FAIRMol

Z44848907

ID 278

DB Docking_panel_21This detail page is pinned to the current database context.
Back to results Open docking pose (12)
2D structure

SMILES: COc1cc(/C=N\NC(=O)c2ccc(CN3C(=O)c4cccc5cccc3c45)cc2)cc(OC)c1O

Formula: C28H23N3O5 | MW: 481.5080000000002

LogP: 4.486900000000004 | TPSA: 100.46000000000001

HBA/HBD: 6/2 | RotB: 7

InChIKey: DGIKUUDZEVZSNM-FDVSRXAVSA-N

Recognized patterns

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

Bio motif

Catechol ×2 Resorcinol Hinge binder (C=O-NH) Hinge binder (NH-C=O) N-Methyl amide ×2 H-bond acceptor N ×2 H-bond acceptor O ×4 H-bond donor ×2 Gatekeeper aromatic ×4 Metal chelator ×2 P-gp efflux flag

Functional group

Carbonyl ×2 Amide ×2 Phenol Tertiary amine Lactam Aryl ether ×2 Imine Ether ×2

Ring system

Benzene ×4 Naphthalene
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Properties

NameValueUnit
DOCK_BASE_INTER_RANK-0.707983-
DOCK_BASE_INTER_RANK-0.818501-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_CLASH_COUNT16.000000-
DOCK_CLASH_COUNT15.000000-
DOCK_CONTACT_COUNT19.000000-
DOCK_CONTACT_COUNT17.000000-
DOCK_EXPERIMENTT02-
DOCK_EXPERIMENTT07-
DOCK_EXPERIMENT_ID1-
DOCK_EXPERIMENT_ID5-
DOCK_FINAL_RANK5.335878-
DOCK_FINAL_RANK4.614541-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOM_OK0-
DOCK_GEOM_OK0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_IFP::A:ALA101-
DOCK_IFP::A:ALA2121-
DOCK_IFP::A:ARG141-
DOCK_IFP::A:ARG291-
DOCK_IFP::A:ASN651-
DOCK_IFP::A:ASP1611-
DOCK_IFP::A:CYS1681-
DOCK_IFP::A:GLU2171-
DOCK_IFP::A:GLU311-
DOCK_IFP::A:ILE611-
DOCK_IFP::A:ILE81-
DOCK_IFP::A:LEU2081-
DOCK_IFP::A:LEU2091-
DOCK_IFP::A:LEU231-
DOCK_IFP::A:LEU281-
DOCK_IFP::A:LEU681-
DOCK_IFP::A:LYS2201-
DOCK_IFP::A:MET2131-
DOCK_IFP::A:NAP2011-
DOCK_IFP::A:NAP3011-
DOCK_IFP::A:PHE1711-
DOCK_IFP::A:PHE321-
DOCK_IFP::A:PHE351-
DOCK_IFP::A:PHE971-
DOCK_IFP::A:PRO2101-
DOCK_IFP::A:PRO271-
DOCK_IFP::A:PRO621-
DOCK_IFP::A:PRO991-
DOCK_IFP::A:SER601-
DOCK_IFP::A:THR571-
DOCK_IFP::A:TRP2211-
DOCK_IFP::A:TYR1221-
DOCK_IFP::A:TYR1741-
DOCK_IFP::A:TYR981-
DOCK_IFP::A:VAL1161-
DOCK_IFP::A:VAL91-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_MAX_CLASH_OVERLAP0.680287-
DOCK_MAX_CLASH_OVERLAP0.664735-
DOCK_POSE_COUNT6-
DOCK_POSE_COUNT6-
DOCK_PRE_RANK4.205594-
DOCK_PRE_RANK3.750519-
DOCK_PRIMARY_POSE_ID3165-
DOCK_PRIMARY_POSE_ID12622-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_REPORT_IDdockmulti_91311c650f2e_T02-
DOCK_REPORT_IDdockmulti_91311c650f2e_T07-
DOCK_RESIDUE_CONTACTSA:ALA10;A:ARG29;A:ASN65;A:GLU31;A:ILE61;A:ILE8;A:LEU23;A:LEU28;A:LEU68;A:NAP201;A:PHE32;A:PHE35;A:PRO27;A:PRO62;A:SER60;A:THR57;A:TYR122;A:VAL116;A:VAL9-
DOCK_RESIDUE_CONTACTSA:ALA212;A:ARG14;A:ASP161;A:CYS168;A:GLU217;A:LEU208;A:LEU209;A:LYS220;A:MET213;A:NAP301;A:PHE171;A:PHE97;A:PRO210;A:PRO99;A:TRP221;A:TYR174;A:TYR98-
DOCK_SCAFFOLDO=C(NN=Cc1ccccc1)c1ccc(CN2C(=O)c3cccc4cccc2c34)cc1-
DOCK_SCAFFOLDO=C(NN=Cc1ccccc1)c1ccc(CN2C(=O)c3cccc4cccc2c34)cc1-
DOCK_SCORE-27.762800-
DOCK_SCORE-26.249100-
DOCK_SCORE_INTER-25.487400-
DOCK_SCORE_INTER-29.466000-
DOCK_SCORE_INTER_KCAL-6.087564-
DOCK_SCORE_INTER_KCAL-7.037836-
DOCK_SCORE_INTER_NORM-0.707983-
DOCK_SCORE_INTER_NORM-0.818501-
DOCK_SCORE_INTRA-2.275430-
DOCK_SCORE_INTRA3.216950-
DOCK_SCORE_INTRA_KCAL-0.543477-
DOCK_SCORE_INTRA_KCAL0.768356-
DOCK_SCORE_INTRA_NORM-0.063206-
DOCK_SCORE_INTRA_NORM0.089360-
DOCK_SCORE_KCAL-6.631034-
DOCK_SCORE_KCAL-6.269493-
DOCK_SCORE_NORM-0.771190-
DOCK_SCORE_NORM-0.729141-
