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
30946 CC1CC2CC23C1C3C1C2(CC3CC4C3C35C(C)C3(CCCl)C45)C3CC312 GraphBP 5J0D
30947 CCCC1NC2C(CC(C3CC4CC4CCC4CC3C4)C2C(C)CCC2CCC(C)CCCCC(CC)CC2CC)C2CC12 GraphBP 5J0D
30948 O=C1OC(O)CC(O)C1O GraphBP 5J0D
30949 OC12CC(CCC3C4CC34S)CC13CCC23 GraphBP 5NK4
30950 CC1C2C(C3CC3)CC12COO GraphBP 5NK4
30951 C=CC(C)C(CNC12CC(/C=C\CC3CN3C(C)N/C(C=N)=N\1)N2)COCCC GraphBP 5NK4
30952 OC12CCC(CC1)C(C1CNC3CC31)CC(F)C2 GraphBP 5NK4
30953 OC12CC1(F)C1CCC3C(CCCC4CC5(OOC52)C43)CC23CC2N13 GraphBP 5NK4
30954 CCCCC1CC1 GraphBP 5NK4
30955 CC(C(O)C1OC2(O)C(O)C12O)C1CC23NC12C3CCCC1CC1 GraphBP 5NK4
30956 OOC(CC1OC1O)CC1C2C(CCC3CC3)C12 GraphBP 5NK4
30957 CCCCC1CC1OC1CC(O)C1C(=O)O GraphBP 5NK4
30958 CCCC1CC(CCCCCC(C)(F)C2CO2)S1 GraphBP 5NK4
30959 C=CCC1CC(C(C)C=C)C2CC1CC(OC)C1CCC3CCC(C(C)CC1CC(C)NC2C)C(NC1C2C4(C)C(CC)C124)O3 GraphBP 5NK4
30960 C1=CC(C2C3C4CC423)C2CC2C1 GraphBP 5NK4

30946 to 30960 of 73725 items. Total 4915 pages.