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
40816 NC1=NC2=NCC=C3CCc4ccc5c(N)cnn5c4C1=C32 Pocket2Mol 5KO1
40817 Cc1ccc2c(n1)N=C(N)C2c1cnc[nH]1 Pocket2Mol 5KO1
40818 N=C(N)C=CC1=C[C@H]([C@@H](N)C(=O)O)C[C@@H](O)C1=O Pocket2Mol 5OT8
40819 N[C@@H](C(=O)O)[C@H]1C=C(C=CC(=O)O)C(=O)[C@@H](O)C1 Pocket2Mol 5OT8
40820 N[C@@H](C(=O)O)[C@H]1C=C(C=CC(=O)O)C(=O)C(=O)C1 Pocket2Mol 5OT8
40821 N=C(N)C=CC1=C[C@H]([C@@H](N)C(=O)O)CC(=O)C1=O Pocket2Mol 5OT8
40822 O=C(C=CO[C@H](COC(=O)O)C(=O)O)CO Pocket2Mol 5OT8
40823 COc1ccc2c(c1)C(N)CNC2CO Pocket2Mol 4CPY
40824 NC1CNC(CO)c2cc(O)c(O)cc21 Pocket2Mol 4CPY
40825 CN1CC(N)c2cc(O)ccc2C1CO Pocket2Mol 4CPY
40826 O=C(O)CCC1=CC(O)CC2C=CCC12 Pocket2Mol 4CPY
40827 O=C(O)CCC1=CC(O)CC2CCCC12 Pocket2Mol 4CPY
40828 O=C1c2ccccc2CCN1Cc1ccc(O)cc1O Pocket2Mol 5BW4
40829 O=C1c2ccccc2NCN1Cc1ccc(O)cc1O Pocket2Mol 5BW4
40830 O=C(O)c1ccc2c(c1)CN(Cc1ccc(O)cc1O)C=C2 Pocket2Mol 5BW4

40816 to 40830 of 73725 items. Total 4915 pages.