FAIRMol

TC265

ID 3319

DB fairmolThis detail page is pinned to the current database context.
Back to results Open docking pose (1)
2D structure

SMILES: C[C@]12CC[C@H](O)CC1=C/C(=N/OCC(=O)NCCOCCOCCNC(=O)CCCC[C@@H]1SC[C@@H]3NC(=O)N[C@@H]31)[C@H]1[C@H]2CC[C@@]2(C)[C@H]1CC[C@@]21O[C@@H]1CO

Formula: C39H61N5O9S | MW: 776.01

LogP: 2.413900000000006 | TPSA: 192.36999999999998

HBA/HBD: 11/6 | RotB: 18

InChIKey: DZUDXXOURUNHQM-WKLWBTFBSA-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) ×4 Hinge binder (NH-C=O) ×4 H-bond acceptor N H-bond acceptor O ×7 H-bond donor ×6 β-Turn mimetic Metal chelator ×4 Lipinski HMW fragment

Functional group

Carbonyl ×3 Amide ×4 Secondary amine ×4 Alcohol ×2 Lactam ×2 Epoxide Urea Sulfide Imine Ether ×3 Alkene

Ring system

Cyclohexane ×2 Imidazolidine Oxirane Cyclopentane Thiolane

Properties

NameValueUnit
DOCK_BASE_INTER_RANK-0.479431-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_CLASH_COUNT9.000000-
DOCK_CONTACT_COUNT22.000000-
DOCK_EXPERIMENTT09-
DOCK_EXPERIMENT_ID9-
DOCK_FINAL_RANK3.000118-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOM_OK0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_IFP::A:NDP3011-
DOCK_IFP::B:ALA321-
DOCK_IFP::B:ARG481-
DOCK_IFP::B:ARG971-
DOCK_IFP::B:ASP521-
DOCK_IFP::B:GLY1571-
DOCK_IFP::B:ILE451-
DOCK_IFP::B:LEU941-
DOCK_IFP::B:LYS571-
DOCK_IFP::B:LYS951-
DOCK_IFP::B:MET531-
DOCK_IFP::B:PHE561-
DOCK_IFP::B:PHE911-
DOCK_IFP::B:PRO501-
DOCK_IFP::B:PRO931-
DOCK_IFP::B:THR541-
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_MAX_CLASH_OVERLAP0.553889-
DOCK_POSE_COUNT1-
DOCK_PRE_RANK2.817265-
DOCK_PRIMARY_POSE_ID5609-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_REPORT_IDselection_import_t09-
DOCK_RESIDUE_CONTACTSA:NDP301;B:ALA32;B:ARG48;B:ARG97;B:ASP52;B:GLY157;B:ILE45;B:LEU94;B:LYS57;B:LYS95;B:MET53;B:PHE56;B:PHE91;B:PRO50;B:PRO93;B:THR54;B:TRP47;B:TYR162;B:VAL156;B:VAL30;B:VAL31;B:VAL49-
DOCK_SCAFFOLDO=C(CCCCC1SCC2NC(=O)NC21)NCCOCCOCCNC(=O)CON=C1C=C2CCCCC2C2CCC3C(CCC34CO4)C12-
DOCK_SCORE-15.781000-
DOCK_SCORE_INTER-25.889300-
DOCK_SCORE_INTER_KCAL-6.183556-
DOCK_SCORE_INTER_NORM-0.479431-
DOCK_SCORE_INTRA10.108200-
DOCK_SCORE_INTRA_KCAL2.414303-
DOCK_SCORE_INTRA_NORM0.187190-
DOCK_SCORE_KCAL-3.769229-
DOCK_SCORE_NORM-0.292241-
DOCK_SCORE_RESTR0.000000-
DOCK_SCORE_RESTR_NORM0.000000-
DOCK_SCORE_SYSTEM0.000000-
DOCK_SCORE_SYSTEM_NORM0.000000-
DOCK_SELECTION_EXCLUDED0-
DOCK_SEVERE_CLASH_COUNT0.000000-
DOCK_SOURCE_FILET09_top5_kcal_zscore_compound_names.sdf-
DOCK_SOURCE_FORMULAC39H61N5O9S-
DOCK_SOURCE_HBA11.000000-
DOCK_SOURCE_HBD6.000000-
DOCK_SOURCE_HEAVY_ATOMS54.000000-
DOCK_SOURCE_LOGP2.413900-
DOCK_SOURCE_MW776.010000-
DOCK_SOURCE_NAMETC265-
DOCK_SOURCE_RINGS7.000000-
DOCK_SOURCE_TPSA192.370000-
DOCK_STRAIN_DELTA85.852853-
DOCK_STRAIN_OK0-
DOCK_TARGETT09-
EXACT_MASS775.4189995319999Da
FORMULAC39H61N5O9S-
HBA11-
HBD6-
LOGP2.413900000000006-
MOL_WEIGHT776.01g/mol
QED_SCORE0.05219174121377488-
ROTATABLE_BONDS18-
TPSA192.36999999999998A^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
 3.0001177876563068 -15.781 15 0.71 - 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
191 3.0001177876563068 -0.479431 -15.781 9 22 15 0.71 0.29 0.33 0.50 - no geometry warning; 9 clashes; 1 protein clash; high strain Δ 85.9 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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