FAIRMol

OSA_Lib_54

ID 473

DB SELECTIONThis detail page is pinned to the current database context.
Back to results Open docking pose (2)
2D structure

SMILES: [NH3+]CC(=O)O[C@H]1C[C@@]2([NH+]3CCCC3)C[C@H](c3ccccc3)[C@@H]1[C@H](c1ccccc1)C2

Formula: C26H34N2O2+2 | MW: 406.57000000000005

LogP: 1.9389000000000007 | TPSA: 58.379999999999995

HBA/HBD: 2/2 | RotB: 5

InChIKey: QRCGKZHMDVRFJM-RXDLHWJPSA-P

Recognized patterns

Click a named motif to highlight it in the 2D depiction or launch reverse search.
Highlighted: 1 pattern Metal chelator Clear highlight

Bio motif

H-bond acceptor N H-bond acceptor O ×2 H-bond donor ×2 Gatekeeper aromatic ×2 Metal chelator

Functional group

Carbonyl Ester Ether

Ring system

Benzene ×2 Pyrrolidine Cyclohexane ×3

Properties

NameValueUnit
DOCK_BASE_INTER_RANK-0.930722-
DOCK_BASE_INTER_RANK-0.880381-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_CLASH_COUNT14.000000-
DOCK_CLASH_COUNT13.000000-
DOCK_CONTACT_COUNT19.000000-
DOCK_CONTACT_COUNT14.000000-
DOCK_EXPERIMENTT01-
DOCK_EXPERIMENTT15-
DOCK_EXPERIMENT_ID1-
DOCK_EXPERIMENT_ID15-
DOCK_FINAL_RANK2.712986-
DOCK_FINAL_RANK4.955642-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOM_OK0-
DOCK_GEOM_OK0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_IFP::A:ALA101-
DOCK_IFP::A:GLU311-
DOCK_IFP::A:GLY1171-
DOCK_IFP::A:ILE1151-
DOCK_IFP::A:ILE611-
DOCK_IFP::A:ILE81-
DOCK_IFP::A:LEU231-
DOCK_IFP::A:LEU281-
DOCK_IFP::A:LEU681-
DOCK_IFP::A:NAP2011-
DOCK_IFP::A:PHE321-
DOCK_IFP::A:PHE351-
DOCK_IFP::A:PRO271-
DOCK_IFP::A:SER601-
DOCK_IFP::A:THR571-
DOCK_IFP::A:TRP251-
DOCK_IFP::A:TYR1221-
DOCK_IFP::A:VAL1161-
DOCK_IFP::A:VAL91-
DOCK_IFP::B:ALA901-
DOCK_IFP::B:ASN911-
DOCK_IFP::B:GLY2141-
DOCK_IFP::B:GLY2151-
DOCK_IFP::B:LYS2111-
DOCK_IFP::B:LYS891-
DOCK_IFP::B:MET701-
DOCK_IFP::B:PRO1871-
DOCK_IFP::B:PRO2121-
DOCK_IFP::B:PRO2131-
DOCK_IFP::B:SER861-
DOCK_IFP::B:TRP921-
DOCK_IFP::B:TYR2101-
DOCK_IFP::B:VAL881-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_MAX_CLASH_OVERLAP0.743256-
DOCK_MAX_CLASH_OVERLAP0.743328-
DOCK_POSE_COUNT1-
DOCK_POSE_COUNT1-
DOCK_PRE_RANK2.675999-
DOCK_PRE_RANK4.925164-
DOCK_PRIMARY_POSE_ID201-
DOCK_PRIMARY_POSE_ID9660-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_REPORT_IDselection_import_t01-
DOCK_REPORT_IDselection_import_t15-
DOCK_RESIDUE_CONTACTSA:ALA10;A:GLU31;A:GLY117;A:ILE115;A:ILE61;A:ILE8;A:LEU23;A:LEU28;A:LEU68;A:NAP201;A:PHE32;A:PHE35;A:PRO27;A:SER60;A:THR57;A:TRP25;A:TYR122;A:VAL116;A:VAL9-
DOCK_RESIDUE_CONTACTSB:ALA90;B:ASN91;B:GLY214;B:GLY215;B:LYS211;B:LYS89;B:MET70;B:PRO187;B:PRO212;B:PRO213;B:SER86;B:TRP92;B:TYR210;B:VAL88-
DOCK_SCAFFOLDc1ccc(C2CC3([NH+]4CCCC4)CCC2C(c2ccccc2)C3)cc1-
DOCK_SCAFFOLDc1ccc(C2CC3([NH+]4CCCC4)CCC2C(c2ccccc2)C3)cc1-
DOCK_SCORE-20.023900-
DOCK_SCORE-25.681800-
DOCK_SCORE_INTER-27.921700-
DOCK_SCORE_INTER-26.411400-
DOCK_SCORE_INTER_KCAL-6.668986-
DOCK_SCORE_INTER_KCAL-6.308257-
DOCK_SCORE_INTER_NORM-0.930722-
DOCK_SCORE_INTER_NORM-0.880381-
DOCK_SCORE_INTRA7.897800-
DOCK_SCORE_INTRA0.729152-
DOCK_SCORE_INTRA_KCAL1.886358-
DOCK_SCORE_INTRA_KCAL0.174155-
DOCK_SCORE_INTRA_NORM0.263260-
DOCK_SCORE_INTRA_NORM0.024305-
DOCK_SCORE_KCAL-4.782628-
DOCK_SCORE_KCAL-6.133995-
DOCK_SCORE_NORM-0.667462-
DOCK_SCORE_NORM-0.856059-
DOCK_SCORE_RESTR0.000000-
DOCK_SCORE_RESTR0.000499-
DOCK_SCORE_RESTR_NORM0.000000-
DOCK_SCORE_RESTR_NORM0.000017-
DOCK_SCORE_SYSTEM0.000000-
DOCK_SCORE_SYSTEM0.000000-
DOCK_SCORE_SYSTEM_NORM0.000000-
DOCK_SCORE_SYSTEM_NORM0.000000-
DOCK_SELECTION_EXCLUDED0-
DOCK_SELECTION_EXCLUDED0-
DOCK_SEVERE_CLASH_COUNT0.000000-
DOCK_SEVERE_CLASH_COUNT0.000000-
DOCK_SOURCE_FILET01_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FILET15_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FORMULAC26H34N2O2+2-
DOCK_SOURCE_FORMULAC26H34N2O2+2-
DOCK_SOURCE_HBA2.000000-
DOCK_SOURCE_HBA2.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HEAVY_ATOMS30.000000-
DOCK_SOURCE_HEAVY_ATOMS30.000000-
DOCK_SOURCE_LOGP1.938900-
DOCK_SOURCE_LOGP1.938900-
DOCK_SOURCE_MW406.570000-
DOCK_SOURCE_MW406.570000-
DOCK_SOURCE_NAMEOSA_Lib_54-
DOCK_SOURCE_NAMEOSA_Lib_54-
DOCK_SOURCE_RINGS6.000000-
DOCK_SOURCE_RINGS6.000000-
DOCK_SOURCE_TPSA58.380000-
DOCK_SOURCE_TPSA58.380000-
DOCK_STRAIN_DELTA27.871293-
DOCK_STRAIN_DELTA23.864200-
DOCK_STRAIN_OK1-
DOCK_STRAIN_OK1-
DOCK_TARGETT01-
DOCK_TARGETT15-
EXACT_MASS406.26093116818Da
FORMULAC26H34N2O2+2-
HBA2-
HBD2-
LOGP1.9389000000000007-
MOL_WEIGHT406.57000000000005g/mol
QED_SCORE0.7458827171489573-
ROTATABLE_BONDS5-
TPSA58.379999999999995A^2

