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BDBM33843

E3L001810
Internal ID: BDB001810
Activity data available Local docking-ready structure
Dock with P00748
Structure
/e3_file/ligand_db/generated/BDB001810/BDB001810.sdf
Basic Properties
Compound ID
E3L001810
Internal ID
BDB001810
Molecular formula
C14H10FN5O
Molecular weight
283.266000
Exact mass
283.086938
XLogP
1.7499
TPSA
86.6900
HBA / HBD
5 / 1
Rotatable bonds
2
Heavy atoms / rings
21 / 3
Activity summary
IC50 unknown 81.00000000 nM
1 activity record(s) imported
InChIKey
FXRFMCDLHSKARY-UHFFFAOYSA-N
SMILES
Nc1nc(-c2cccnc2)nn1C(=O)c1ccc(F)cc1
Aliases
BDBM33843 (preferred) 1-(4-fluorobenzoyl)-3-(3-pyridinyl)-1H-1,2,4-triazol-5-amine (source_name) BDBM33843 (source_id)
E3 Relation
E3 UniProt Gene / protein Relation type Ligand role Direct Functional Docking Source Evidence
P00748 F12
Coagulation factor XII		 reported_binder bindingdb_reported Yes No low BindingDB:BDBM33843 medium
; target=Coagulation factor XII
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM33843 Open - 10.7270/Q21G0JQS
PubChem CID972160 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready Nc1nc(-c2cccnc2)nn1C(=O)c1ccc(F)cc1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB001810/BDB001810.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB001810/BDB001810.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB001810/BDB001810.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB001810/BDB001810.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB001810/BDB001810.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Coagulation factor XII
P00748
E3 ligase component 		BindingDB:BDBM33843 IC50 81 nM High DOI: 10.7270/Q21G0JQS 1