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BDBM50350916

E3L053584
Internal ID: BDB053584
Activity data available Local docking-ready structure
Dock with P00797
Structure
/e3_file/ligand_db/generated/BDB053584/BDB053584.sdf
Basic Properties
Compound ID
E3L053584
Internal ID
BDB053584
Molecular formula
C30H41ClN2O5
Molecular weight
545.120000
Exact mass
544.270400
XLogP
3.8993
TPSA
105.2500
HBA / HBD
6 / 3
Rotatable bonds
10
Heavy atoms / rings
38 / 4
Activity summary
IC50 unknown 1.10000000 nM
1 activity record(s) imported
InChIKey
VPBFTBGCWRVDOS-QHXQRBBOSA-N
SMILES
CCc1cccc(-c2c(Cl)cccc2[C@](O)(CCCCOC)[C@H]2CN(C(=O)[C@H]3C[C@@H](N)[C@@H](O)C3)CCO2)c1
Aliases
BDBM50350916 (preferred) [(1S,3R,4S)-3-amino-4-hydroxycyclopentyl]-[(2R)-2-[(1R)-1-[3-chloro-2-(3-ethylphenyl)phenyl]-1-hydroxy-5-methoxypentyl]morpholin-4-yl]methanone (source_name) BDBM50350916 (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:BDBM50350916 medium
; target=Renin
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50350916 Open - 10.1016/j.bmcl.2011.06.043 PMID: 21741239
PubChem CID53379391 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CCc1cccc(-c2c(Cl)cccc2[C@](O)(CCCCOC)[C@H]2CN(C(=O)[C@H]3C[C@@H](N)[C@@H](O)C3)CCO2)c1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB053584/BDB053584.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB053584/BDB053584.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB053584/BDB053584.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB053584/BDB053584.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB053584/BDB053584.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Renin
P00797
E3 ligase component 		BindingDB:BDBM50350916 IC50 1.1 nM Very high DOI: 10.1016/j.bmcl.2011.06.043
PMID: 21741239 		1