Docking across targets

This compound is global in the current database. Below you can review all docking experiments and targets that contain imported poses for it, which is the basis for reverse docking analysis.

Open primary docking pose Docking experiments Reverse docking explorer Protein structures Docking IFP projection
TargetExperimentReportPosesBest rankBest scoreNative overlapNative recallRMSD
T01 T01 selection_import_t01 1
native pose available
 2.7129855355548504 -20.0239 15 0.71 - Best pose
T15 T15 selection_import_t15 1
native pose available
 4.9556415628837795 -25.6818 7 0.54 - Best pose
T01 — T01 1 poses · report selection_import_t01
Native comparison is calculated against the uploaded native ligand for the same experiment/target whenever it is available.
PoseFinal rankInter normScoreHBContactsNative overlapNative recallHB strictHB roleHB residueRMSDExcludedNotes
201 2.7129855355548504 -0.930722 -20.0239 4 19 15 0.71 0.60 0.60 0.60 - no geometry warning; 14 clashes; 1 protein clash; moderate strain Δ 27.9 Open pose
T15 — T15 1 poses · report selection_import_t15
Native comparison is calculated against the uploaded native ligand for the same experiment/target whenever it is available.
PoseFinal rankInter normScoreHBContactsNative overlapNative recallHB strictHB roleHB residueRMSDExcludedNotes
174 4.9556415628837795 -0.880381 -25.6818 4 14 7 0.54 - - - - no geometry warning; 13 clashes; 3 protein clashes; moderate strain Δ 23.9 Open pose
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Drug Similarity

Shared structural fragments with approved drugs — based on faircheckmol profile fingerprint.
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Structural Profile Fingerprint

Named-bit fingerprint from curated SMARTS patterns. Each bit = one chemical pattern.

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ADMET Profile

Computed from structure using RDKit. Indicative only — not a substitute for experimental data.

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3D Conformer

ETKDGv3 conformer generation with UFF minimisation. Rendered with 3Dmol.js.

Open receptor–ligand complex
This docking hit has a stored pose-level complex analysis page with clickable hydrogen bonds, π–π contacts, hydrophobic contacts, and clash inspection.
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