFile(fname);
REQUIRE(mols.size() == 1);
CHECK(
MolToSmiles(*mols[0]) ==
"Cc1ccc2n1[C@@H]1[C@@H]3O[C@]([C@H](C)O)(C=C2)[C@H]1c1ccc(C)n1[C@@H]3C");
}
}
TEST_CASE("Github #6262: preserve bond wedging") {
std::string cdxmlbase =
std::string(getenv("RDBASE")) + "/Code/GraphMol/test_data/CDXML/";
SECTION("case 1") {
auto fname = cdxmlbase + "stereo6.cdxml";
auto mols = MolsFromChemDrawFile(fname);
REQUIRE(mols.size() == 1);
{
REQUIRE(mols[0]->getBondBetweenAtoms(2, 5));
unsigned int cfg = 0;
CHECK(mols[0]->getBondBetweenAtoms(2, 5)->getPropIfPresent(
common_properties::_MolFileBondCfg, cfg));
CHECK(cfg == 1);
}
{
REQUIRE(mols[0]->getBondBetweenAtoms(1, 4));
unsigned int cfg = 0;
CHECK(mols[0]->getBondBetweenAtoms(1, 4)->getPropIfPresent(
common_properties::_MolFileBondCfg, cfg));
CHECK(cfg == 3);
}
{
REQUIRE(mols[0]->getBondBetweenAtoms(3, 8));
unsigned int cfg = 0;
CHECK(mols[0]->getBondBetweenAtoms(3, 8)->getPropIfPresent(
common_properties::_MolFileBondCfg, cfg));
CHECK(cfg == 2);
}
}
}
TEST_CASE("Github #6887: and1 or1 in same mol") {
SECTION("case 1") {
std::string cdxml1 = R"(<?xml version="1.0" encoding="UTF-8" ?>
<!DOCTYPE CDXML SYSTEM "http://www.cambridgesoft.com/xml/cdxml.dtd" >
<CDXML
CreationProgram="ChemDraw 21.0.0.28"
Name="Untitled A4 Document-2"
BoundingBox="115.75 357.32 272.13 406.58"
WindowPosition="0 0"
WindowSize="0 0"
FractionalWidths="yes"
InterpretChemically="yes"
ShowAtomQuery="yes"
ShowAtomStereo="no"
ShowAtomEnhancedStereo="yes"
ShowAtomNumber="no"
ShowResidueID="no"
ShowBondQuery="yes"
ShowBondRxn="yes"
ShowBondStereo="no"
ShowTerminalCarbonLabels="no"
ShowNonTerminalCarbonLabels="no"
HideImplicitHydrogens="no"
LabelFont="21"
LabelSize="10"
LabelFace="96"
CaptionFont="510"
CaptionSize="12"
HashSpacing="2.70"
MarginWidth="2"
LineWidth="1"
BoldWidth="4"
BondLength="30"
BondSpacing="12"
ChainAngle="120"
LabelJustification="Auto"
CaptionJustification="Left"
AminoAcidTermini="HOH"
ShowSequenceTermini="yes"
ShowSequenceBonds="yes"
ShowSequenceUnlinkedBranches="no"
ResidueWrapCount="40"
ResidueBlockCount="10"
ResidueZigZag="yes"
NumberResidueBlocks="no"
PrintMargins="36 36 36 36"
color="0"
bgcolor="1"
><colortable>
<color r="1" g="1" b="1"/>
<color r="0" g="0" b="0"/>
<color r="1" g="0" b="0"/>
<color r="1" g="1" b="0"/>
<color r="0" g="1" b="0"/>
<color r="0" g="1" b="1"/>
<color r="0" g="0" b="1"/>
