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
35716 Cc1cccc(C(=O)O)c1-c1cc(C(=O)O)n2c1C(C)(C)CCC2 Pocket2Mol 1D7J
35717 Cn1c(=O)c2ccccc2c2cc(O)ccc21 Pocket2Mol 1D7J
35718 Cc1ccc(CO)cc1CCCCN1C(=O)COc2c(O)cccc21 Pocket2Mol 1D7J
35719 CC1c2c(-c3ccc(F)cc3)cc(-c3ccc(O)cc3O)n2CCC1(C)C Pocket2Mol 1D7J
35720 Cc1cccc(C(=O)O)c1-c1cc(C(=O)O)n2c1C(C)CCC2 Pocket2Mol 1D7J
35721 Cc1ccc(C)c(CCCCN2CCCC(C(=O)O)C2=O)c1 Pocket2Mol 1D7J
35722 OC1CCC2CCC3CCC4C(O)CC1=C2N34 Pocket2Mol 1D7J
35723 CC1(C)CCN(CCC(=O)O)CC1C(=O)O Pocket2Mol 1D7J
35724 CC(C)(C)c1ccc2c(n1)C1C(=CC=C2)C2CCC3CCC1(C(=O)O)CC32 Pocket2Mol 1D7J
35725 Cc1ccc(O)c(-c2cc(-c3ccccc3)c3n2CCC(C)(C)C3C)c1 Pocket2Mol 1D7J
35726 Cc1ccc2c(c1)C(C1CCC(C)(C)CN1C)C=NC2 Pocket2Mol 1D7J
35727 CC1N=C(CC(=O)O)N2CCCCC12 Pocket2Mol 1D7J
35728 Oc1ccc(O)c(-c2cc(-c3ccccc3)c3n2CC2CCC3CC2)c1 Pocket2Mol 1D7J
35729 O=C1CC(C(=O)O)c2cccc(c2)-c2cccc(CO)c2OC(=O)CN1 Pocket2Mol 1D7J
35730 CN(C)C(=O)CC1NCCN2CC3OCC(=O)NCC3CC12 Pocket2Mol 1D7J

35716 to 35730 of 73725 items. Total 4915 pages.