FAIRMol

ulfkktlib_445

ID 3186

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

SMILES: O=C(NCc1cc(Cl)cc(Cl)c1)c1cn(Cc2ccccc2)n2c(=O)cc[nH+]c12

Formula: C21H17Cl2N4O2+ | MW: 428.29900000000015

LogP: 3.2002000000000015 | TPSA: 69.65

HBA/HBD: 2/1 | RotB: 5

InChIKey: RFCNDKZBWBNVPY-UHFFFAOYSA-O

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

Functional group

Carbonyl Amide Secondary amine Chlorine ×2

Ring system

Benzene ×2 Pyrimidine

Properties

NameValueUnit
DOCK_BASE_INTER_RANK-0.881401-
DOCK_BASE_INTER_RANK-0.882525-
DOCK_BASE_INTER_RANK-0.809682-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_CLASH_COUNT12.000000-
DOCK_CLASH_COUNT10.000000-
DOCK_CLASH_COUNT11.000000-
DOCK_CONTACT_COUNT19.000000-
DOCK_CONTACT_COUNT20.000000-
DOCK_CONTACT_COUNT16.000000-
DOCK_EXPERIMENTT09-
DOCK_EXPERIMENTT09-
DOCK_EXPERIMENTT17-
DOCK_EXPERIMENT_ID9-
DOCK_EXPERIMENT_ID9-
DOCK_EXPERIMENT_ID17-
DOCK_FINAL_RANK0.972930-
DOCK_FINAL_RANK1.103342-
DOCK_FINAL_RANK1.192980-
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:ALA2841-
DOCK_IFP::A:ARG2281-
DOCK_IFP::A:ARG2871-
DOCK_IFP::A:ARG3311-
DOCK_IFP::A:ASP3301-
DOCK_IFP::A:GLY1971-
DOCK_IFP::A:GLY2291-
DOCK_IFP::A:GLY2861-
DOCK_IFP::A:ILE1991-
DOCK_IFP::A:LEU3321-
DOCK_IFP::A:LEU3341-
DOCK_IFP::A:MET3331-
DOCK_IFP::A:NDP3011-
DOCK_IFP::A:NDP3011-
DOCK_IFP::A:PHE1981-
DOCK_IFP::A:PHE2301-
DOCK_IFP::A:SER2001-
DOCK_IFP::A:THR3741-
DOCK_IFP::B:ALA321-
DOCK_IFP::B:ALA321-
DOCK_IFP::B:ARG481-
DOCK_IFP::B:ARG481-
DOCK_IFP::B:ASP521-
DOCK_IFP::B:ASP521-
DOCK_IFP::B:ILE451-
DOCK_IFP::B:ILE451-
DOCK_IFP::B:LEU941-
DOCK_IFP::B:MET531-
DOCK_IFP::B:MET531-
DOCK_IFP::B:PHE561-
DOCK_IFP::B:PHE561-
DOCK_IFP::B:PHE911-
DOCK_IFP::B:PRO881-
DOCK_IFP::B:PRO881-
DOCK_IFP::B:SER441-
DOCK_IFP::B:SER861-
DOCK_IFP::B:SER861-
DOCK_IFP::B:THR1801-
DOCK_IFP::B:THR1801-
DOCK_IFP::B:THR831-
DOCK_IFP::B:THR831-
DOCK_IFP::B:TRP471-
DOCK_IFP::B:TRP471-
DOCK_IFP::B:TYR1621-
DOCK_IFP::B:TYR1621-
DOCK_IFP::B:VAL1561-
DOCK_IFP::B:VAL1561-
DOCK_IFP::B:VAL301-
DOCK_IFP::B:VAL301-
DOCK_IFP::B:VAL311-
DOCK_IFP::B:VAL311-
DOCK_IFP::B:VAL491-
DOCK_IFP::B:VAL491-
DOCK_IFP::B:VAL871-
DOCK_IFP::B:VAL871-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_MAX_CLASH_OVERLAP0.632481-
DOCK_MAX_CLASH_OVERLAP0.632449-
DOCK_MAX_CLASH_OVERLAP0.632483-
DOCK_POSE_COUNT2-
DOCK_POSE_COUNT1-
DOCK_PRE_RANK0.854711-
DOCK_PRE_RANK1.032645-
DOCK_PRE_RANK1.135833-
DOCK_PRIMARY_POSE_ID5604-
DOCK_PRIMARY_POSE_ID11051-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_REPORT_IDselection_import_t09-
DOCK_REPORT_IDselection_import_t09-
DOCK_REPORT_IDselection_import_t17-
DOCK_RESIDUE_CONTACTSA:NDP301;B:ALA32;B:ARG48;B:ASP52;B:ILE45;B:MET53;B:PHE56;B:PRO88;B:SER44;B:SER86;B:THR180;B:THR83;B:TRP47;B:TYR162;B:VAL156;B:VAL30;B:VAL31;B:VAL49;B:VAL87-
DOCK_RESIDUE_CONTACTSA:NDP301;B:ALA32;B:ARG48;B:ASP52;B:ILE45;B:LEU94;B:MET53;B:PHE56;B:PHE91;B:PRO88;B:SER86;B:THR180;B:THR83;B:TRP47;B:TYR162;B:VAL156;B:VAL30;B:VAL31;B:VAL49;B:VAL87-
DOCK_RESIDUE_CONTACTSA:ALA284;A:ARG228;A:ARG287;A:ARG331;A:ASP330;A:GLY197;A:GLY229;A:GLY286;A:ILE199;A:LEU332;A:LEU334;A:MET333;A:PHE198;A:PHE230;A:SER200;A:THR374-
DOCK_SCAFFOLDO=C(NCc1ccccc1)c1cn(Cc2ccccc2)n2c(=O)cc[nH+]c12-
