FAIRMol

KB_chagas_51

ID 1030

DB Docking_panel_21This detail page is pinned to the current database context.
Back to results Open docking pose (6)
2D structure

SMILES: O=c1[nH]c(/C=C/c2cccc(OCCOc3ccccc3)c2)nc(O)c1[N+](=O)O

Formula: C20H18N3O6+ | MW: 396.3790000000001

LogP: 2.903300000000001 | TPSA: 124.75000000000003

HBA/HBD: 6/3 | RotB: 8

InChIKey: CIKSIOVPTBTPRY-MDZDMXLPSA-O

Recognized patterns

Click a named motif to highlight it in the 2D depiction or launch reverse search.
Highlighted: 1 pattern Ether Clear highlight

Bio motif

ATP mimic pyrimidine H-bond acceptor N ×2 H-bond acceptor O ×4 H-bond donor ×3 Gatekeeper aromatic ×2

Functional group

Phenol Aryl ether ×2 Ether ×2 Alkene

Ring system

Benzene ×2 Pyrimidine
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Properties

NameValueUnit
DOCK_BASE_INTER_RANK-0.735594-
DOCK_BASE_INTER_RANK-0.852866-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_BOND_LENGTH_OUTLIERS0.000000-
DOCK_CLASH_COUNT17.000000-
DOCK_CLASH_COUNT17.000000-
DOCK_CONTACT_COUNT10.000000-
DOCK_CONTACT_COUNT18.000000-
DOCK_EXPERIMENTT04-
DOCK_EXPERIMENTT07-
DOCK_EXPERIMENT_ID3-
DOCK_EXPERIMENT_ID5-
DOCK_FINAL_RANK8.891354-
DOCK_FINAL_RANK10.137609-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOMETRY_ALERTwarning-
DOCK_GEOM_OK0-
DOCK_GEOM_OK0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_HARD_GEOMETRY_FAIL0-
DOCK_IFP::A:ARG141-
DOCK_IFP::A:ARG171-
DOCK_IFP::A:ASP1611-
DOCK_IFP::A:CYS1681-
DOCK_IFP::A:GLN1661-
DOCK_IFP::A:GLY2251-
DOCK_IFP::A:HIS2411-
DOCK_IFP::A:LEU1881-
DOCK_IFP::A:LEU2081-
DOCK_IFP::A:LEU2091-
DOCK_IFP::A:LEU2261-
DOCK_IFP::A:LEU2291-
DOCK_IFP::A:MET1631-
DOCK_IFP::A:MET2131-
DOCK_IFP::A:NAP3011-
DOCK_IFP::A:NDP3021-
DOCK_IFP::A:PHE1131-
DOCK_IFP::A:PHE971-
DOCK_IFP::A:PRO1671-
DOCK_IFP::A:PRO2101-
DOCK_IFP::A:SER2071-
DOCK_IFP::A:SER951-
DOCK_IFP::A:TRP2211-
DOCK_IFP::A:TYR1741-
DOCK_IFP::A:TYR1941-
DOCK_IFP::A:VAL2061-
DOCK_IFP::D:ARG2871-
DOCK_IFP::D:HIS2671-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_IMPORT_SCOPEbest_by_name-
DOCK_MAX_CLASH_OVERLAP0.649633-
DOCK_MAX_CLASH_OVERLAP0.649667-
DOCK_POSE_COUNT4-
DOCK_POSE_COUNT2-
DOCK_PRE_RANK5.527571-
DOCK_PRE_RANK7.142768-
DOCK_PRIMARY_POSE_ID6823-
DOCK_PRIMARY_POSE_ID10877-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_RANKING_MODEinter_strain_penalized-
DOCK_REPORT_IDdockmulti_91311c650f2e_T04-
DOCK_REPORT_IDdockmulti_91311c650f2e_T07-
DOCK_RESIDUE_CONTACTSA:ARG17;A:GLY225;A:HIS241;A:LEU188;A:LEU226;A:LEU229;A:NDP302;A:PHE113;A:TYR194;D:ARG287-
DOCK_RESIDUE_CONTACTSA:ARG14;A:ASP161;A:CYS168;A:GLN166;A:LEU208;A:LEU209;A:MET163;A:MET213;A:NAP301;A:PHE97;A:PRO167;A:PRO210;A:SER207;A:SER95;A:TRP221;A:TYR174;A:VAL206;D:HIS267-
DOCK_SCAFFOLDO=c1ccnc(C=Cc2cccc(OCCOc3ccccc3)c2)[nH]1-
DOCK_SCAFFOLDO=c1ccnc(C=Cc2cccc(OCCOc3ccccc3)c2)[nH]1-
DOCK_SCORE-21.087000-
DOCK_SCORE-25.993800-
DOCK_SCORE_INTER-21.332200-
