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
51346 CN=Cc1cc2cc(C)ccc2nc1-c1cc(NC)[nH]n1 Pocket2Mol 1R1H
51347 CCCc1cccc(C2CCC(C)C(C(=O)NO)C2=O)c1 Pocket2Mol 1R1H
51348 Cc1ccc(C2C=C3N=CC(C(N)=O)=CN3C(=O)C2)cc1 Pocket2Mol 1R1H
51349 Cc1cc(C2=CCC=N2)ccc1C1NCC(C)(O)NC1O Pocket2Mol 1R1H
51350 Cc1ccc(-c2ccc3cc(C(=O)O)c(N)nc3c2)cc1 Pocket2Mol 1R1H
51351 NC(=O)c1cc2cnc(-c3ccc(Cl)cc3)cc2nc1N Pocket2Mol 1R1H
51352 CN=Cc1cc2cc(O)ccc2nc1-c1nnc(N)[nH]1 Pocket2Mol 1R1H
51353 CN=Cc1cc2cc(C)ccc2nc1C1=NNC(N)=NN1 Pocket2Mol 1R1H
51354 CC1=C(CC(=O)O)C=C2CC(=O)CC[SH]21 Pocket2Mol 1R1H
51355 CCOc1cccc2c1OC1CCOC23CC(N)CC13 Pocket2Mol 1R1H
51356 CC1=CC(O)=C(c2ccc3[nH]c(=O)c(N)nc3c2)OC1 Pocket2Mol 1R1H
51357 CCc1cc2c(cc1NC(=O)C(=O)NC)CCC(O)O2 Pocket2Mol 1R1H
51358 CCC(C)n1cc2cc(C)cc(OP(=O)(O)O)c2cc1=O Pocket2Mol 1R1H
51359 Cc1ccc(-c2cc3nc(N)c(C(=O)O)cc3cn2)cc1 Pocket2Mol 1R1H
51360 O=c1c2c(oc3ccccc13)CCC1(O)CCC(O)C21O Pocket2Mol 1R1H

51346 to 51360 of 73725 items. Total 4915 pages.