FAIRMol

Z20224548

ID 1876

DB Docking_panel_21This detail page is pinned to the current database context.
Back to results Open docking pose (3)
2D structure

SMILES: NC(=O)NC(=O)CSc1nc2sc(-c3ccccc3)cc2c(=O)n1-c1ccccc1

Formula: C21H16N4O3S2 | MW: 436.51800000000014

LogP: 3.401200000000002 | TPSA: 107.08000000000001

HBA/HBD: 6/2 | RotB: 5

InChIKey: JQZNBXVMRJATGE-UHFFFAOYSA-N

Recognized patterns

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

Bio motif

ATP mimic pyrimidine Hinge binder (C=O-NH) ×2 Hinge binder (NH-C=O) ×2 H-bond acceptor N ×2 H-bond acceptor O ×3 H-bond donor ×2 Gatekeeper aromatic ×2 Metal chelator ×3

Functional group

Carbonyl ×2 Amide ×3 Primary amine Secondary amine Urea Imide Sulfide

Ring system

Benzene ×2 Pyrimidine Thiophene
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Properties

NameValueUnit
DOCK_BASE_INTER_RANK-0.814210-
DOCK_BASE_INTER_RANK-0.685753-
DOCK_BASE_INTER_RANK-0.622403-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_CLASH_COUNT14.000000-
DOCK_CLASH_COUNT11.000000-
DOCK_CLASH_COUNT15.000000-
DOCK_CONTACT_COUNT18.000000-
DOCK_CONTACT_COUNT10.000000-
DOCK_CONTACT_COUNT12.000000-
DOCK_EXPERIMENTT09-
DOCK_EXPERIMENTT18-
DOCK_EXPERIMENTT20-
DOCK_EXPERIMENT_ID7-
DOCK_EXPERIMENT_ID16-
DOCK_EXPERIMENT_ID18-
DOCK_FINAL_RANK4.171771-
DOCK_FINAL_RANK3.630991-
DOCK_FINAL_RANK4.428069-
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:ASN4021-
DOCK_IFP::A:ASP1161-
DOCK_IFP::A:GLU1181-
DOCK_IFP::A:GLU181-
DOCK_IFP::A:GLU4661-
DOCK_IFP::A:GLU4671-
DOCK_IFP::A:GLY1121-
DOCK_IFP::A:LEU171-
DOCK_IFP::A:LEU3991-
DOCK_IFP::A:MET1131-
DOCK_IFP::A:MET4711-
DOCK_IFP::A:NDP3011-
DOCK_IFP::A:PHE3961-
DOCK_IFP::A:PRO3981-
DOCK_IFP::A:SER1091-
DOCK_IFP::A:SER3941-
DOCK_IFP::A:SER4641-
DOCK_IFP::A:SER4701-
DOCK_IFP::A:THR1171-
DOCK_IFP::A:THR3971-
DOCK_IFP::A:THR4631-
DOCK_IFP::A:TRP211-
DOCK_IFP::A:TYR1101-
DOCK_IFP::B:ALA321-
DOCK_IFP::B:ARG971-
DOCK_IFP::B:GLY1571-
DOCK_IFP::B:ILE451-
DOCK_IFP::B:LEU941-
DOCK_IFP::B:LYS571-
DOCK_IFP::B:MET531-
DOCK_IFP::B:PHE561-
DOCK_IFP::B:PHE911-
DOCK_IFP::B:PRO881-
DOCK_IFP::B:SER861-
DOCK_IFP::B:THR831-
DOCK_IFP::B:TYR1621-
DOCK_IFP::B:VAL1561-
DOCK_IFP::B:VAL301-
DOCK_IFP::B:VAL311-
DOCK_IFP::B:VAL871-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_MAX_CLASH_OVERLAP0.648809-
DOCK_MAX_CLASH_OVERLAP0.648838-
DOCK_MAX_CLASH_OVERLAP0.648845-
DOCK_POSE_COUNT1-
DOCK_POSE_COUNT1-
DOCK_POSE_COUNT1-
DOCK_PRE_RANK3.867265-
DOCK_PRE_RANK2.895069-
DOCK_PRE_RANK4.208911-
DOCK_PRIMARY_POSE_ID17175-
DOCK_PRIMARY_POSE_ID44269-
DOCK_PRIMARY_POSE_ID49249-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_REPORT_IDdockmulti_91311c650f2e_T09-
DOCK_REPORT_IDdockmulti_91311c650f2e_T18-
DOCK_REPORT_IDdockmulti_91311c650f2e_T20-
DOCK_RESIDUE_CONTACTSA:NDP301;B:ALA32;B:ARG97;B:GLY157;B:ILE45;B:LEU94;B:LYS57;B:MET53;B:PHE56;B:PHE91;B:PRO88;B:SER86;B:THR83;B:TYR162;B:VAL156;B:VAL30;B:VAL31;B:VAL87-
DOCK_RESIDUE_CONTACTSA:ASP116;A:GLU118;A:GLU18;A:GLY112;A:LEU17;A:MET113;A:SER109;A:THR117;A:TRP21;A:TYR110-
DOCK_RESIDUE_CONTACTSA:ASN402;A:GLU466;A:GLU467;A:LEU399;A:MET471;A:PHE396;A:PRO398;A:SER394;A:SER464;A:SER470;A:THR397;A:THR463-
DOCK_SCAFFOLDO=c1c2cc(-c3ccccc3)sc2ncn1-c1ccccc1-
DOCK_SCAFFOLDO=c1c2cc(-c3ccccc3)sc2ncn1-c1ccccc1-
