FAIRMol

NMT-TY0977

ID 3188

DB SELECTIONThis detail page is pinned to the current database context.
Back to results Open docking pose (3)
2D structure

SMILES: CCCSc1nc(=O)c(NS(=O)(=O)c2ccccc2)c(N)[nH]1

Formula: C13H16N4O3S2 | MW: 340.4300000000001

LogP: 1.6550000000000002 | TPSA: 117.94

HBA/HBD: 6/3 | RotB: 6

InChIKey: MYIKRHWIEMNQFH-UHFFFAOYSA-N

Recognized patterns

Click a named motif to highlight it in the 2D depiction or launch reverse search.
Highlighted: 1 pattern H-bond acceptor N Clear highlight

Bio motif

ATP mimic pyrimidine Sulfonamide bioisostere H-bond acceptor N ×2 H-bond acceptor O ×3 H-bond donor ×3 Gatekeeper aromatic Ionizable base

Functional group

Primary amine Sulfonamide Sulfide

Ring system

Benzene Pyrimidine

Properties

NameValueUnit
DOCK_BASE_INTER_RANK-1.274170-
DOCK_BASE_INTER_RANK-1.100470-
DOCK_BASE_INTER_RANK-1.400340-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_CLASH_COUNT9.000000-
DOCK_CLASH_COUNT6.000000-
DOCK_CLASH_COUNT7.000000-
DOCK_CONTACT_COUNT14.000000-
DOCK_CONTACT_COUNT11.000000-
DOCK_CONTACT_COUNT19.000000-
DOCK_EXPERIMENTT09-
DOCK_EXPERIMENTT10-
DOCK_EXPERIMENTT22-
DOCK_EXPERIMENT_ID9-
DOCK_EXPERIMENT_ID10-
DOCK_EXPERIMENT_ID22-
DOCK_FINAL_RANK1.013997-
DOCK_FINAL_RANK4.170702-
DOCK_FINAL_RANK4.569153-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOM_OK0-
DOCK_GEOM_OK0-
DOCK_GEOM_OK0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_IFP::A:ALA151-
DOCK_IFP::A:ALA1581-
DOCK_IFP::A:ALA241-
DOCK_IFP::A:ALA701-
DOCK_IFP::A:ARG1161-
DOCK_IFP::A:ARG1401-
DOCK_IFP::A:ARG1441-
DOCK_IFP::A:ASN1261-
DOCK_IFP::A:ASP131-
DOCK_IFP::A:ASP681-
DOCK_IFP::A:CYS721-
DOCK_IFP::A:GLU731-
DOCK_IFP::A:GLY231-
DOCK_IFP::A:GLY251-
DOCK_IFP::A:GLY711-
DOCK_IFP::A:GLY731-
DOCK_IFP::A:HIS1051-
DOCK_IFP::A:HIS141-
DOCK_IFP::A:HIS1411-
DOCK_IFP::A:ILE291-
DOCK_IFP::A:LYS1271-
DOCK_IFP::A:LYS1591-
DOCK_IFP::A:LYS261-
DOCK_IFP::A:NDP3011-
DOCK_IFP::A:PHE381-
DOCK_IFP::A:SER221-
DOCK_IFP::A:SER271-
DOCK_IFP::A:SER281-
DOCK_IFP::A:SER461-
DOCK_IFP::A:THR441-
DOCK_IFP::A:THR691-
DOCK_IFP::B:ALA321-
DOCK_IFP::B:ARG481-
DOCK_IFP::B:ASP521-
DOCK_IFP::B:ILE1821-
DOCK_IFP::B:ILE451-
DOCK_IFP::B:MET531-
DOCK_IFP::B:PHE561-
DOCK_IFP::B:TRP471-
DOCK_IFP::B:TYR1621-
DOCK_IFP::B:VAL1561-
DOCK_IFP::B:VAL301-
DOCK_IFP::B:VAL311-
DOCK_IFP::B:VAL491-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_MAX_CLASH_OVERLAP0.635264-