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_T02_top1000.sdf-
DOCK_SOURCE_FILEresults_T07_top1000.sdf-
DOCK_SOURCE_FORMULAC28H23N3O5-
DOCK_SOURCE_FORMULAC28H23N3O5-
DOCK_SOURCE_HBA6.000000-
DOCK_SOURCE_HBA6.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HBD2.000000-
DOCK_SOURCE_HEAVY_ATOMS36.000000-
DOCK_SOURCE_HEAVY_ATOMS36.000000-
DOCK_SOURCE_LOGP4.486900-
DOCK_SOURCE_LOGP4.486900-
DOCK_SOURCE_MW481.508000-
DOCK_SOURCE_MW481.508000-
DOCK_SOURCE_NAMEZ44848907-
DOCK_SOURCE_NAMEZ44848907-
DOCK_SOURCE_RINGS5.000000-
DOCK_SOURCE_RINGS5.000000-
DOCK_SOURCE_TPSA100.460000-
DOCK_SOURCE_TPSA100.460000-
DOCK_STRAIN_DELTA30.838061-
DOCK_STRAIN_DELTA26.400359-
DOCK_STRAIN_OK0-
DOCK_STRAIN_OK0-
DOCK_TARGETT02-
DOCK_TARGETT07-
EXACT_MASS481.163770836Da
FORMULAC28H23N3O5-
HBA6-
HBD2-
LOGP4.486900000000004-
MOL_WEIGHT481.5080000000002g/mol
QED_SCORE0.29934799557302927-
ROTATABLE_BONDS7-
TPSA100.46000000000001A^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
T07 T07 dockmulti_91311c650f2e_T07 6
native pose available
 4.614540518243182 -26.2491 14 0.74 - Best pose
T02 T02 dockmulti_91311c650f2e_T02 6
native pose available
 5.335877589857202 -27.7628 16 0.76 - Best pose
T07 — T07 6 poses · report dockmulti_91311c650f2e_T07
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
2184 4.614540518243182 -0.818501 -26.2491 2 17 14 0.74 0.00 0.00 0.00 - no geometry warning; 15 clashes; 4 protein contact clashes; high strain Δ 26.4 Open pose
2183 4.68727944917791 -0.690042 -22.7785 0 15 13 0.68 0.00 0.00 0.00 - no geometry warning; 18 clashes; 4 protein contact clashes; moderate strain Δ 18.5 Open pose
2186 5.879476557389142 -0.795684 -32.7539 1 13 13 0.68 0.00 0.00 0.00 - no geometry warning; 16 clashes; 7 protein contact clashes; high strain Δ 32.3 Open pose
2187 6.585916680181024 -0.695498 -23.5563 0 14 13 0.68 0.00 0.00 0.00 - yes excluded; geometry warning; 18 clashes; 1 protein clash; high strain Δ 23.8 Open pose
2188 6.638558359145298 -0.782849 -29.2739 0 15 12 0.63 0.00 0.00 0.00 - yes excluded; geometry warning; 15 clashes; 1 protein clash; high strain Δ 25.4 Open pose
2185 8.632533309205227 -0.784229 -32.4514 5 16 12 0.63 0.17 0.20 0.40 - yes excluded; geometry warning; 15 clashes; 1 protein clash; high strain Δ 33.4 Open pose
T02 — T02 6 poses · report dockmulti_91311c650f2e_T02
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
3165 5.335877589857202 -0.707983 -27.7628 1 19 16 0.76 0.20 0.20 0.20 - no geometry warning; 16 clashes; 5 protein contact clashes; high strain Δ 30.8 Open pose
3160 7.490407099445143 -0.580747 -17.3863 3 17 15 0.71 0.20 0.20 0.40 - no geometry warning; 17 clashes; 10 protein contact clashes; high strain Δ 38.4 Open pose
3161 7.882129821552622 -0.72906 -17.4267 3 16 13 0.62 0.00 0.20 0.20 - no geometry warning; 21 clashes; 9 protein contact clashes; high strain Δ 41.7 Open pose
3163 9.230738807532372 -0.704018 -30.3141 3 19 18 0.86 0.20 0.20 0.20 - yes excluded; geometry warning; 18 clashes; 2 protein clashes; high strain Δ 35.8 Open pose
3164 12.54575112579421 -0.692076 -22.3496 3 21 17 0.81 0.20 0.20 0.20 - yes excluded; geometry warning; 14 clashes; 3 protein clashes; high strain Δ 30.2 Open pose
3162 13.238925520518073 -0.678001 -25.0814 6 20 16 0.76 0.20 0.20 0.20 - yes excluded; geometry warning; 16 clashes; 3 protein clashes; high strain Δ 36.4 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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