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
46351 NS(=O)(=O)N1CCC(=O)C1 Pocket2Mol 5MJN
46352 N=C(N)CCC1CN=C2CCC(O)=C(C(=O)O)C2N1 Pocket2Mol 4POW
46353 CN(C)C(=O)[C@@H](C=CC1=C[C@@H](O)CN1)CC(=O)O Pocket2Mol 4POW
46354 CC(=O)NC(C(=O)O)c1cnc2ncccc2n1 Pocket2Mol 4POW
46355 O=C(CO)NC(C(=O)O)c1cnc2ncccc2n1 Pocket2Mol 4POW
46356 CN1CC[C@@H](C(=O)O)[C@H](C=CC2=CC(=O)CN2)C1=O Pocket2Mol 4POW
46357 c1ccncc1 Pocket2Mol 4POW
46358 CN1CC[C@@H](C(=O)O)[C@H](C=CC2=C[C@@H](O)CN2)C1=O Pocket2Mol 4POW
46359 CN1CC[C@@H](C(=O)O)[C@H](C=CC2=CCC(=O)N2)C1=O Pocket2Mol 4POW
46360 CC1CC(O)C(N2CC=C(C(=O)O)C2)O1 Pocket2Mol 4URY
46361 Cc1coc(-c2ccc3c(c2O)CCO3)c1 Pocket2Mol 4URY
46362 Cc1cc(-c2ccc3c(c2O)CCO3)on1 Pocket2Mol 4URY
46363 CCCNC(=O)CN1CC=C(C(=O)O)C1 Pocket2Mol 4URY
46364 Cn1cccc1C(N)=O Pocket2Mol 6QE5
46365 NC(=O)c1ccccc1N Pocket2Mol 6QE5

46351 to 46365 of 73725 items. Total 4915 pages.