FAIRMol

Z56842660

ID 91

DB SELECTIONThis detail page is pinned to the current database context.
Back to results Open docking pose (3)
2D structure

SMILES: CNc1sc(C(=O)c2ccccc2F)c(N)c1-c1nc2ccccc2s1

Formula: C19H14FN3OS2 | MW: 383.47300000000007

LogP: 5.0188000000000015 | TPSA: 68.01

HBA/HBD: 6/2 | RotB: 4

InChIKey: CDDOMAQODCBJKI-UHFFFAOYSA-N

Recognized patterns

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

Bio motif

H-bond acceptor N H-bond acceptor O H-bond donor ×2 Gatekeeper aromatic ×2 Ionizable base ×2

Functional group

Carbonyl Ketone Primary amine Secondary amine Fluorine

Ring system

Benzene ×2 Thiophene Benzothiazole Thiazole

Properties

NameValueUnit
DOCK_BASE_INTER_RANK-1.015490-
DOCK_BASE_INTER_RANK-1.011040-
DOCK_BASE_INTER_RANK-0.923793-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_CLASH_COUNT8.000000-
DOCK_CLASH_COUNT9.000000-
DOCK_CLASH_COUNT8.000000-
DOCK_CONTACT_COUNT13.000000-
DOCK_CONTACT_COUNT13.000000-
DOCK_CONTACT_COUNT15.000000-
DOCK_EXPERIMENTT01-
DOCK_EXPERIMENTT02-
DOCK_EXPERIMENTT16-
DOCK_EXPERIMENT_ID1-
DOCK_EXPERIMENT_ID2-
DOCK_EXPERIMENT_ID16-
DOCK_FINAL_RANK0.909412-
DOCK_FINAL_RANK1.018529-
DOCK_FINAL_RANK1.504259-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOM_OK0-
DOCK_GEOM_OK0-
DOCK_GEOM_OK0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_IFP::A:ALA101-
DOCK_IFP::A:ALA101-
DOCK_IFP::A:ALA2091-
DOCK_IFP::A:ALA901-
DOCK_IFP::A:ARG291-
DOCK_IFP::A:ARG291-
DOCK_IFP::A:ASN911-
DOCK_IFP::A:GLU311-
DOCK_IFP::A:GLU311-
DOCK_IFP::A:GLY2141-
DOCK_IFP::A:GLY2151-
DOCK_IFP::A:ILE81-
DOCK_IFP::A:ILE81-
DOCK_IFP::A:LEU231-
DOCK_IFP::A:LEU231-
DOCK_IFP::A:LEU281-
DOCK_IFP::A:LEU281-
DOCK_IFP::A:LYS2111-
DOCK_IFP::A:LYS891-
DOCK_IFP::A:LYS931-
DOCK_IFP::A:MET701-
DOCK_IFP::A:NAP2011-
DOCK_IFP::A:NAP2011-
DOCK_IFP::A:PHE321-
DOCK_IFP::A:PHE321-
DOCK_IFP::A:PHE351-
DOCK_IFP::A:PHE351-
DOCK_IFP::A:PRO1871-
DOCK_IFP::A:PRO2121-
DOCK_IFP::A:PRO2131-
DOCK_IFP::A:PRO271-
DOCK_IFP::A:PRO271-
DOCK_IFP::A:THR1371-
DOCK_IFP::A:THR1371-
DOCK_IFP::A:TRP921-
DOCK_IFP::A:TYR1221-
DOCK_IFP::A:TYR1221-
DOCK_IFP::A:TYR2101-
DOCK_IFP::A:VAL881-
DOCK_IFP::A:VAL91-
DOCK_IFP::A:VAL91-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_MAX_CLASH_OVERLAP0.623508-
DOCK_MAX_CLASH_OVERLAP0.623579-
DOCK_MAX_CLASH_OVERLAP0.623534-
DOCK_POSE_COUNT1-
DOCK_POSE_COUNT1-
DOCK_POSE_COUNT1-
DOCK_PRE_RANK0.854527-
DOCK_PRE_RANK0.962689-
DOCK_PRE_RANK1.460557-
DOCK_PRIMARY_POSE_ID571-
DOCK_PRIMARY_POSE_ID1238-
DOCK_PRIMARY_POSE_ID10733-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_REPORT_IDselection_import_t01-
DOCK_REPORT_IDselection_import_t02-
DOCK_REPORT_IDselection_import_t16-
DOCK_RESIDUE_CONTACTSA:ALA10;A:ARG29;A:GLU31;A:ILE8;A:LEU23;A:LEU28;A:NAP201;A:PHE32;A:PHE35;A:PRO27;A:THR137;A:TYR122;A:VAL9-
DOCK_RESIDUE_CONTACTSA:ALA10;A:ARG29;A:GLU31;A:ILE8;A:LEU23;A:LEU28;A:NAP201;A:PHE32;A:PHE35;A:PRO27;A:THR137;A:TYR122;A:VAL9-
DOCK_RESIDUE_CONTACTSA:ALA209;A:ALA90;A:ASN91;A:GLY214;A:GLY215;A:LYS211;A:LYS89;A:LYS93;A:MET70;A:PRO187;A:PRO212;A:PRO213;A:TRP92;A:TYR210;A:VAL88-
DOCK_SCAFFOLDO=C(c1ccccc1)c1cc(-c2nc3ccccc3s2)cs1-
DOCK_SCAFFOLDO=C(c1ccccc1)c1cc(-c2nc3ccccc3s2)cs1-
DOCK_SCAFFOLDO=C(c1ccccc1)c1cc(-c2nc3ccccc3s2)cs1-
DOCK_SCORE-27.467300-
DOCK_SCORE-27.374800-
DOCK_SCORE-24.389200-
DOCK_SCORE_INTER-26.402800-
DOCK_SCORE_INTER-26.287100-
DOCK_SCORE_INTER-24.018600-
DOCK_SCORE_INTER_KCAL-6.306203-
DOCK_SCORE_INTER_KCAL-6.278569-