<color r="1" g="0" b="1"/>
</colortable><fonttable>
<font id="21" charset="x-mac-roman" name="Helvetica"/>
<font id="510" charset="x-mac-roman" name="Times New Roman"/>
</fonttable><page
id="24"
BoundingBox="0 0 523 770"
HeaderPosition="36"
FooterPosition="36"
PrintTrimMarks="yes"
HeightPages="1"
WidthPages="1"
><fragment
id="3"
BoundingBox="115.75 357.32 272.13 406.58"
Z="2"
><n
id="2"
p="116 406"
Z="1"
AS="N"
/><n
id="4"
p="141.98 391"
Z="3"
Geometry="Tetrahedral"
AS="N"
BondOrdering="5 7 0 17"
EnhancedStereoType="And"
EnhancedStereoGroupNum="1"
><objecttag
TagType="Unknown"
Name="enhancedstereo"
><t
p="137.96 401.37"
BoundingBox="138.29 396 145.62 401.50"
CaptionLineHeight="variable"
><s font="21" size="7.5" color="0">&amp;1</s></t></objecttag></n><n
id="6"
p="167.96 406"
Z="5"
AS="N"
/><n
id="8"
p="193.94 391"
Z="7"
Geometry="Tetrahedral"
AS="N"
BondOrdering="9 11 0 19"
EnhancedStereoType="Or"
EnhancedStereoGroupNum="2"
><objecttag
TagType="Unknown"
Name="enhancedstereo"
><t
p="188.54 401.26"
BoundingBox="188.76 396 199.07 401.41"
CaptionLineHeight="variable"
><s font="21" size="7.5" color="0">or2</s></t></objecttag></n><n
id="10"
p="219.92 406"
Z="9"
AS="N"
/><n
id="12"
p="245.90 391"
Z="11"
Geometry="Tetrahedral"
AS="N"
BondOrdering="13 15 0 21"
EnhancedStereoType="Or"
EnhancedStereoGroupNum="1"
><objecttag
TagType="Unknown"
Name="enhancedstereo"
><t
p="241.11 401.22"
BoundingBox="241.32 396 250.43 401.36"
CaptionLineHeight="variable"
><s font="21" size="7.5" color="0">or1</s></t></objecttag></n><n
id="14"
p="271.88 406"
Z="13"
AS="N"
/><n
id="16"
p="141.98 361"
Z="15"
NodeType="Fragment"
NeedsClean="yes"
AS="N"
><fragment
id="25"
><n
id="26"
p="141.98 361"
Element="8"
NumHydrogens="0"
/><n
id="27"
p="116 346"
NumHydrogens="3"
/><n
id="28"
p="141.98 391"
NodeType="ExternalConnectionPoint"
/><b
id="29"
B="26"
E="27"
/><b
id="30"
B="28"
E="26"
Display="WedgeBegin"
/></fragment><t
p="138.09 364.68"
BoundingBox="138.48 357.32 159.33 364.89"
LabelJustification="Left"
LabelAlignment="Left"
><s font="21" size="10" color="0" face="96">OMe</s></t></n><n
id="18"
p="193.94 361"
Z="17"
Element="17"
NumHydrogens="0"
NeedsClean="yes"
AS="N"
><t
p="190.33 364.68"
BoundingBox="190.77 357.32 199.10 364.87"
LabelJustification="Left"
LabelAlignment="Left"
><s font="21" size="10" color="0" face="96">Cl</s></t></n><n
id="20"
p="245.90 361"
