// // Substructure searching with stereochemistry - example15.cpp #include #include #include #include int main( int argc , char **argv ) { RDKit::ROMOL_SPTR mol1( RDKit::SmilesToMol( "CC[C@H](F)Cl" ) ); RDKit::RWMOL_SPTR patt1( RDKit::SmartsToMol( "C[C@H](F)Cl" ) ); RDKit::MatchVectType res; if( RDKit::SubstructMatch( *mol1 , *patt1 , res ) ) { std::cout << "SMARTS 1 match" << std::endl; } else { std::cout << "Not SMARTS 1 match" << std::endl; } RDKit::RWMOL_SPTR patt2( RDKit::SmartsToMol( "C[C@@H](F)Cl" ) ); if( RDKit::SubstructMatch( *mol1 , *patt2 , res ) ) { std::cout << "SMARTS 2 match" << std::endl; } else { std::cout << "Not SMARTS 2 match" << std::endl; } RDKit::RWMOL_SPTR patt3( RDKit::SmartsToMol( "CC(F)Cl" ) ); if( RDKit::SubstructMatch( *mol1 , *patt3 , res ) ) { std::cout << "SMARTS 3 match" << std::endl; } else { std::cout << "Not SMARTS 3 match" << std::endl; } if( RDKit::SubstructMatch( *mol1 , *patt1 , res , true , true ) ) { std::cout << "SMARTS 1 chiral match" << std::endl; } else { std::cout << "Not SMARTS 1 chiral match" << std::endl; } if( RDKit::SubstructMatch( *mol1 , *patt2 , res , true , true ) ) { std::cout << "SMARTS 2 chiral match" << std::endl; } else { std::cout << "Not SMARTS 2 chiral match" << std::endl; } if( RDKit::SubstructMatch( *mol1 , *patt3 , res , true , true ) ) { std::cout << "SMARTS 3 chiral match" << std::endl; } else { std::cout << "Not SMARTS 3 chiral match" << std::endl; } RDKit::RWMOL_SPTR mol2( RDKit::SmilesToMol( "CC(F)Cl" ) ); if( RDKit::SubstructMatch( *mol1 , *mol2 , res , true , true ) ) { std::cout << "Chiral mol, non-chiral query : match" << std::endl; } else { std::cout << "Chiral mol, non-chiral query : NO match" << std::endl; } RDKit::RWMOL_SPTR patt5( RDKit::SmilesToMol( "C[C@H](F)Cl" ) ); if( RDKit::SubstructMatch( *mol2 , *patt5 , res , true , true ) ) { std::cout << "Non-chiral mol, chiral query : match" << std::endl; } else { std::cout << "Non-chiral mol, chiral query : NO match" << std::endl; } }