FAIRMol

Z56863482

ID 497

DB Docking_panel_21This detail page is pinned to the current database context.
Back to results Open docking pose (2)
2D structure

SMILES: Cc1ccc(NC(=O)c2sc3nc4c(c(-c5cccs5)c3c2N)CCCCC4)cc1

Formula: C24H23N3OS2 | MW: 433.6020000000003

LogP: 6.436620000000003 | TPSA: 68.01

HBA/HBD: 5/2 | RotB: 3

InChIKey: WJSKBGHZENYNGA-UHFFFAOYSA-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) H-bond acceptor N H-bond acceptor O H-bond donor ×2 Gatekeeper aromatic Ionizable base Metal chelator

Functional group

Carbonyl Amide Primary amine Secondary amine

Ring system

Benzene Pyridine Thiophene ×2
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Properties

NameValueUnit
DOCK_BASE_INTER_RANK-0.839901-
DOCK_BASE_INTER_RANK-0.677458-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_CLASH_COUNT8.000000-
DOCK_CLASH_COUNT10.000000-
DOCK_CONTACT_COUNT18.000000-
DOCK_CONTACT_COUNT10.000000-
DOCK_EXPERIMENTT03-
DOCK_EXPERIMENTT18-
DOCK_EXPERIMENT_ID2-
DOCK_EXPERIMENT_ID16-
DOCK_FINAL_RANK3.452849-
DOCK_FINAL_RANK4.147144-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOM_OK0-
DOCK_GEOM_OK0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_IFP::A:ALA321-
DOCK_IFP::A:ARG971-
DOCK_IFP::A:ASP1161-
DOCK_IFP::A:ASP521-
DOCK_IFP::A:GLU181-
DOCK_IFP::A:GLY1121-
DOCK_IFP::A:ILE1061-
DOCK_IFP::A:ILE451-
DOCK_IFP::A:LEU171-
DOCK_IFP::A:LEU941-
DOCK_IFP::A:LYS1081-
DOCK_IFP::A:LYS571-
DOCK_IFP::A:LYS951-
DOCK_IFP::A:MET1131-
DOCK_IFP::A:MET531-
DOCK_IFP::A:NDP3011-
DOCK_IFP::A:PHE561-
DOCK_IFP::A:PHE911-
DOCK_IFP::A:SER1091-
DOCK_IFP::A:SER861-
DOCK_IFP::A:THR831-
DOCK_IFP::A:TRP211-
DOCK_IFP::A:TYR1101-
DOCK_IFP::A:TYR1621-
DOCK_IFP::A:VAL1561-
DOCK_IFP::A:VAL301-
DOCK_IFP::A:VAL311-
DOCK_IFP::A:VAL871-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_MAX_CLASH_OVERLAP0.655170-
DOCK_MAX_CLASH_OVERLAP0.655229-
DOCK_POSE_COUNT1-
DOCK_POSE_COUNT1-
DOCK_PRE_RANK2.193199-
DOCK_PRE_RANK3.841418-
DOCK_PRIMARY_POSE_ID6462-
DOCK_PRIMARY_POSE_ID44620-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_REPORT_IDdockmulti_91311c650f2e_T03-
DOCK_REPORT_IDdockmulti_91311c650f2e_T18-
DOCK_RESIDUE_CONTACTSA:ALA32;A:ARG97;A:ASP52;A:ILE45;A:LEU94;A:LYS57;A:LYS95;A:MET53;A:NDP301;A:PHE56;A:PHE91;A:SER86;A:THR83;A:TYR162;A:VAL156;A:VAL30;A:VAL31;A:VAL87-
DOCK_RESIDUE_CONTACTSA:ASP116;A:GLU18;A:GLY112;A:ILE106;A:LEU17;A:LYS108;A:MET113;A:SER109;A:TRP21;A:TYR110-
DOCK_SCAFFOLDO=C(Nc1ccccc1)c1cc2c(-c3cccs3)c3c(nc2s1)CCCCC3-
DOCK_SCAFFOLDO=C(Nc1ccccc1)c1cc2c(-c3cccs3)c3c(nc2s1)CCCCC3-
DOCK_SCORE-16.940100-
DOCK_SCORE-18.501500-
