FAIRMol

Z226983036

ID 3253

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

SMILES: Cc1nc2c3ccccc3nc(SCC(=O)c3ccc(Cl)c(Cl)c3)n2n1

Formula: C18H12Cl2N4OS | MW: 403.294

LogP: 4.867720000000002 | TPSA: 60.150000000000006

HBA/HBD: 5/- | RotB: 4

InChIKey: GSNZRAZHRXUNIK-UHFFFAOYSA-N

Recognized patterns

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

Bio motif

ATP mimic pyrimidine H-bond acceptor N ×4 H-bond acceptor O Gatekeeper aromatic ×2

Functional group

Carbonyl Ketone Chlorine ×2 Sulfide

Ring system

Benzene ×2 Pyrimidine

Properties

NameValueUnit
DOCK_BASE_INTER_RANK-1.008020-
DOCK_BASE_INTER_RANK-1.217560-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_CLASH_COUNT9.000000-
DOCK_CLASH_COUNT10.000000-
DOCK_CONTACT_COUNT15.000000-
DOCK_CONTACT_COUNT20.000000-
DOCK_EXPERIMENTT09-
DOCK_EXPERIMENTT19-
DOCK_EXPERIMENT_ID9-
DOCK_EXPERIMENT_ID19-
DOCK_FINAL_RANK2.003553-
DOCK_FINAL_RANK1.605796-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOM_OK0-
DOCK_GEOM_OK0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_IFP::A:NDP3011-
DOCK_IFP::B:ALA321-
DOCK_IFP::B:ARG481-
DOCK_IFP::B:ASP521-
DOCK_IFP::B:ILE451-
DOCK_IFP::B:MET531-
DOCK_IFP::B:PHE551-
DOCK_IFP::B:PHE561-
DOCK_IFP::B:SER441-
DOCK_IFP::B:THR1801-
DOCK_IFP::B:TRP471-
DOCK_IFP::B:VAL1561-
DOCK_IFP::B:VAL301-
DOCK_IFP::B:VAL311-
DOCK_IFP::B:VAL491-
DOCK_IFP::C:ALA3631-
DOCK_IFP::C:ALA3651-
DOCK_IFP::C:ARG2871-
DOCK_IFP::C:ASP3271-
DOCK_IFP::C:CYS571-
DOCK_IFP::C:GLY561-
DOCK_IFP::C:ILE1991-
DOCK_IFP::C:LEU3341-
DOCK_IFP::C:LYS601-
DOCK_IFP::C:MET3331-
DOCK_IFP::C:NDP8001-
DOCK_IFP::C:PHE1821-
DOCK_IFP::C:PHE2031-
DOCK_IFP::C:PHE3671-
DOCK_IFP::C:PRO3361-
DOCK_IFP::C:SER1781-
DOCK_IFP::C:SER3641-
DOCK_IFP::C:THR3351-
DOCK_IFP::C:THR511-
DOCK_IFP::C:VAL551-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_MAX_CLASH_OVERLAP0.615648-
DOCK_MAX_CLASH_OVERLAP0.615705-
DOCK_POSE_COUNT1-
DOCK_POSE_COUNT1-
DOCK_PRE_RANK1.981257-
DOCK_PRE_RANK1.587190-
DOCK_PRIMARY_POSE_ID5868-
DOCK_PRIMARY_POSE_ID12612-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_REPORT_IDselection_import_t09-
DOCK_REPORT_IDselection_import_t19-
DOCK_RESIDUE_CONTACTSA:NDP301;B:ALA32;B:ARG48;B:ASP52;B:ILE45;B:MET53;B:PHE55;B:PHE56;B:SER44;B:THR180;B:TRP47;B:VAL156;B:VAL30;B:VAL31;B:VAL49-
DOCK_RESIDUE_CONTACTSC:ALA363;C:ALA365;C:ARG287;C:ASP327;C:CYS57;C:GLY56;C:ILE199;C:LEU334;C:LYS60;C:MET333;C:NDP800;C:PHE182;C:PHE203;C:PHE367;C:PRO336;C:SER178;C:SER364;C:THR335;C:THR51;C:VAL55-
