FAIRMol

Z30217191

ID 3014

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

SMILES: C[C@@H]1CN(S(=O)(=O)c2ccc(C(=O)NCCCn3ccnc3)cc2)C[C@H](C)O1

Formula: C19H26N4O4S | MW: 406.50800000000015

LogP: 1.5010999999999994 | TPSA: 93.53

HBA/HBD: 5/1 | RotB: 7

InChIKey: XZRLCYJDDBDQPV-IYBDPMFKSA-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 ×3 H-bond acceptor O ×4 H-bond donor Gatekeeper aromatic Metal chelator

Functional group

Carbonyl Amide Secondary amine Sulfonamide Ether

Ring system

Benzene

Properties

NameValueUnit
DOCK_BASE_INTER_RANK-1.149260-
DOCK_BASE_INTER_RANK-1.003990-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_CLASH_COUNT7.000000-
DOCK_CLASH_COUNT7.000000-
DOCK_CONTACT_COUNT15.000000-
DOCK_CONTACT_COUNT16.000000-
DOCK_EXPERIMENTT08-
DOCK_EXPERIMENTT12-
DOCK_EXPERIMENT_ID8-
DOCK_EXPERIMENT_ID12-
DOCK_FINAL_RANK0.650138-
DOCK_FINAL_RANK4.498195-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOM_OK0-
DOCK_GEOM_OK0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_IFP::A:ARG141-
DOCK_IFP::A:ARG1401-
DOCK_IFP::A:ARG1441-
DOCK_IFP::A:ASN1061-
DOCK_IFP::A:ASN1751-
DOCK_IFP::A:ASP1611-
DOCK_IFP::A:CYS1681-
DOCK_IFP::A:HIS1051-
DOCK_IFP::A:HIS1411-
DOCK_IFP::A:LEU2081-
DOCK_IFP::A:LEU2091-
DOCK_IFP::A:MET1011-
DOCK_IFP::A:MET1631-
DOCK_IFP::A:NAP3011-
DOCK_IFP::A:PHE1711-
DOCK_IFP::A:PHE971-
DOCK_IFP::A:PRO1671-
DOCK_IFP::A:PRO2101-
DOCK_IFP::A:TYR1741-
DOCK_IFP::A:TYR971-
DOCK_IFP::A:TYR981-
DOCK_IFP::A:VAL1641-
DOCK_IFP::B:ARG1161-
DOCK_IFP::B:ARG461-
DOCK_IFP::B:CYS721-
DOCK_IFP::B:GLY731-
DOCK_IFP::B:GLY771-
DOCK_IFP::B:HIS141-
DOCK_IFP::B:ILE151-
DOCK_IFP::B:ILE761-
DOCK_IFP::B:SER741-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_MAX_CLASH_OVERLAP0.609291-
DOCK_MAX_CLASH_OVERLAP0.609217-
DOCK_POSE_COUNT1-
DOCK_POSE_COUNT1-
DOCK_PRE_RANK0.627141-
DOCK_PRE_RANK4.470659-
DOCK_PRIMARY_POSE_ID5200-
DOCK_PRIMARY_POSE_ID7894-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_REPORT_IDselection_import_t08-
DOCK_REPORT_IDselection_import_t12-
DOCK_RESIDUE_CONTACTSA:ARG14;A:ASN175;A:ASP161;A:CYS168;A:LEU208;A:LEU209;A:MET163;A:NAP301;A:PHE171;A:PHE97;A:PRO167;A:PRO210;A:TYR174;A:TYR98;A:VAL164-
DOCK_RESIDUE_CONTACTSA:ARG140;A:ARG144;A:ASN106;A:HIS105;A:HIS141;A:MET101;A:TYR97;B:ARG116;B:ARG46;B:CYS72;B:GLY73;B:GLY77;B:HIS14;B:ILE15;B:ILE76;B:SER74-
DOCK_SCAFFOLDO=C(NCCCn1ccnc1)c1ccc(S(=O)(=O)N2CCOCC2)cc1-
DOCK_SCAFFOLDO=C(NCCCn1ccnc1)c1ccc(S(=O)(=O)N2CCOCC2)cc1-
DOCK_SCORE-31.488600-
DOCK_SCORE-24.935000-
DOCK_SCORE_INTER-32.179200-
DOCK_SCORE_INTER-28.111600-
DOCK_SCORE_INTER_KCAL-7.685873-
DOCK_SCORE_INTER_KCAL-6.714343-
DOCK_SCORE_INTER_NORM-1.149260-
DOCK_SCORE_INTER_NORM-1.003990-
DOCK_SCORE_INTRA0.690671-
DOCK_SCORE_INTRA3.176690-
DOCK_SCORE_INTRA_KCAL0.164964-
DOCK_SCORE_INTRA_KCAL0.758740-
DOCK_SCORE_INTRA_NORM0.024667-
DOCK_SCORE_INTRA_NORM0.113453-
DOCK_SCORE_KCAL-7.520926-
DOCK_SCORE_KCAL-5.955625-
DOCK_SCORE_NORM-1.124590-
DOCK_SCORE_NORM-0.890534-
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_FILET08_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FILET12_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FORMULAC19H26N4O4S-
DOCK_SOURCE_FORMULAC19H26N4O4S-
DOCK_SOURCE_HBA5.000000-
DOCK_SOURCE_HBA5.000000-
DOCK_SOURCE_HBD1.000000-
DOCK_SOURCE_HBD1.000000-
DOCK_SOURCE_HEAVY_ATOMS28.000000-
DOCK_SOURCE_HEAVY_ATOMS28.000000-
DOCK_SOURCE_LOGP1.501100-
DOCK_SOURCE_LOGP1.501100-
DOCK_SOURCE_MW406.508000-
DOCK_SOURCE_MW406.508000-
DOCK_SOURCE_NAMEZ30217191-
DOCK_SOURCE_NAMEZ30217191-
DOCK_SOURCE_RINGS3.000000-
DOCK_SOURCE_RINGS3.000000-
DOCK_SOURCE_TPSA93.530000-
DOCK_SOURCE_TPSA93.530000-
DOCK_STRAIN_DELTA18.466786-
DOCK_STRAIN_DELTA21.867010-
DOCK_STRAIN_OK1-
DOCK_STRAIN_OK1-
DOCK_TARGETT08-
DOCK_TARGETT12-
EXACT_MASS406.16747631199996Da
FORMULAC19H26N4O4S-
HBA5-
HBD1-
LOGP1.5010999999999994-
MOL_WEIGHT406.50800000000015g/mol
QED_SCORE0.7036013737123858-
ROTATABLE_BONDS7-
TPSA93.53A^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
T08 T08 selection_import_t08 1
native pose available
 0.6501375225651361 -31.4886 11 0.58 - Best pose
T12 T12 selection_import_t12 1
native pose available
 4.498195063356032 -24.935 13 0.81 - Best pose
T08 — T08 1 poses · report selection_import_t08
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
459 0.6501375225651361 -1.14926 -31.4886 7 15 11 0.58 0.17 0.20 0.60 - no geometry warning; 7 clashes; 6 protein contact clashes; 3 cofactor-context clashes Open pose
T12 — T12 1 poses · report selection_import_t12
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
442 4.498195063356032 -1.00399 -24.935 11 16 13 0.81 0.67 0.80 0.80 - no geometry warning; 7 clashes; 3 protein clashes; moderate strain Δ 21.9 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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