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BDBM50215723

E3L048724
Internal ID: BDB048724
Activity data available Local docking-ready structure
Dock with P37231
Structure
/e3_file/ligand_db/generated/BDB048724/BDB048724.sdf
Basic Properties
Compound ID
E3L048724
Internal ID
BDB048724
Molecular formula
C26H23N3O5
Molecular weight
457.486000
Exact mass
457.163771
XLogP
4.7049
TPSA
113.0100
HBA / HBD
4 / 3
Rotatable bonds
7
Heavy atoms / rings
34 / 5
Activity summary
IC50 unknown 1000.00000000 nM
1 activity record(s) imported
InChIKey
BZVMWIDZSUXMLN-UHFFFAOYSA-N
SMILES
CC1=NC(=O)NC(c2ccc(OCCOc3cccc4[nH]c5ccccc5c34)cc2)C1C(=O)O
Aliases
BDBM50215723 (preferred) 4-(4-(2-(9H-carbazol-4-yloxy)ethoxy)phenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid (source_name) BDBM50215723 (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:BDBM50215723 medium
; target=Peroxisome proliferator-activated receptor gamma
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50215723 Open - 10.1016/j.bmcl.2007.05.081 PMID: 17574414
PubChem CID91935988 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CC1=NC(=O)NC(c2ccc(OCCOc3cccc4[nH]c5ccccc5c34)cc2)C1C(=O)O keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB048724/BDB048724.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB048724/BDB048724.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB048724/BDB048724.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB048724/BDB048724.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB048724/BDB048724.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component 		BindingDB:BDBM50215723 IC50 1000 nM Moderate DOI: 10.1016/j.bmcl.2007.05.081
PMID: 17574414 		1