FAIRMol

Z49596752

ID 2017

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

SMILES: C/C(=N/NC(=O)c1cccc(S(=O)(=O)N2CCOCC2)c1)c1cc(Cl)ccc1Cl

Formula: C19H19Cl2N3O4S | MW: 456.3510000000003

LogP: 3.1683000000000012 | TPSA: 88.07

HBA/HBD: 5/1 | RotB: 5

InChIKey: AUBKZBOZKIREHF-XKZIYDEJSA-N

Recognized patterns

Click a named motif to highlight it in the 2D depiction or launch reverse search.

Bio motif

Hinge binder (C=O-NH) Hinge binder (NH-C=O) Sulfonamide bioisostere H-bond acceptor N ×2 H-bond acceptor O ×4 H-bond donor Gatekeeper aromatic ×2 Metal chelator

Functional group

Carbonyl Amide Sulfonamide Chlorine ×2 Imine Ether

Ring system

Benzene ×2

Properties

NameValueUnit
DOCK_BASE_INTER_RANK-0.969320-
DOCK_BASE_INTER_RANK-0.856440-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_CLASH_COUNT11.000000-
DOCK_CLASH_COUNT12.000000-
DOCK_CONTACT_COUNT14.000000-
DOCK_CONTACT_COUNT14.000000-
DOCK_EXPERIMENTT10-
DOCK_EXPERIMENTT05-
DOCK_EXPERIMENT_ID10-
DOCK_EXPERIMENT_ID5-
DOCK_FINAL_RANK4.151662-
DOCK_FINAL_RANK1.222491-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOM_OK0-
DOCK_GEOM_OK0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_IFP::A:ALA151-
DOCK_IFP::A:ARG1161-
DOCK_IFP::A:ARG1401-
DOCK_IFP::A:ARG1441-
DOCK_IFP::A:ARG171-
DOCK_IFP::A:ASN1061-
DOCK_IFP::A:ASP131-
DOCK_IFP::A:ASP1811-
DOCK_IFP::A:CYS721-
DOCK_IFP::A:GLY2251-
DOCK_IFP::A:GLY731-
DOCK_IFP::A:GLY771-
DOCK_IFP::A:HIS1051-
DOCK_IFP::A:HIS141-
DOCK_IFP::A:HIS1411-
DOCK_IFP::A:HIS2411-
DOCK_IFP::A:LEU1881-
DOCK_IFP::A:LEU2261-
DOCK_IFP::A:LEU2291-
DOCK_IFP::A:MET1831-
DOCK_IFP::A:NDP3021-
DOCK_IFP::A:PHE1131-
DOCK_IFP::A:SER2271-
DOCK_IFP::A:THR741-
DOCK_IFP::A:TYR1941-
DOCK_IFP::A:TYR491-
DOCK_IFP::A:VAL2301-
DOCK_IFP::D:ARG2871-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_MAX_CLASH_OVERLAP0.620452-
DOCK_MAX_CLASH_OVERLAP0.618763-
DOCK_POSE_COUNT1-
DOCK_POSE_COUNT1-
DOCK_PRE_RANK4.107687-
DOCK_PRE_RANK1.203143-
DOCK_PRIMARY_POSE_ID3220-
DOCK_PRIMARY_POSE_ID6622-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_REPORT_IDselection_import_t05-
DOCK_REPORT_IDselection_import_t10-
DOCK_RESIDUE_CONTACTSA:ARG17;A:ASP181;A:GLY225;A:HIS241;A:LEU188;A:LEU226;A:LEU229;A:MET183;A:NDP302;A:PHE113;A:SER227;A:TYR194;A:VAL230;D:ARG287-
DOCK_RESIDUE_CONTACTSA:ALA15;A:ARG116;A:ARG140;A:ARG144;A:ASN106;A:ASP13;A:CYS72;A:GLY73;A:GLY77;A:HIS105;A:HIS14;A:HIS141;A:THR74;A:TYR49-
DOCK_SCAFFOLDO=C(NN=Cc1ccccc1)c1cccc(S(=O)(=O)N2CCOCC2)c1-
DOCK_SCAFFOLDO=S(=O)(c1cccc(C=NN=Cc2ccccc2)c1)N1CCOCC1-
DOCK_SCORE-27.474600-
DOCK_SCORE-26.022500-
DOCK_SCORE_INTER-28.110300-
DOCK_SCORE_INTER-24.836800-
DOCK_SCORE_INTER_KCAL-6.714033-
DOCK_SCORE_INTER_KCAL-5.932170-
DOCK_SCORE_INTER_NORM-0.856440-
DOCK_SCORE_INTER_NORM-0.969320-
DOCK_SCORE_INTRA-2.637840-
DOCK_SCORE_INTRA2.087750-
DOCK_SCORE_INTRA_KCAL0.498651-
DOCK_SCORE_INTRA_KCAL-0.630038-
DOCK_SCORE_INTRA_NORM-0.090960-
DOCK_SCORE_INTRA_NORM0.071991-
DOCK_SCORE_KCAL-6.215370-
DOCK_SCORE_KCAL-6.562198-
DOCK_SCORE_NORM-0.897328-
DOCK_SCORE_NORM-0.947400-
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_FILET10_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FILET05_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FORMULAC19H19Cl2N3O4S-
DOCK_SOURCE_FORMULAC19H19Cl2N3O4S-
DOCK_SOURCE_HBA5.000000-
DOCK_SOURCE_HBA5.000000-
DOCK_SOURCE_HBD1.000000-
DOCK_SOURCE_HBD1.000000-
DOCK_SOURCE_HEAVY_ATOMS29.000000-
DOCK_SOURCE_HEAVY_ATOMS29.000000-
DOCK_SOURCE_LOGP3.743100-
DOCK_SOURCE_LOGP3.168300-
DOCK_SOURCE_MW456.351000-
DOCK_SOURCE_MW456.351000-
DOCK_SOURCE_NAMEZ49596752-
DOCK_SOURCE_NAMEZ49596752-
DOCK_SOURCE_RINGS3.000000-
DOCK_SOURCE_RINGS3.000000-
DOCK_SOURCE_TPSA91.560000-
DOCK_SOURCE_TPSA88.070000-
DOCK_STRAIN_DELTA31.719753-
DOCK_STRAIN_DELTA15.353478-
DOCK_STRAIN_OK0-
DOCK_STRAIN_OK1-
DOCK_TARGETT10-
DOCK_TARGETT05-
EXACT_MASS455.04733244799996Da
FORMULAC19H19Cl2N3O4S-
HBA5-
HBD1-
LOGP3.1683000000000012-
MOL_WEIGHT456.3510000000003g/mol
QED_SCORE0.5532397921150921-
ROTATABLE_BONDS5-
TPSA88.07A^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
 1.2224907479128713 -26.0225 12 0.71 - Best pose
T10 T10 selection_import_t10 1
native pose available
 4.15166166876751 -27.4746 14 0.82 - 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
510 1.2224907479128713 -0.96932 -26.0225 8 14 12 0.71 0.29 0.33 0.40 - no geometry warning; 12 clashes; 5 protein contact clashes; 1 severe cofactor-context clash Open pose
T10 — T10 1 poses · report selection_import_t10
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
526 4.15166166876751 -0.85644 -27.4746 9 14 14 0.82 0.54 0.45 0.45 - no geometry warning; 11 clashes; 2 protein clashes; high strain Δ 31.7 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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