DOCK_MAX_CLASH_OVERLAP0.660933-
DOCK_MAX_CLASH_OVERLAP0.649417-
DOCK_POSE_COUNT1-
DOCK_POSE_COUNT1-
DOCK_POSE_COUNT1-
DOCK_PRE_RANK0.957535-
DOCK_PRE_RANK4.125425-
DOCK_PRE_RANK4.518010-
DOCK_PRIMARY_POSE_ID5758-
DOCK_PRIMARY_POSE_ID6384-
DOCK_PRIMARY_POSE_ID14571-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_REPORT_IDselection_import_t09-
DOCK_REPORT_IDselection_import_t10-
DOCK_REPORT_IDselection_import_t22-
DOCK_RESIDUE_CONTACTSA:NDP301;B:ALA32;B:ARG48;B:ASP52;B:ILE182;B:ILE45;B:MET53;B:PHE56;B:TRP47;B:TYR162;B:VAL156;B:VAL30;B:VAL31;B:VAL49-
DOCK_RESIDUE_CONTACTSA:ALA15;A:ARG116;A:ARG140;A:ARG144;A:ASP13;A:CYS72;A:GLY73;A:HIS105;A:HIS14;A:HIS141;A:SER46-
DOCK_RESIDUE_CONTACTSA:ALA158;A:ALA24;A:ALA70;A:ASN126;A:ASP68;A:GLU73;A:GLY23;A:GLY25;A:GLY71;A:ILE29;A:LYS127;A:LYS159;A:LYS26;A:PHE38;A:SER22;A:SER27;A:SER28;A:THR44;A:THR69-
DOCK_SCAFFOLDO=c1nc[nH]cc1NS(=O)(=O)c1ccccc1-
DOCK_SCAFFOLDN=c1[nH]cncc1NS(=O)(=O)c1ccccc1-
DOCK_SCAFFOLDO=c1[nH]cncc1NS(=O)(=O)c1ccccc1-
DOCK_SCORE-26.695500-
DOCK_SCORE-25.073700-
DOCK_SCORE-29.508100-
DOCK_SCORE_INTER-28.031800-
DOCK_SCORE_INTER-24.210400-
DOCK_SCORE_INTER-30.807500-
DOCK_SCORE_INTER_KCAL-6.695283-
DOCK_SCORE_INTER_KCAL-5.782557-
DOCK_SCORE_INTER_KCAL-7.358248-
DOCK_SCORE_INTER_NORM-1.274170-
DOCK_SCORE_INTER_NORM-1.100470-
DOCK_SCORE_INTER_NORM-1.400340-
DOCK_SCORE_INTRA1.336300-
DOCK_SCORE_INTRA-0.863347-
DOCK_SCORE_INTRA1.299370-
DOCK_SCORE_INTRA_KCAL0.319170-
DOCK_SCORE_INTRA_KCAL-0.206207-
DOCK_SCORE_INTRA_KCAL0.310349-
DOCK_SCORE_INTRA_NORM0.060741-
DOCK_SCORE_INTRA_NORM-0.039243-
DOCK_SCORE_INTRA_NORM0.059062-
DOCK_SCORE_KCAL-6.376113-
DOCK_SCORE_KCAL-5.988753-
DOCK_SCORE_KCAL-7.047892-
DOCK_SCORE_NORM-1.213430-
DOCK_SCORE_NORM-1.139710-
DOCK_SCORE_NORM-1.341280-
DOCK_SCORE_RESTR0.000000-
DOCK_SCORE_RESTR0.000000-
DOCK_SCORE_RESTR0.000000-
DOCK_SCORE_RESTR_NORM0.000000-
DOCK_SCORE_RESTR_NORM0.000000-
DOCK_SCORE_RESTR_NORM0.000000-
DOCK_SCORE_SYSTEM0.000000-
DOCK_SCORE_SYSTEM0.000000-
DOCK_SCORE_SYSTEM0.000000-
DOCK_SCORE_SYSTEM_NORM0.000000-
DOCK_SCORE_SYSTEM_NORM0.000000-
DOCK_SCORE_SYSTEM_NORM0.000000-
DOCK_SELECTION_EXCLUDED0-
DOCK_SELECTION_EXCLUDED0-
DOCK_SELECTION_EXCLUDED0-
DOCK_SEVERE_CLASH_COUNT0.000000-
DOCK_SEVERE_CLASH_COUNT0.000000-
DOCK_SEVERE_CLASH_COUNT0.000000-
