FAIRMol

Z57170530

ID 2155

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

SMILES: O=c1oc2ccccc2c(O)c1Cc1c(O)c2ccccc2oc1=O

Formula: C19H12O6 | MW: 336.29900000000004

LogP: 2.9014000000000006 | TPSA: 100.88000000000001

HBA/HBD: 6/2 | RotB: 2

InChIKey: DOBMPNYZJYQDGZ-UHFFFAOYSA-N

Recognized patterns

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

Bio motif

H-bond acceptor O ×4 H-bond donor ×2 Gatekeeper aromatic ×2

Functional group

Phenol ×2

Ring system

Benzene ×2 Coumarin ×2

Properties

NameValueUnit
DOCK_BASE_INTER_RANK-1.136250-
DOCK_BASE_INTER_RANK-1.240890-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_CLASH_COUNT14.000000-
DOCK_CLASH_COUNT13.000000-
DOCK_CONTACT_COUNT12.000000-
DOCK_CONTACT_COUNT14.000000-
DOCK_EXPERIMENTT05-
DOCK_EXPERIMENTT19-
DOCK_EXPERIMENT_ID5-
DOCK_EXPERIMENT_ID19-
DOCK_FINAL_RANK2.250412-
DOCK_FINAL_RANK3.992078-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOM_OK0-
DOCK_GEOM_OK0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_IFP::A:ARG171-
DOCK_IFP::A:GLY2251-
DOCK_IFP::A:LEU1881-
DOCK_IFP::A:LEU2261-
DOCK_IFP::A:LEU2291-
DOCK_IFP::A:NDP3021-
DOCK_IFP::A:PHE1131-
DOCK_IFP::A:SER1111-
DOCK_IFP::A:SER1121-
DOCK_IFP::A:TYR1941-
DOCK_IFP::A:VAL2301-
DOCK_IFP::C:ALA3381-
DOCK_IFP::C:ASP3271-
DOCK_IFP::C:CYS521-
DOCK_IFP::C:CYS571-
DOCK_IFP::C:GLY561-
DOCK_IFP::C:LEU3341-
DOCK_IFP::C:LYS601-
DOCK_IFP::C:MET3331-
DOCK_IFP::C:NDP8001-
DOCK_IFP::C:PHE3671-
DOCK_IFP::C:PRO3361-
DOCK_IFP::C:SER141-
DOCK_IFP::C:THR3351-
DOCK_IFP::C:THR511-
DOCK_IFP::D:ARG2871-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_MAX_CLASH_OVERLAP0.617146-
DOCK_MAX_CLASH_OVERLAP0.617168-
DOCK_POSE_COUNT1-
DOCK_POSE_COUNT1-
DOCK_PRE_RANK2.216313-
DOCK_PRE_RANK3.961571-
DOCK_PRIMARY_POSE_ID3073-
DOCK_PRIMARY_POSE_ID12561-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_REPORT_IDselection_import_t05-
DOCK_REPORT_IDselection_import_t19-
DOCK_RESIDUE_CONTACTSA:ARG17;A:GLY225;A:LEU188;A:LEU226;A:LEU229;A:NDP302;A:PHE113;A:SER111;A:SER112;A:TYR194;A:VAL230;D:ARG287-
DOCK_RESIDUE_CONTACTSC:ALA338;C:ASP327;C:CYS52;C:CYS57;C:GLY56;C:LEU334;C:LYS60;C:MET333;C:NDP800;C:PHE367;C:PRO336;C:SER14;C:THR335;C:THR51-
DOCK_SCAFFOLDO=c1oc2ccccc2cc1Cc1cc2ccccc2oc1=O-
DOCK_SCAFFOLDO=c1oc2ccccc2cc1Cc1cc2ccccc2oc1=O-
DOCK_SCORE-27.767200-
DOCK_SCORE-32.343200-
DOCK_SCORE_INTER-28.406300-
DOCK_SCORE_INTER-31.022200-
DOCK_SCORE_INTER_KCAL-6.784731-
DOCK_SCORE_INTER_KCAL-7.409528-
DOCK_SCORE_INTER_NORM-1.136250-
DOCK_SCORE_INTER_NORM-1.240890-
DOCK_SCORE_INTRA0.639137-
DOCK_SCORE_INTRA-2.485400-
DOCK_SCORE_INTRA_KCAL0.152655-
DOCK_SCORE_INTRA_KCAL-0.593628-
DOCK_SCORE_INTRA_NORM0.025566-
DOCK_SCORE_INTRA_NORM-0.099416-
DOCK_SCORE_KCAL-6.632085-
DOCK_SCORE_KCAL-7.725044-
DOCK_SCORE_NORM-1.110690-
DOCK_SCORE_NORM-1.293730-
DOCK_SCORE_RESTR0.000000-
DOCK_SCORE_RESTR1.164430-
DOCK_SCORE_RESTR_NORM0.000000-
DOCK_SCORE_RESTR_NORM0.046577-
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_FILET05_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FILET19_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FORMULAC19H12O6-
DOCK_SOURCE_FORMULAC19H12O6-
DOCK_SOURCE_HBA6.000000-
DOCK_SOURCE_HBA6.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HEAVY_ATOMS25.000000-
DOCK_SOURCE_HEAVY_ATOMS25.000000-
DOCK_SOURCE_LOGP2.901400-
DOCK_SOURCE_LOGP2.901400-
DOCK_SOURCE_MW336.299000-
DOCK_SOURCE_MW336.299000-
DOCK_SOURCE_NAMEZ57170530-
DOCK_SOURCE_NAMEZ57170530-
DOCK_SOURCE_RINGS4.000000-
DOCK_SOURCE_RINGS4.000000-
DOCK_SOURCE_TPSA100.880000-
DOCK_SOURCE_TPSA100.880000-
DOCK_STRAIN_DELTA26.154029-
DOCK_STRAIN_DELTA23.883378-
DOCK_STRAIN_OK1-
DOCK_STRAIN_OK1-
DOCK_TARGETT05-
DOCK_TARGETT19-
EXACT_MASS336.063388104Da
FORMULAC19H12O6-
HBA6-
HBD2-
LOGP2.9014000000000006-
MOL_WEIGHT336.29900000000004g/mol
QED_SCORE0.5459100356936089-
ROTATABLE_BONDS2-
TPSA100.88000000000001A^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
T05 T05 selection_import_t05 1
native pose available
 2.2504119895268624 -27.7672 11 0.65 - Best pose
T19 T19 selection_import_t19 1
native pose available
 3.9920777646348005 -32.3432 5 0.19 - Best pose
T05 — T05 1 poses · report selection_import_t05
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
363 2.2504119895268624 -1.13625 -27.7672 6 12 11 0.65 0.43 0.50 0.60 - no geometry warning; 14 clashes; 1 protein clash; 1 severe cofactor-context clash; moderate strain Δ 26.2 Open pose
T19 — T19 1 poses · report selection_import_t19
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
360 3.9920777646348005 -1.24089 -32.3432 9 14 5 0.19 0.08 0.20 0.25 - 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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