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
30676 CC1(C2CCC3NC3C2)CCNC1 GraphBP 6G2B
30677 CCCCC1CCCCC(N)(F)OC1=O GraphBP 6G2B
30678 C=NCC1CC12C1CC12C1(C)CC1(O)C1C(OC(C)C)CC2(CCCl)CN(CCC34CC(C(C)C)CC5(CCC5C)NC3C4)C12 GraphBP 6G2B
30679 OCC1(C23OC2C2CC23)CC1 GraphBP 6G2B
30680 CC(O)C(CCC(O)NO)C1CN1 GraphBP 6G2B
30681 NCOC1(O)C2NC23C1ON3C1C2CCC21 GraphBP 6G2B
30682 C=C(CC)CC(C)CC(C)CCO GraphBP 6G2B
30683 OOC(C1CC1)C12NC1(F)C2Cl GraphBP 6G2B
30684 C#CCCCC(CCC(=C)C(C)C1CCC1CCCC(C)C(Cl)CC)CC12C(C=C)C(C=C)CC1C21NC1CC GraphBP 6G2B
30685 CCCC(O)C1OCCC23CC2C13 GraphBP 6G2B
30686 C=CCCC1CC(C)C(C2SCC2(C)CC(CCCC)C(C=C)C2CC2)C1C(Cl)CCCC(CC=C)CCC(N)C[N]C[NH] GraphBP 6G2B
30687 CCC(CC(C(CN)CCO)C12CC1C(CCCOCN)CCCC2CCC1OCC=C1C)C(CC=N)C1CCCCC1C GraphBP 6G2B
30688 COC(=O)CCC1C2CC(C)C3CC4CCC4C(CN)C(C3)C3CC3C12 GraphBP 6G2B
30689 C1=CC2CC23C2CC23N1 GraphBP 5VCZ
30690 CN(C1N2C3NNC312)C(N)([O])[Mg] GraphBP 5VCZ

30676 to 30690 of 73725 items. Total 4915 pages.