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
63931 CC1CC2CN3C(=O)CCC3c3cccc(c3)C3CCC4(CC1(C)C(O)C4=O)C23 TargetDiff 3B6H
63932 CC(=O)N1CN2C1c1ccccc1C(C)C(C)(O)N2C TargetDiff 3B6H
63933 CCCCc1ccccc1NC(C)C TargetDiff 3B6H
63934 CCC(C)(C)C1COC(C(=N)CC#N)C1 TargetDiff 3B6H
63935 CC1(O)CN(CO)C2C3C(O)CCC4C=CCC=C4C3NC21 TargetDiff 3B6H
63936 CC(CO)N1CCC2CC(=O)NC(C)(C)C2C2=C1CNN2 TargetDiff 3B6H
63937 CCC(C)(C)c1cccc(CC(=O)O)c1 TargetDiff 3B6H
63938 CC(C)CC(C)C=CCC(=O)O TargetDiff 3B6H
63939 OC1(N2N=CCC3=C=C2CC=CC3)CCc2ccccc21 TargetDiff 3B6H
63940 CCC(O)CN1CCC2CN(C(CO)c3ccccc31)C(C(O)CC)CO2 TargetDiff 3B6H
63941 CC1C(=O)NCCC(O)C(=O)NCC2C=CC(C=C2)C(O)C(O)C1C TargetDiff 3B6H
63942 C=[SH]P(OP(N)[PH](N)(N)CO)PS#[SH] TargetDiff 3B6H
63943 CC1C=C(COCC2CCC2)C(C)(C)CC1 TargetDiff 3B6H
63944 O=C(c1ccc(O)cc1Nc1ccccc1)N1CC2C=CCC1C2 TargetDiff 3B6H
63945 CCCC(CC1(C)CCC1C1(O)CCC2C(=O)CC(O)C21)C(C)C=O TargetDiff 3B6H

63931 to 63945 of 73725 items. Total 4915 pages.