Z="19"
Element="35"
NumHydrogens="0"
NeedsClean="yes"
AS="N"
><t
p="242.57 364.59"
BoundingBox="243.31 357.41 252.45 364.59"
LabelJustification="Left"
LabelAlignment="Left"
><s font="21" size="10" color="0" face="96">Br</s></t></n><b
id="5"
Z="4"
B="2"
E="4"
BS="N"
/><b
id="7"
Z="6"
B="4"
E="6"
BS="N"
/><b
id="9"
Z="8"
B="6"
E="8"
BS="N"
/><b
id="11"
Z="10"
B="8"
E="10"
BS="N"
/><b
id="13"
Z="12"
B="10"
E="12"
BS="N"
/><b
id="15"
Z="14"
B="12"
E="14"
BS="N"
/><b
id="17"
Z="16"
B="4"
E="16"
Display="WedgeBegin"
BS="N"/><b
id="19"
Z="18"
B="8"
E="18"
Display="WedgeBegin"
BS="N"
/><b
id="21"
Z="20"
B="12"
E="20"
Display="WedgeBegin"
BS="N"
/></fragment></page></CDXML>
)";
std::stringstream iss(cdxml1);
auto mols = MolsFromChemDrawDataStream(iss);
mols[0]->clearConformers();
CHECK(MolToCXSmiles(*mols[0]) ==
"CO[C@H](C)C[C@H](Cl)C[C@H](C)Br |o1:5,o2:8,&1:2|");
}
}
TEST_CASE("Github #7528 - read fragments in groups") {
std::string cdxmlbase =
std::string(getenv("RDBASE")) + "/Code/GraphMol/test_data/CDXML/";
SECTION("case 1") {
auto fname = cdxmlbase + "github7467-grouped-fragments.cdxml";
ChemDrawParserParams params;
params.sanitize = false;
auto mols = MolsFromChemDrawFile(fname, params);
REQUIRE(mols.size() == 2);
}
}
TEST_CASE("Github #7501 - dative bonds") {
std::string cdxmlbase =
std::string(getenv("RDBASE")) + "/Code/GraphMol/test_data/CDXML/";
SECTION("case 1") {
auto fname = cdxmlbase + "github7501-dative.cdxml";
ChemDrawParserParams params;
auto mols = MolsFromChemDrawFile(fname, params);
CHECK(MolToSmiles(*mols[0]) ==
"C[CH2](C)->[Os]12<-[CH3]CC[NH]->1CC=[NH]->2"); // All datives to the
// Osmium
}
}
TEST_CASE("Synthesis-workshop") {
std::string cdxmlbase =
std::string(getenv("RDBASE")) + "/Code/GraphMol/test_data/CDXML/";
SECTION("ChemDraw Template from the synthesis-workshop") {
// this was hella fun to validate the stereo-chemistry...
auto fname = cdxmlbase + "chemdraw_template1.cdxml";
auto mols = MolsFromChemDrawFile(fname);
std::vector<std::string> expected = {
"CCC/C=C/C=C/C(=O)O[C@H]1/C(=C/C(=O)OC)C[C@H]2C[C@H]([C@@H](C)O)OC(=O)C[C@H](O)C[C@@H]3C[C@H](OC(C)=O)C(C)(C)[C@](O)(C[C@@H]4C/C(=C/C(=O)OC)C[C@H](/C=C/C(C)(C)[C@]1(O)O2)O4)O3",
"[B]", "*", "[C]",
"Cc1ccc2n1[C@@H]1[C@@H]3O[C@]([C@H](C)O)(C=C2)[C@H]1c1ccc(C)n1[C@@H]3C",
// this is may or may not be correct, but the structure is drawn
// incorrectly.