DOCK_SCORE_INTER_KCAL-5.736747-
DOCK_SCORE_INTER_NORM-1.015490-
DOCK_SCORE_INTER_NORM-1.011040-
DOCK_SCORE_INTER_NORM-0.923793-
DOCK_SCORE_INTRA-1.064500-
DOCK_SCORE_INTRA-1.087710-
DOCK_SCORE_INTRA-0.370559-
DOCK_SCORE_INTRA_KCAL-0.254252-
DOCK_SCORE_INTRA_KCAL-0.259795-
DOCK_SCORE_INTRA_KCAL-0.088507-
DOCK_SCORE_INTRA_NORM-0.040942-
DOCK_SCORE_INTRA_NORM-0.041835-
DOCK_SCORE_INTRA_NORM-0.014252-
DOCK_SCORE_KCAL-6.560455-
DOCK_SCORE_KCAL-6.538361-
DOCK_SCORE_KCAL-5.825263-
DOCK_SCORE_NORM-1.056440-
DOCK_SCORE_NORM-1.052880-
DOCK_SCORE_NORM-0.938045-
DOCK_SCORE_RESTR0.000000-
DOCK_SCORE_RESTR0.000000-
DOCK_SCORE_RESTR0.000000-
DOCK_SCORE_RESTR_NORM0.000000-
DOCK_SCORE_RESTR_NORM0.000000-
DOCK_SCORE_RESTR_NORM0.000000-
DOCK_SCORE_SYSTEM0.000000-
DOCK_SCORE_SYSTEM0.000000-
DOCK_SCORE_SYSTEM0.000000-
DOCK_SCORE_SYSTEM_NORM0.000000-
DOCK_SCORE_SYSTEM_NORM0.000000-
DOCK_SCORE_SYSTEM_NORM0.000000-
DOCK_SELECTION_EXCLUDED0-
DOCK_SELECTION_EXCLUDED0-
DOCK_SELECTION_EXCLUDED0-
DOCK_SEVERE_CLASH_COUNT0.000000-
DOCK_SEVERE_CLASH_COUNT0.000000-
DOCK_SEVERE_CLASH_COUNT0.000000-
DOCK_SOURCE_FILET01_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FILET02_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FILET16_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FORMULAC19H14FN3OS2-
DOCK_SOURCE_FORMULAC19H14FN3OS2-
DOCK_SOURCE_FORMULAC19H14FN3OS2-
DOCK_SOURCE_HBA6.000000-
DOCK_SOURCE_HBA6.000000-
DOCK_SOURCE_HBA6.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HEAVY_ATOMS26.000000-
DOCK_SOURCE_HEAVY_ATOMS26.000000-
DOCK_SOURCE_HEAVY_ATOMS26.000000-
DOCK_SOURCE_LOGP5.018800-
DOCK_SOURCE_LOGP5.018800-
DOCK_SOURCE_LOGP5.018800-
DOCK_SOURCE_MW383.473000-
DOCK_SOURCE_MW383.473000-
DOCK_SOURCE_MW383.473000-
DOCK_SOURCE_NAMEZ56842660-
DOCK_SOURCE_NAMEZ56842660-
DOCK_SOURCE_NAMEZ56842660-
DOCK_SOURCE_RINGS4.000000-
DOCK_SOURCE_RINGS4.000000-
DOCK_SOURCE_RINGS4.000000-
DOCK_SOURCE_TPSA68.010000-
DOCK_SOURCE_TPSA68.010000-
DOCK_SOURCE_TPSA68.010000-
DOCK_STRAIN_DELTA37.115456-
DOCK_STRAIN_DELTA37.561891-
DOCK_STRAIN_DELTA31.576286-
DOCK_STRAIN_OK0-
DOCK_STRAIN_OK0-
DOCK_STRAIN_OK0-
DOCK_TARGETT01-
DOCK_TARGETT02-
DOCK_TARGETT16-
EXACT_MASS383.056232288Da
FORMULAC19H14FN3OS2-
HBA6-
HBD2-
LOGP5.0188000000000015-
MOL_WEIGHT383.47300000000007g/mol
QED_SCORE0.4857187140038478-
ROTATABLE_BONDS4-
TPSA68.01A^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
 0.9094118158195158 -27.4673 10 0.48 - Best pose
T02 T02 selection_import_t02 1
native pose available
 1.0185294571365404 -27.3748 10 0.48 - Best pose
T16 T16 selection_import_t16 1
native pose available
 1.504258611655206 -24.3892 6 0.50 - 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
571 0.9094118158195158 -1.01549 -27.4673 4 13 10 0.48 0.00 0.20 0.20 - no geometry warning; 8 clashes; 6 protein contact clashes; high strain Δ 37.1 Open pose
T02 — T02 1 poses · report selection_import_t02
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
560 1.0185294571365404 -1.01104 -27.3748 4 13 10 0.48 0.00 0.20 0.20 - no geometry warning; 9 clashes; 6 protein contact clashes; high strain Δ 37.6 Open pose
T16 — T16 1 poses · report selection_import_t16
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
568 1.504258611655206 -0.923793 -24.3892 5 15 6 0.50 - - - - no geometry warning; 8 clashes; 9 protein contact clashes; high strain Δ 31.6 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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