< Back to small molecule database

BDBM50434436

E3L055993
Internal ID: BDB055993
Activity data available Local docking-ready structure
Dock with P00797
Structure
/e3_file/ligand_db/generated/BDB055993/BDB055993.sdf
Basic Properties
Compound ID
E3L055993
Internal ID
BDB055993
Molecular formula
C27H35ClF2N4O3
Molecular weight
537.051000
Exact mass
536.236575
XLogP
4.0346
TPSA
98.9000
HBA / HBD
5 / 3
Rotatable bonds
9
Heavy atoms / rings
37 / 3
Activity summary
IC50 unknown 2.00000000 nM
1 activity record(s) imported
InChIKey
JBHCRIUYMONBCX-XZOYJPPVSA-N
SMILES
CC(C)[C@H](C[C@H](O)[C@@H](N)CN1CC(=O)N(c2ccccc2Cl)CC1(C)C)C(=O)Nc1ccc(F)cc1F
Aliases
BDBM50434436 (preferred) (2S,4S,5S)-5-amino-6-[4-(2-chlorophenyl)-2,2-dimethyl-5-oxopiperazin-1-yl]-N-(2,4-difluorophenyl)-4-hydroxy-2-propan-2-ylhexanamide (source_name) BDBM50434436 (source_id)
E3 Relation
E3 UniProt Gene / protein Relation type Ligand role Direct Functional Docking Source Evidence
P00797 REN
Renin		 reported_binder bindingdb_reported Yes No low BindingDB:BDBM50434436 medium
; target=Renin
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50434436 Open - 10.1016/j.bmc.2013.03.022 PMID: 23598247
PubChem CID71660109 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CC(C)[C@H](C[C@H](O)[C@@H](N)CN1CC(=O)N(c2ccccc2Cl)CC1(C)C)C(=O)Nc1ccc(F)cc1F keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB055993/BDB055993.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB055993/BDB055993.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB055993/BDB055993.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB055993/BDB055993.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB055993/BDB055993.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Renin
P00797
E3 ligase component 		BindingDB:BDBM50434436 IC50 2 nM Very high DOI: 10.1016/j.bmc.2013.03.022
PMID: 23598247 		1