DOCK_SCORE_INTER-24.733100-
DOCK_SCORE_INTER_KCAL-5.095111-
DOCK_SCORE_INTER_KCAL-5.907402-
DOCK_SCORE_INTER_NORM-0.735594-
DOCK_SCORE_INTER_NORM-0.852866-
DOCK_SCORE_INTRA0.245249-
DOCK_SCORE_INTRA-1.260680-
DOCK_SCORE_INTRA_KCAL0.058577-
DOCK_SCORE_INTRA_KCAL-0.301108-
DOCK_SCORE_INTRA_NORM0.008457-
DOCK_SCORE_INTRA_NORM-0.043472-
DOCK_SCORE_KCAL-5.036546-
DOCK_SCORE_KCAL-6.208515-
DOCK_SCORE_NORM-0.727137-
DOCK_SCORE_NORM-0.896338-
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_T04_top1000.sdf-
DOCK_SOURCE_FILEresults_T07_top1000.sdf-
DOCK_SOURCE_FORMULAC20H18N3O6+-
DOCK_SOURCE_FORMULAC20H18N3O6+-
DOCK_SOURCE_HBA6.000000-
DOCK_SOURCE_HBA6.000000-
DOCK_SOURCE_HBD3.000000-
DOCK_SOURCE_HBD3.000000-
DOCK_SOURCE_HEAVY_ATOMS29.000000-
DOCK_SOURCE_HEAVY_ATOMS29.000000-
DOCK_SOURCE_LOGP2.903300-
DOCK_SOURCE_LOGP2.903300-
DOCK_SOURCE_MW396.379000-
DOCK_SOURCE_MW396.379000-
DOCK_SOURCE_NAMEKB_chagas_51-
DOCK_SOURCE_NAMEKB_chagas_51-
DOCK_SOURCE_RINGS3.000000-
DOCK_SOURCE_RINGS3.000000-
DOCK_SOURCE_TPSA124.750000-
DOCK_SOURCE_TPSA124.750000-
DOCK_STRAIN_DELTA68.063057-
DOCK_STRAIN_DELTA61.914013-
DOCK_STRAIN_OK0-
DOCK_STRAIN_OK0-
DOCK_TARGETT04-
DOCK_TARGETT07-
EXACT_MASS396.1190117160899Da
FORMULAC20H18N3O6+-
HBA6-
HBD3-
LOGP2.903300000000001-
MOL_WEIGHT396.3790000000001g/mol
QED_SCORE0.3948478118906239-
ROTATABLE_BONDS8-
TPSA124.75000000000003A^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
T04 T04 dockmulti_91311c650f2e_T04 4
native pose available
 8.891354461712035 -21.087 10 0.53 - Best pose
T07 T07 dockmulti_91311c650f2e_T07 2
native pose available
 10.137608898790562 -25.9938 14 0.74 - Best pose
T04 — T04 4 poses · report dockmulti_91311c650f2e_T04
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
236 8.891354461712035 -0.735594 -21.087 1 10 10 0.53 0.17 0.20 0.20 - no geometry warning; 17 clashes; 9 protein contact clashes; high strain Δ 68.1 Open pose
238 9.94565831720314 -0.764026 -16.0977 2 14 13 0.68 0.17 0.20 0.40 - yes excluded; geometry warning; 18 clashes; 1 protein clash; high strain Δ 80.9 Open pose
237 11.378385254109677 -0.859906 -25.2046 3 14 12 0.63 0.50 0.60 0.60 - yes excluded; geometry warning; 15 clashes; 3 protein clashes; high strain Δ 68.8 Open pose
239 14.360884061584606 -0.722768 -18.6849 3 13 12 0.63 0.33 0.40 0.40 - yes excluded; geometry warning; 15 clashes; 2 protein clashes; high strain Δ 91.1 Open pose
T07 — T07 2 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
439 10.137608898790562 -0.852866 -25.9938 7 18 14 0.74 0.33 0.40 0.40 - no geometry warning; 17 clashes; 15 protein contact clashes; high strain Δ 61.9 Open pose
440 11.16361976595469 -1.11752 -34.255 4 17 13 0.68 0.17 0.40 0.40 - no geometry warning; 17 clashes; 19 protein contact clashes; high strain Δ 64.3 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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