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
23716 [C][C][C][C]1[C]ON2[C][C]([C])C(=NO2)[C]2[C](N3[N][C]3[C])N2[C]1 DiffSBDD 5OD1
23717 [O]N1[C]2[N]N=C([N][C]3[C][C]3)[C]21 DiffSBDD 5OD1
23718 [C][C][C][C]1C2([C]C2=O)[C@]1([C][O])N1[C][C@]12[C]([C])[C]2N=[C] DiffSBDD 5OD1
23719 [C][C]([C])[C]1[C][C]1[C]=O DiffSBDD 5OD1
23720 [O][C]1[C][C][C]2[C]3[N][C@]34[C]([O])[C]4O[C]C2=[C]1 DiffSBDD 5OD1
23721 [N]=C([C][N][C]1[C]C12[C][C]2)[C]1[C][C]1 DiffSBDD 5OD1
23722 [C]=[C][C]1[C]([O])[C]2[C][C]2[C@@]1([N])O[N][O] DiffSBDD 5OD1
23723 [C][C]([C]([O])[C]([C][C]([O])[C]=C=O)[N][O])[C](C#[S])[C@@]1([C])[N]C12[C][C]2 DiffSBDD 5OD1
23724 [C][C][C]([N])[C@@]1([C]=O)[C]([C]2[C](C([O])([O])[C]3[C][N]3)N2[O])C1=[P] DiffSBDD 5OD1
23725 [C][C]N1[C][C][C][C][C]([C]2[C](C(=S)[C][C][O])[C@]23[C]([N])[C]3[O])C1=[C] DiffSBDD 5OD1
23726 [C][C]1[C][C][C]([C][C]2[C][C]([O])[P]2)[C]N([C]=O)[C]([C])[C][C]1 DiffSBDD 6HAX
23727 [C][C]([C][C]([C][C][O])C(=[C])[O])[C]=C=[C][C][C]1[C]([C])[C@]1(O[O])[C]([C])[C]O[O] DiffSBDD 6HAX
23728 [C]=C1[C](OC([O])=O)[C@]12[C][C]2[C]1[C][C]1[O] DiffSBDD 6HAX
23729 [C]O[C]([C]=[C])[C@@]1(Cl)[C]N1N([O])OC(=O)[C]1[C]O[C]2O[C]21 DiffSBDD 6HAX
23730 [C][C][C]1[C][C](/[C]=N/[C]([C]([C])[O])[C@@]23[C][C@]24[C]([N][N]O[C])[C]43)[C][C]1[C] DiffSBDD 6HAX

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