// There's a test below which fixes this
"Cc1ccc2n1[C@H](C)C(=O)[C@@H]1[C@H]2C(=O)C=Cc2ccc(C)n21",
"Cc1ccc2ccc(=O)ccn12", "Cc1cccn1[C@H](C)C=O",
"Cc1ccc2ccc([O-])cc[n+]1-2", "Cc1ccc2ccc(=O)ccn12",
"Cc1cccn1[C@H](C)C(C#N)O[Si](C)(C)C",
"CC1CC[C@]2(O)[C@]3(C)C[C@]4(O)O[C@@]2([C@@H]1O)C1(O)C4(C)C(O)(C(C)C)[C@@H](OC(=O)c2ccc[nH]2)[C@]13O",
"C=C(C)[C@H]1CC(=O)CC2=C(C1)[C@H]1C(=O)O[C@H]3C[C@@](C)(O)[C@@H](C2=O)[C@@H]13"};
CHECK(mols.size() == expected.size());
int i = 0;
for (auto &mol : mols) {
INFO(i);
CHECK(MolToSmiles(*mol) == expected[i++]);
}
}
}
TEST_CASE("Output CDXML") {
SECTION("basic") {
auto mol =
"N#Cc1ccc(cc1Cl)O[C@@H]1CC[C@H](CC1)NC(=O)c1ccc(nn1)N1CCC(CC1)CN1CCN(CC1)c1cc2C(=O)N(C(=O)c2cc1F)C1CCC(=O)NC1=O"_smiles;
// auto mol = "[C@H](I)(F)Br"_smiles;
// auto res = MolToMolBlock(*mol);
// mol->debugMol(std::cerr);
std::string output = MolToChemDrawBlock(*mol);
std::stringstream cdxml;
cdxml << output;
auto mols = MolsFromChemDrawDataStream(cdxml);
CHECK(MolToSmiles(*mols[0]) == MolToSmiles(*mol));
}
}
TEST_CASE("Brackets") {
std::string cdxmlbase =
std::string(getenv("RDBASE")) + "/Code/GraphMol/test_data/CDXML/";
SECTION("MultipleGroups") {
auto fname = cdxmlbase + "sgroups_and_remove_atoms_4.cdxml";
ChemDrawParserParams params;
auto mols = MolsFromChemDrawFile(fname, params);
CHECK(MolToSmiles(*mols[0]) == "CCN(C)CC");
}
}
TEST_CASE("Enhanced Stereochem") {
SECTION("Round Trip") {
auto mol = "F[C@H](Cl)Br |o1:1|"_smiles;
CHECK(MolToCXSmiles(*mol) == "F[C@H](Cl)Br |o1:1|");
auto cdx = MolToChemDrawBlock(*mol);
std::stringstream iss(cdx);
auto mols = MolsFromChemDrawDataStream(iss);
SmilesWriteParams ps;
auto cxsmi = MolToCXSmiles(*mols[0], ps,
SmilesWrite::CXSmilesFields::CX_ALL ^
SmilesWrite::CXSmilesFields::CX_COORDS);
CHECK(cxsmi == "F[C@H](Cl)Br |o1:1|");
}
}
TEST_CASE("Round TRIP") {
std::string path =
std::string(getenv("RDBASE")) + "/Code/GraphMol/test_data/";
std::string code_path = std::string(getenv("RDBASE"));
SECTION("round trip") {
std::set<std::string> exceptions = {"stereo3d_unknown.mol", "mrv-sma.mol",
"github2040_1.mol"};
int failed = 0;
int total = 0;
RDLog::LogStateSetter blocker;
for (const auto &entry :
std::filesystem::recursive_directory_iterator(code_path)) {
if (entry.path().string().find("ChemDraw") != std::string::npos) {
continue; // Skip ChemDraw directory
}
if (entry.path().string().find("build") != std::string::npos) {
continue;
}
if (entry.is_regular_file() &&
entry.path().extension().string() == ".mol") {
if (exceptions.find(entry.path().filename().string()) !=
exceptions.end()) {
std::cerr << "Skipping exception: " << entry.path() << std::endl;
continue;
}
RWMol *mol = nullptr;
try {
mol = MolFileToMol(entry.path().string());
} catch (...) {
continue;
}
if (mol) {
// CDX doesn't support atom map numbers apparently
total++;
for (auto atom : mol->atoms()) {
atom->setAtomMapNum(0);
}
// CDXML doesn't support ZERO bonds
bool haszerobond = false;
for (auto bond : mol->bonds()) {
if (bond->getBondType() == Bond::BondType::ZERO) {
haszerobond = true;
break;
}
}
if (haszerobond) {
delete mol;
continue;
}
// std::cerr << entry.path() << std::endl;
std::string cdx;
try {
cdx = MolToChemDrawBlock(*mol);
} catch (...) {
