Introduction


We evaluated the molecular generation methods and generated molecules using PoseBusters[paper]. Considering that PoseBusters is also suitable for evaluating molecular docking methods, we only retained indicators that may have reference significance in molecular generation and displayed all evaluation results on this page.

Section 1: An Overview of PoseBusters


Section 2: PoseBusters Filter Waterfall


The moleculars that cannot be Kekuleized have been excluded.

Section 3: Detailed Test Result Search


id smiles method pdb id PB valid mol pred loaded mol true loaded mol cond loaded sanitization all atoms connected bond lengths bond angles internal steric clash aromatic ring flatness double bond flatness internal energy protein ligand maximum distance minimum distance to protein minimum distance to organic cofactors minimum distance to inorganic cofactors minimum distance to waters volume overlap with protein volume overlap with organic cofactors volume overlap with inorganic cofactors volume overlap with waters
38341 O=C1C(O)C(O)CC2=CC3=CC4=Cc5cc6ccc7ccccc7c6cc5CC4=CN3CN12 Pocket2Mol 1H36
38342 O=c1cc2n(c(=O)n1C(O)C(F)(F)F)C=C1CC=CC1C2 Pocket2Mol 1H36
38343 CN1C2=CC3CC(=O)N(C4CCNC4)C(=O)N3C=C2Cc2cc3c4c(ccc3cc21)CC=CC4 Pocket2Mol 1H36
38344 O=C(O)CC1COc2ccccc2C1 Pocket2Mol 1H36
38345 CCC1=CCc2c3c(c(=O)oc2=C1)=CC=C(C1=CCC2=CN4C(=O)N(C5CCNCN5)C=CC4=CC2=C1)C3 Pocket2Mol 1H36
38346 O=C1N2C=C3CCC(O)C3=CC2=CC2OCC3CC(CN3)N12 Pocket2Mol 1H36
38347 CC1=CC2(C=C1)Cc1cc(-c3ccnc(CNc4cc5ccncc5cc4O)c3)cc(C)c1C(=O)O2 Pocket2Mol 1H36
38348 O=C1[C@H](O)CO[C@H]2C[C@H]3CC4=CC(c5cccc(C=CC=C6C=CC=N6)c5)=CCC4=CN3CN12 Pocket2Mol 1H36
38349 O=C1OCC(=O)c2c(Cl)cccc21 Pocket2Mol 5ORJ
38350 Cc1cccc2c1CC=CC2=O Pocket2Mol 5ORJ
38351 CCC(C)(C=O)c1ccccc1 Pocket2Mol 5ORJ
38352 Cc1c(O)ccc2c1C=CCC2=O Pocket2Mol 5ORJ
38353 Cc1cccc2c1CC(O)CC2=O Pocket2Mol 5ORJ
38354 O=C1CC=Cc2c1ccc(O)c2O Pocket2Mol 5ORJ
38355 Cc1ccc2c(c1)CC=CO2 Pocket2Mol 5ORJ

38341 to 38355 of 73725 items. Total 4915 pages.