DOCK_SOURCE_FILET09_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FILET10_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FILET22_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FORMULAC13H16N4O3S2-
DOCK_SOURCE_FORMULAC13H16N4O3S2-
DOCK_SOURCE_FORMULAC13H16N4O3S2-
DOCK_SOURCE_HBA6.000000-
DOCK_SOURCE_HBA6.000000-
DOCK_SOURCE_HBA6.000000-
DOCK_SOURCE_HBD3.000000-
DOCK_SOURCE_HBD4.000000-
DOCK_SOURCE_HBD3.000000-
DOCK_SOURCE_HEAVY_ATOMS22.000000-
DOCK_SOURCE_HEAVY_ATOMS22.000000-
DOCK_SOURCE_HEAVY_ATOMS22.000000-
DOCK_SOURCE_LOGP1.655000-
DOCK_SOURCE_LOGP1.897670-
DOCK_SOURCE_LOGP1.655000-
DOCK_SOURCE_MW340.430000-
DOCK_SOURCE_MW340.430000-
DOCK_SOURCE_MW340.430000-
DOCK_SOURCE_NAMENMT-TY0977-
DOCK_SOURCE_NAMENMT-TY0977-
DOCK_SOURCE_NAMENMT-TY0977-
DOCK_SOURCE_RINGS2.000000-
DOCK_SOURCE_RINGS2.000000-
DOCK_SOURCE_RINGS2.000000-
DOCK_SOURCE_TPSA117.940000-
DOCK_SOURCE_TPSA118.930000-
DOCK_SOURCE_TPSA117.940000-
DOCK_STRAIN_DELTA37.850000-
DOCK_STRAIN_DELTA32.397858-
DOCK_STRAIN_DELTA35.331300-
DOCK_STRAIN_OK0-
DOCK_STRAIN_OK0-
DOCK_STRAIN_OK0-
DOCK_TARGETT09-
DOCK_TARGETT10-
DOCK_TARGETT22-
EXACT_MASS340.066382372Da
FORMULAC13H16N4O3S2-
HBA6-
HBD3-
LOGP1.6550000000000002-
MOL_WEIGHT340.4300000000001g/mol
QED_SCORE0.5434796675379806-
ROTATABLE_BONDS6-
TPSA117.94A^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
T09 T09 selection_import_t09 1
native pose available
 1.0139970207698543 -26.6955 10 0.48 - Best pose
T10 T10 selection_import_t10 1
native pose available
 4.170702248235619 -25.0737 10 0.59 - Best pose
T22 T22 selection_import_t22 1
native pose available
 4.569152508881392 -29.5081 13 0.62 - Best 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
340 1.0139970207698543 -1.27417 -26.6955 9 14 10 0.48 0.00 0.17 0.17 - no geometry warning; 9 clashes; 7 protein contact clashes; high strain Δ 37.9 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
288 4.170702248235619 -1.10047 -25.0737 12 11 10 0.59 0.23 0.18 0.27 - no geometry warning; 6 clashes; 3 protein clashes; high strain Δ 32.4 Open pose
T22 — T22 1 poses · report selection_import_t22
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
333 4.569152508881392 -1.40034 -29.5081 8 19 13 0.62 0.40 0.36 0.36 - no geometry warning; 7 clashes; 3 protein clashes; high strain Δ 35.3 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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