DOCK_SCAFFOLDO=C(CSc1nc2ccccc2c2ncnn12)c1ccccc1-
DOCK_SCAFFOLDO=C(CSc1nc2ccccc2c2ncnn12)c1ccccc1-
DOCK_SCORE-24.831900-
DOCK_SCORE-29.157200-
DOCK_SCORE_INTER-26.208600-
DOCK_SCORE_INTER-31.656400-
DOCK_SCORE_INTER_KCAL-6.259819-
DOCK_SCORE_INTER_KCAL-7.561005-
DOCK_SCORE_INTER_NORM-1.008020-
DOCK_SCORE_INTER_NORM-1.217560-
DOCK_SCORE_INTRA1.376660-
DOCK_SCORE_INTRA2.499280-
DOCK_SCORE_INTRA_KCAL0.328810-
DOCK_SCORE_INTRA_KCAL0.596943-
DOCK_SCORE_INTRA_NORM0.052949-
DOCK_SCORE_INTRA_NORM0.096126-
DOCK_SCORE_KCAL-5.931000-
DOCK_SCORE_KCAL-6.964081-
DOCK_SCORE_NORM-0.955075-
DOCK_SCORE_NORM-1.121430-
DOCK_SCORE_RESTR0.000000-
DOCK_SCORE_RESTR0.000000-
DOCK_SCORE_RESTR_NORM0.000000-
DOCK_SCORE_RESTR_NORM0.000000-
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_FILET09_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FILET19_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FORMULAC18H12Cl2N4OS-
DOCK_SOURCE_FORMULAC18H12Cl2N4OS-
DOCK_SOURCE_HBA5.000000-
DOCK_SOURCE_HBA5.000000-
DOCK_SOURCE_HBD0.000000-
DOCK_SOURCE_HBD0.000000-
DOCK_SOURCE_HEAVY_ATOMS26.000000-
DOCK_SOURCE_HEAVY_ATOMS26.000000-
DOCK_SOURCE_LOGP4.867720-
DOCK_SOURCE_LOGP4.867720-
DOCK_SOURCE_MW403.294000-
DOCK_SOURCE_MW403.294000-
DOCK_SOURCE_NAMEZ226983036-
DOCK_SOURCE_NAMEZ226983036-
DOCK_SOURCE_RINGS4.000000-
DOCK_SOURCE_RINGS4.000000-
DOCK_SOURCE_TPSA60.150000-
DOCK_SOURCE_TPSA60.150000-
DOCK_STRAIN_DELTA17.899970-
DOCK_STRAIN_DELTA14.666848-
DOCK_STRAIN_OK1-
DOCK_STRAIN_OK1-
DOCK_TARGETT09-
DOCK_TARGETT19-
EXACT_MASS402.01088736400004Da
FORMULAC18H12Cl2N4OS-
HBA5-
HBD0-
LOGP4.867720000000002-
MOL_WEIGHT403.294g/mol
QED_SCORE0.2765257673014241-
ROTATABLE_BONDS4-
TPSA60.150000000000006A^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
T19 T19 selection_import_t19 1
native pose available
 1.605795869295205 -29.1572 8 0.30 - Best pose
T09 T09 selection_import_t09 1
native pose available
 2.0035528962465103 -24.8319 11 0.52 - Best 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
411 1.605795869295205 -1.21756 -29.1572 5 20 8 0.30 0.08 0.20 0.25 - no geometry warning; 10 clashes; 1 protein clash; 2 cofactor-context clashes Open pose
T09 — T09 1 poses · report selection_import_t09
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
450 2.0035528962465103 -1.00802 -24.8319 2 15 11 0.52 0.00 0.00 0.00 - no geometry warning; 9 clashes; 1 protein clash 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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