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
30706 C=C1OCC2C3OC4C5CC67C8C69CC9OC6(C(=C)C(C)(C)C)C(C1COCCC(C(C)C)CC1CCC(C1)C23)C6C4C587 GraphBP 5VCZ
30707 CC(F)C1NC1C1CC1C1OC23CC45CC4C5(NCl)C4C5C6C5C57C6C5(O)C47C2C13 GraphBP 5VCZ
30708 C=C(C)C[C@H]1CN1[C@@H]1CNN1C=NCCCC GraphBP 5VD2
30709 C=C(C)CCCCCOO GraphBP 5VD2
30710 O=C(O)C(O)CO GraphBP 5VD2
30711 CCCCC(COCCCOCC)C(C)C(C)(C)O GraphBP 5VD2
30712 CCCCC1C2C(CC)C2C2C3CCC(C4CC5(CCCCC6CC6C(C)C)COC6C(CC6(N)N)C45)C1C32 GraphBP 5VD2
30713 NC(=O)CC1(CO)OC1O GraphBP 5VD2
30714 C=C(COC[SiH2]O)C1CC=CC2C(OC(=O)CC=O)CC(C)C(C)C12 GraphBP 5VD2
30715 CCCCC1C(C2CC3C4CC35C(ONC3C(C=C=C(F)C(F)CCNCC)C3(C)CO2)C5C4CCC)C2CC(C)(F)C12 GraphBP 5VD2
30716 CC(CC1OCO1)C1CNC1 GraphBP 5VD2
30717 CCOC1(C)OC1C(C)(CC)CCC(C)CC1CC1 GraphBP 5VD2
30718 CC1[N]C12CCNC(NNC1CC1O)[N]2 GraphBP 5VD2
30719 OC1OC1CC1CC12CC2 GraphBP 5VD2
30720 C=CC1CCCC(CCCCC(C)(CC(C)NCC(C)O)C23C4CC4CC24CC43)C1C GraphBP 5VD2

30706 to 30720 of 73725 items. Total 4915 pages.