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BDBM50344330

E3L053283
Internal ID: BDB053283
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB053283/BDB053283.sdf
Basic Properties
Compound ID
E3L053283
Internal ID
BDB053283
Molecular formula
C26H26FNO5
Molecular weight
451.494000
Exact mass
451.179501
XLogP
5.2099
TPSA
84.8600
HBA / HBD
4 / 2
Rotatable bonds
10
Heavy atoms / rings
33 / 3
Activity summary
EC50 unknown 5.00000000 nM
2 activity record(s) imported
InChIKey
AWMUDSVYMAZNQC-SFHVURJKSA-N
SMILES
CC[C@@H](Cc1ccc(OC)c(CNC(=O)c2ccc(Oc3ccc(F)cc3)cc2)c1)C(=O)O
Aliases
BDBM50344330 (preferred) (S)-2-(3-((4-(4-Fluorophenoxy)benzamido)methyl)-4-methoxybenzyl)butanoic acid (source_name) BDBM50344330 (source_id)
E3 Relation
E3 UniProt Gene / protein Relation type Ligand role Direct Functional Docking Source Evidence
P37231 PPARG;NR1C3
Peroxisome proliferator-activated receptor gamma
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50344330 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50344330 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50344330 Open - 10.1016/j.bmc.2011.03.064 PMID: 21530275
PubChem CID54581535 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CC[C@@H](Cc1ccc(OC)c(CNC(=O)c2ccc(Oc3ccc(F)cc3)cc2)c1)C(=O)O keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB053283/BDB053283.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB053283/BDB053283.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB053283/BDB053283.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB053283/BDB053283.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB053283/BDB053283.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50344330 EC50 5 nM Very high DOI: 10.1016/j.bmc.2011.03.064
PMID: 21530275
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50344330 EC50 920 nM Moderate DOI: 10.1016/j.bmc.2011.03.064
PMID: 21530275
1