< Back to small molecule database

BDBM50434414

E3L055971
Internal ID: BDB055971
Activity data available Local docking-ready structure
Dock with P00797
Structure
/e3_file/ligand_db/generated/BDB055971/BDB055971.sdf
Basic Properties
Compound ID
E3L055971
Internal ID
BDB055971
Molecular formula
C26H43ClN4O3
Molecular weight
495.108000
Exact mass
494.302369
XLogP
3.2800
TPSA
98.9000
HBA / HBD
5 / 3
Rotatable bonds
9
Heavy atoms / rings
34 / 2
Activity summary
IC50 unknown 1.00000000 nM
1 activity record(s) imported
InChIKey
NEQDILQJMJOEBZ-VCOUNFBDSA-N
SMILES
CC(C)[C@H](C[C@H](O)[C@@H](N)CN1CC(=O)N(c2ccccc2Cl)CC1(C)C)C(=O)NCC(C)(C)C
Aliases
BDBM50434414 (preferred) (2S,4S,5S)-5-amino-6-[4-(2-chlorophenyl)-2,2-dimethyl-5-oxopiperazin-1-yl]-N-(2,2-dimethylpropyl)-4-hydroxy-2-propan-2-ylhexanamide (source_name) BDBM50434414 (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:BDBM50434414 medium
; target=Renin
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50434414 Open - 10.1016/j.bmc.2013.03.022 PMID: 23598247
PubChem CID66645882 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)NCC(C)(C)C keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB055971/BDB055971.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB055971/BDB055971.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB055971/BDB055971.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB055971/BDB055971.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB055971/BDB055971.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Renin
P00797
E3 ligase component 		BindingDB:BDBM50434414 IC50 1 nM Very high DOI: 10.1016/j.bmc.2013.03.022
PMID: 23598247 		1