DOCK_SCORE_INTER-25.197000-
DOCK_SCORE_INTER-20.323800-
DOCK_SCORE_INTER_KCAL-6.018203-
DOCK_SCORE_INTER_KCAL-4.854258-
DOCK_SCORE_INTER_NORM-0.839901-
DOCK_SCORE_INTER_NORM-0.677458-
DOCK_SCORE_INTRA8.256930-
DOCK_SCORE_INTRA1.822280-
DOCK_SCORE_INTRA_KCAL1.972135-
DOCK_SCORE_INTRA_KCAL0.435244-
DOCK_SCORE_INTRA_NORM0.275231-
DOCK_SCORE_INTRA_NORM0.060743-
DOCK_SCORE_KCAL-4.046075-
DOCK_SCORE_KCAL-4.419009-
DOCK_SCORE_NORM-0.564670-
DOCK_SCORE_NORM-0.616716-
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_FILEresults_T03_top1000.sdf-
DOCK_SOURCE_FILEresults_T18_top1000.sdf-
DOCK_SOURCE_FORMULAC24H23N3OS2-
DOCK_SOURCE_FORMULAC24H23N3OS2-
DOCK_SOURCE_HBA5.000000-
DOCK_SOURCE_HBA5.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HEAVY_ATOMS30.000000-
DOCK_SOURCE_HEAVY_ATOMS30.000000-
DOCK_SOURCE_LOGP6.436620-
DOCK_SOURCE_LOGP6.436620-
DOCK_SOURCE_MW433.602000-
DOCK_SOURCE_MW433.602000-
DOCK_SOURCE_NAMEZ56863482-
DOCK_SOURCE_NAMEZ56863482-
DOCK_SOURCE_RINGS5.000000-
DOCK_SOURCE_RINGS5.000000-
DOCK_SOURCE_TPSA68.010000-
DOCK_SOURCE_TPSA68.010000-
DOCK_STRAIN_DELTA32.994165-
DOCK_STRAIN_DELTA17.095435-
DOCK_STRAIN_OK0-
DOCK_STRAIN_OK0-
DOCK_TARGETT03-
DOCK_TARGETT18-
EXACT_MASS433.128254356Da
FORMULAC24H23N3OS2-
HBA5-
HBD2-
LOGP6.436620000000003-
MOL_WEIGHT433.6020000000003g/mol
QED_SCORE0.3655058628149928-
ROTATABLE_BONDS3-
TPSA68.01A^2

Samples

BatchAmountPurityState

Containers

NameLocationQR

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
T03 T03 dockmulti_91311c650f2e_T03 1
native pose available
 3.452848587962331 -16.9401 17 0.85 - Best pose
T18 T18 dockmulti_91311c650f2e_T18 1
native pose available
 4.147143649329101 -18.5015 9 0.69 - Best pose
T03 — T03 1 poses · report dockmulti_91311c650f2e_T03
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
3144 3.452848587962331 -0.839901 -16.9401 0 18 17 0.85 0.00 0.00 0.00 - no geometry warning; 8 clashes; 4 protein contact clashes; high strain Δ 33.0 Open pose
T18 — T18 1 poses · report dockmulti_91311c650f2e_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
2533 4.147143649329101 -0.677458 -18.5015 4 10 9 0.69 - - - - no geometry warning; 10 clashes; 7 protein contact clashes; moderate strain Δ 17.1 Open pose

Heterocycles & Functional Groups

Analysis powered by faircheckmol_nodb — click any item to highlight its atoms in the structure.
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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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⚗ AI Structural Analysis

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