std::cerr << entry.path().filename().string() << std::endl;
std::cerr << "FAIL (cdxml-write-exception):" << entry.path()
<< std::endl;
failed++;
continue;
}
std::vector<std::unique_ptr<RWMol>> mols;
std::stringstream iss(cdx);
try {
mols = MolsFromChemDrawDataStream(iss);
} catch (...) {
std::cerr << entry.path().filename().string() << std::endl;
std::cerr << "FAIL (cdxml-exception):" << entry.path() << std::endl;
failed++;
}
auto smi1 = MolToSmiles(*mol);
if (mols.size() == 0) {
std::cerr << entry.path().filename().string() << std::endl;
std::cerr << "FAIL (nomol):" << entry.path() << std::endl;
mol->debugMol(std::cerr);
failed++;
continue;
}
auto smi2 = MolToSmiles(*mols[0]);
if (smi1 != smi2) {
// std::cerr <<
// "**************************************************************"
// << std::endl;
std::cerr << "FAIL:" << entry.path() << " " << smi1
<< " != " << smi2 << std::endl;
failed++;
// std::cerr << "molfile:" << smi1 << std::endl;
// std::cerr << "cdx :" << smi2 << std::endl;
// std::cerr << cdx << std::endl;
} else {
// std::cerr << "PASS:" << entry.path() << std::endl;
}
// CHECK(smi1 == smi2);
delete mol;
}
}
}
std::cerr << "Failed:" << failed << " out of " << total << std::endl;
REQUIRE(failed == 0);
}
}
TEST_CASE("Fragments") {
std::string path =
std::string(getenv("RDBASE")) + "/External/ChemDraw/test_data/";
SECTION("Single Atom Replacements") {
auto fname = path + "atom-to-fragment.cdxml";
auto mols = MolsFromChemDrawFile(fname);
REQUIRE(mols.size());
REQUIRE("CC=C=C(C)C" == MolToSmiles(*mols[0]));
}
}
TEST_CASE("Geometry") {
std::string path =
std::string(getenv("RDBASE")) + "/External/ChemDraw/test_data/";
SECTION("Single Atom Replacements") {
auto fname = path + "geometry-tetrahedral.cdxml";
auto mols = MolsFromChemDrawFile(fname);
REQUIRE(mols.size());
REQUIRE("C1[C@H]2C[C@@H]12" == MolToSmiles(*mols[0]));
}
}
TEST_CASE("Test Reading Wrong File Format") {
std::string path =
std::string(getenv("RDBASE")) + "/Code/GraphMol/test_data/CDXML/";
SECTION("CDX as CDXML") {
auto fname = path + "ring-stereo1.cdx";
ChemDrawParserParams params;
params.format = CDXFormat::CDXML;
bool caught = false;
try {
auto mols = MolsFromChemDrawFile(fname, params);
} catch (FileParseException &ex) {
caught = true;
}
REQUIRE(caught);
}
}
TEST_CASE("github8761") {
std::string path =
std::string(getenv("RDBASE")) + "/External/ChemDraw/test_data/";
SECTION("US12404367-20250902-C00017") {
auto fname = path + "US12404367-20250902-C00017.CDX";
auto mols = MolsFromChemDrawFile(fname);
REQUIRE(mols.size());
fname = path + "US12404367-20250902-C00025.CDX";
mols = MolsFromChemDrawFile(fname);
REQUIRE(mols.size());
}
SECTION("Failing Patents") {
std::filesystem::path patents(path + "patents");
for (auto &entry : std::filesystem::directory_iterator(patents)) {
ChemDrawParserParams params;
params.sanitize = false;
auto mols = MolsFromChemDrawFile(entry.path().generic_string(), params);
// we just don't want a crash
std::string block;
std::fstream chemdrawfile(entry.path(), std::ios::in | std::ios::binary);
std::stringstream buffer;
buffer << chemdrawfile.rdbuf();
mols = MolsFromChemDrawBlock(buffer.str(), params);
// we just don't want a crash
}
}
}
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