DOCK_SCAFFOLDO=C(NCc1ccccc1)c1cn(Cc2ccccc2)n2c(=O)cc[nH+]c12-
DOCK_SCAFFOLDO=C(NCc1ccccc1)c1cn(Cc2ccccc2)n2c(=O)cc[nH+]c12-
DOCK_SCORE-22.289700-
DOCK_SCORE-21.951400-
DOCK_SCORE-21.507700-
DOCK_SCORE_INTER-25.560600-
DOCK_SCORE_INTER-25.593200-
DOCK_SCORE_INTER-23.480800-
DOCK_SCORE_INTER_KCAL-6.105047-
DOCK_SCORE_INTER_KCAL-6.112833-
DOCK_SCORE_INTER_KCAL-5.608295-
DOCK_SCORE_INTER_NORM-0.881401-
DOCK_SCORE_INTER_NORM-0.882525-
DOCK_SCORE_INTER_NORM-0.809682-
DOCK_SCORE_INTRA3.270950-
DOCK_SCORE_INTRA3.641810-
DOCK_SCORE_INTRA1.973120-
DOCK_SCORE_INTRA_KCAL0.781253-
DOCK_SCORE_INTRA_KCAL0.869832-
DOCK_SCORE_INTRA_KCAL0.471272-
DOCK_SCORE_INTRA_NORM0.112792-
DOCK_SCORE_INTRA_NORM0.125580-
DOCK_SCORE_INTRA_NORM0.068039-
DOCK_SCORE_KCAL-5.323806-
DOCK_SCORE_KCAL-5.243004-
DOCK_SCORE_KCAL-5.137028-
DOCK_SCORE_NORM-0.768609-
DOCK_SCORE_NORM-0.756945-
DOCK_SCORE_NORM-0.741643-
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_FILET09_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FILET17_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FORMULAC21H17Cl2N4O2+-
DOCK_SOURCE_FORMULAC21H17Cl2N4O2+-
DOCK_SOURCE_FORMULAC21H17Cl2N4O2+-
DOCK_SOURCE_HBA2.000000-
DOCK_SOURCE_HBA2.000000-
DOCK_SOURCE_HBA2.000000-
DOCK_SOURCE_HBD1.000000-
DOCK_SOURCE_HBD1.000000-
DOCK_SOURCE_HBD1.000000-
DOCK_SOURCE_HEAVY_ATOMS29.000000-
DOCK_SOURCE_HEAVY_ATOMS29.000000-
DOCK_SOURCE_HEAVY_ATOMS29.000000-
DOCK_SOURCE_LOGP3.200200-
DOCK_SOURCE_LOGP3.200200-
DOCK_SOURCE_LOGP3.200200-
DOCK_SOURCE_MW428.299000-
DOCK_SOURCE_MW428.299000-
DOCK_SOURCE_MW428.299000-
DOCK_SOURCE_NAMEulfkktlib_445-
DOCK_SOURCE_NAMEulfkktlib_2558-
DOCK_SOURCE_NAMEulfkktlib_445-
DOCK_SOURCE_RINGS4.000000-
DOCK_SOURCE_RINGS4.000000-
DOCK_SOURCE_RINGS4.000000-
DOCK_SOURCE_TPSA69.650000-
DOCK_SOURCE_TPSA69.650000-
DOCK_SOURCE_TPSA69.650000-
DOCK_STRAIN_DELTA62.628153-
DOCK_STRAIN_DELTA44.122041-
DOCK_STRAIN_DELTA38.166060-
DOCK_STRAIN_OK0-
DOCK_STRAIN_OK0-
DOCK_STRAIN_OK0-
DOCK_TARGETT09-
DOCK_TARGETT09-
DOCK_TARGETT17-
EXACT_MASS427.07230756409Da
FORMULAC21H17Cl2N4O2+-
HBA2-
HBD1-
LOGP3.2002000000000015-
MOL_WEIGHT428.29900000000015g/mol
QED_SCORE0.5306198872136143-
ROTATABLE_BONDS5-
TPSA69.65A^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 2
native pose available
 0.9729301669009104 -22.2897 15 0.71 - Best pose
T17 T17 selection_import_t17 1
native pose available
 1.1929798130975804 -21.5077 9 0.75 - Best pose
T09 — T09 2 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
171 0.9729301669009104 -0.881401 -22.2897 1 19 15 0.71 0.14 0.17 0.17 - no geometry warning; 12 clashes; 3 protein contact clashes; high strain Δ 62.6 Open pose
186 1.103341536226107 -0.882525 -21.9514 2 20 17 0.81 0.14 0.17 0.17 - no geometry warning; 10 clashes; 5 protein contact clashes; high strain Δ 44.1 Open pose
T17 — T17 1 poses · report selection_import_t17
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
208 1.1929798130975804 -0.809682 -21.5077 3 16 9 0.75 1.00 1.00 1.00 - no geometry warning; 11 clashes; 4 protein contact clashes; high strain Δ 38.2 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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