DOCK_SCAFFOLDO=c1c2cc(-c3ccccc3)sc2ncn1-c1ccccc1-
DOCK_SCORE-24.294700-
DOCK_SCORE-18.935400-
DOCK_SCORE-15.530300-
DOCK_SCORE_INTER-24.426300-
DOCK_SCORE_INTER-20.572600-
DOCK_SCORE_INTER-18.672100-
DOCK_SCORE_INTER_KCAL-5.834124-
DOCK_SCORE_INTER_KCAL-4.913683-
DOCK_SCORE_INTER_KCAL-4.459756-
DOCK_SCORE_INTER_NORM-0.814210-
DOCK_SCORE_INTER_NORM-0.685753-
DOCK_SCORE_INTER_NORM-0.622403-
DOCK_SCORE_INTRA0.131602-
DOCK_SCORE_INTRA1.637190-
DOCK_SCORE_INTRA3.141800-
DOCK_SCORE_INTRA_KCAL0.031433-
DOCK_SCORE_INTRA_KCAL0.391036-
DOCK_SCORE_INTRA_KCAL0.750406-
DOCK_SCORE_INTRA_NORM0.004387-
DOCK_SCORE_INTRA_NORM0.054573-
DOCK_SCORE_INTRA_NORM0.104727-
DOCK_SCORE_KCAL-5.802692-
DOCK_SCORE_KCAL-4.522645-
DOCK_SCORE_KCAL-3.709350-
DOCK_SCORE_NORM-0.809823-
DOCK_SCORE_NORM-0.631180-
DOCK_SCORE_NORM-0.517677-
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_FILEresults_T09_top1000.sdf-
DOCK_SOURCE_FILEresults_T18_top1000.sdf-
DOCK_SOURCE_FILEresults_T20_top1000.sdf-
DOCK_SOURCE_FORMULAC21H16N4O3S2-
DOCK_SOURCE_FORMULAC21H16N4O3S2-
DOCK_SOURCE_FORMULAC21H16N4O3S2-
DOCK_SOURCE_HBA6.000000-
DOCK_SOURCE_HBA6.000000-
DOCK_SOURCE_HBA6.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HEAVY_ATOMS30.000000-
DOCK_SOURCE_HEAVY_ATOMS30.000000-
DOCK_SOURCE_HEAVY_ATOMS30.000000-
DOCK_SOURCE_LOGP3.401200-
DOCK_SOURCE_LOGP3.401200-
DOCK_SOURCE_LOGP3.401200-
DOCK_SOURCE_MW436.518000-
DOCK_SOURCE_MW436.518000-
DOCK_SOURCE_MW436.518000-
DOCK_SOURCE_NAMEZ20224548-
DOCK_SOURCE_NAMEZ20224548-
DOCK_SOURCE_NAMEZ20224548-
DOCK_SOURCE_RINGS4.000000-
DOCK_SOURCE_RINGS4.000000-
DOCK_SOURCE_RINGS4.000000-
DOCK_SOURCE_TPSA107.080000-
DOCK_SOURCE_TPSA107.080000-
DOCK_SOURCE_TPSA107.080000-
DOCK_STRAIN_DELTA17.075103-
DOCK_STRAIN_DELTA24.265366-
DOCK_STRAIN_DELTA15.652631-
DOCK_STRAIN_OK0-
DOCK_STRAIN_OK0-
DOCK_STRAIN_OK0-
DOCK_TARGETT09-
DOCK_TARGETT18-
DOCK_TARGETT20-
EXACT_MASS436.066382372Da
FORMULAC21H16N4O3S2-
HBA6-
HBD2-
LOGP3.401200000000002-
MOL_WEIGHT436.51800000000014g/mol
QED_SCORE0.3683028170976651-
ROTATABLE_BONDS5-
TPSA107.08000000000001A^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
T18 T18 dockmulti_91311c650f2e_T18 1
native pose available
 3.6309906069339783 -18.9354 9 0.69 - Best pose
T09 T09 dockmulti_91311c650f2e_T09 1
native pose available
 4.171771401974022 -24.2947 18 0.86 - Best pose
T20 T20 dockmulti_91311c650f2e_T20 1
native pose available
 4.428068810468293 -15.5303 8 1.00 - Best 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
2182 3.6309906069339783 -0.685753 -18.9354 4 10 9 0.69 - - - - no geometry warning; 11 clashes; 4 protein contact clashes; high strain Δ 24.3 Open pose
T09 — T09 1 poses · report dockmulti_91311c650f2e_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
1978 4.171771401974022 -0.81421 -24.2947 4 18 18 0.86 0.43 0.50 0.50 - no geometry warning; 14 clashes; 6 protein contact clashes; moderate strain Δ 17.1 Open pose
T20 — T20 1 poses · report dockmulti_91311c650f2e_T20
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
2284 4.428068810468293 -0.622403 -15.5303 6 12 8 1.00 0.50 1.00 1.00 - no geometry warning; 15 clashes; 5 protein contact clashes; moderate strain Δ 15.7 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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