FAIRMol

Z45452525

ID 328

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

SMILES: CN(C)c1ccc([C@H](CNS(=O)(=O)c2ccc(F)c(F)c2)c2c[nH]c3ccccc23)cc1

Formula: C24H23F2N3O2S | MW: 455.53000000000014

LogP: 4.622500000000004 | TPSA: 65.2

HBA/HBD: 3/2 | RotB: 7

InChIKey: OMRUCSXLPQAINA-FQEVSTJZSA-N

Recognized patterns

Click a named motif to highlight it in the 2D depiction or launch reverse search.
Highlighted: 1 pattern P-gp efflux flag Clear highlight

Bio motif

Sulfonamide bioisostere H-bond acceptor N ×2 H-bond acceptor O ×2 H-bond donor ×2 Gatekeeper aromatic ×3 P-gp efflux flag

Functional group

Tertiary amine Sulfonamide Fluorine ×2

Ring system

Benzene ×3 Indole Pyrrole Isoindole

Properties

NameValueUnit
DOCK_BASE_INTER_RANK-0.802139-
DOCK_BASE_INTER_RANK-0.653259-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_CLASH_COUNT9.000000-
DOCK_CLASH_COUNT11.000000-
DOCK_CONTACT_COUNT18.000000-
DOCK_CONTACT_COUNT12.000000-
DOCK_EXPERIMENTT01-
DOCK_EXPERIMENTT18-
DOCK_EXPERIMENT_ID1-
DOCK_EXPERIMENT_ID18-
DOCK_FINAL_RANK1.997314-
DOCK_FINAL_RANK2.481260-
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:ASN651-
DOCK_IFP::A:ASP1161-
DOCK_IFP::A:GLU181-
DOCK_IFP::A:GLU311-
DOCK_IFP::A:ILE1061-
DOCK_IFP::A:ILE3391-
DOCK_IFP::A:ILE611-
DOCK_IFP::A:ILE81-
DOCK_IFP::A:LEU171-
DOCK_IFP::A:LEU231-
DOCK_IFP::A:LEU281-
DOCK_IFP::A:LEU681-
DOCK_IFP::A:MET1131-
DOCK_IFP::A:NAP2011-
DOCK_IFP::A:PHE321-
DOCK_IFP::A:PHE351-
DOCK_IFP::A:PRO271-
DOCK_IFP::A:PRO621-
DOCK_IFP::A:SER1091-
DOCK_IFP::A:SER141-
DOCK_IFP::A:THR1171-
DOCK_IFP::A:THR3351-
DOCK_IFP::A:THR571-
DOCK_IFP::A:TRP211-
DOCK_IFP::A:TRP251-
DOCK_IFP::A:TYR1101-
DOCK_IFP::A:TYR1221-
DOCK_IFP::A:VAL1161-
DOCK_IFP::A:VAL91-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_MAX_CLASH_OVERLAP0.635971-
DOCK_MAX_CLASH_OVERLAP0.675280-
DOCK_POSE_COUNT1-
DOCK_POSE_COUNT1-
DOCK_PRE_RANK1.938272-
DOCK_PRE_RANK2.426051-
DOCK_PRIMARY_POSE_ID493-
DOCK_PRIMARY_POSE_ID11985-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_REPORT_IDselection_import_t01-
DOCK_REPORT_IDselection_import_t18-
DOCK_RESIDUE_CONTACTSA:ALA10;A:ASN65;A:GLU31;A:ILE61;A:ILE8;A:LEU23;A:LEU28;A:LEU68;A:NAP201;A:PHE32;A:PHE35;A:PRO27;A:PRO62;A:THR57;A:TRP25;A:TYR122;A:VAL116;A:VAL9-
DOCK_RESIDUE_CONTACTSA:ASP116;A:GLU18;A:ILE106;A:ILE339;A:LEU17;A:MET113;A:SER109;A:SER14;A:THR117;A:THR335;A:TRP21;A:TYR110-
DOCK_SCAFFOLDO=S(=O)(NCC(c1ccccc1)c1c[nH]c2ccccc12)c1ccccc1-
DOCK_SCAFFOLDO=S(=O)(NCC(c1ccccc1)c1c[nH]c2ccccc12)c1ccccc1-
DOCK_SCORE-24.916200-
DOCK_SCORE-21.502900-
DOCK_SCORE_INTER-25.668500-
DOCK_SCORE_INTER-20.904300-
DOCK_SCORE_INTER_KCAL-6.130819-
DOCK_SCORE_INTER_KCAL-4.992908-
DOCK_SCORE_INTER_NORM-0.802139-
DOCK_SCORE_INTER_NORM-0.653259-
DOCK_SCORE_INTRA0.752302-
DOCK_SCORE_INTRA-0.598633-
DOCK_SCORE_INTRA_KCAL0.179684-
DOCK_SCORE_INTRA_KCAL-0.142981-
DOCK_SCORE_INTRA_NORM0.023509-
DOCK_SCORE_INTRA_NORM-0.018707-
DOCK_SCORE_KCAL-5.951135-
DOCK_SCORE_KCAL-5.135882-
DOCK_SCORE_NORM-0.778630-
DOCK_SCORE_NORM-0.671967-
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_FILET01_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FILET18_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FORMULAC24H23F2N3O2S-
DOCK_SOURCE_FORMULAC24H23F2N3O2S-
DOCK_SOURCE_HBA3.000000-
DOCK_SOURCE_HBA3.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HEAVY_ATOMS32.000000-
DOCK_SOURCE_HEAVY_ATOMS32.000000-
DOCK_SOURCE_LOGP4.622500-
DOCK_SOURCE_LOGP4.622500-
DOCK_SOURCE_MW455.530000-
DOCK_SOURCE_MW455.530000-
DOCK_SOURCE_NAMEZ45452525-
DOCK_SOURCE_NAMEZ45452525-
DOCK_SOURCE_RINGS4.000000-
DOCK_SOURCE_RINGS4.000000-
DOCK_SOURCE_TPSA65.200000-
DOCK_SOURCE_TPSA65.200000-
DOCK_STRAIN_DELTA39.032198-
DOCK_STRAIN_DELTA37.267015-
DOCK_STRAIN_OK0-
DOCK_STRAIN_OK0-
DOCK_TARGETT01-
DOCK_TARGETT18-
EXACT_MASS455.1479044160001Da
FORMULAC24H23F2N3O2S-
HBA3-
HBD2-
LOGP4.622500000000004-
MOL_WEIGHT455.53000000000014g/mol
QED_SCORE0.4273677703537986-
ROTATABLE_BONDS7-
TPSA65.2A^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
 1.9973139696583404 -24.9162 15 0.71 - Best pose
T18 T18 selection_import_t18 1
native pose available
 2.481260008237879 -21.5029 10 0.77 - 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
493 1.9973139696583404 -0.802139 -24.9162 2 18 15 0.71 0.40 0.40 0.40 - no geometry warning; 9 clashes; 1 protein clash; high strain Δ 39.0 Open pose
T18 — T18 1 poses · report selection_import_t18
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
464 2.481260008237879 -0.653259 -21.5029 1 12 10 0.77 - - - - no geometry warning; 11 clashes; 1 protein clash; high strain Δ 37.3 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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