Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetG-protein coupled estrogen receptor 1
LigandBDBM50459750
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1767035 (CHEMBL4202282)
EC50 480±n/a nM
Citation O'Dea, ASondergard, CSweeney, PArnatt, CK A Series of Indole-Thiazole Derivatives Act as GPER Agonists and Inhibit Breast Cancer Cell Growth. ACS Med Chem Lett9:901-906 (2018) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
G-protein coupled estrogen receptor 1
Name:G-protein coupled estrogen receptor 1
Synonyms:CEPR | CMKRL2 | DRY12 | G-protein coupled estrogen receptor 1 | G-protein-coupled receptor (GPR30 ) | GPER | GPER1 | GPER1_HUMAN | GPR30
Type:PROTEIN
Mol. Mass.:42259.21
Organism:Homo sapiens (Human)
Description:ChEMBL_982507
Residue:375
Sequence:
MDVTSQARGVGLEMYPGTAQPAAPNTTSPELNLSHPLLGTALANGTGELSEHQQYVIGLF
LSCLYTIFLFPIGFVGNILILVVNISFREKMTIPDLYFINLAVADLILVADSLIEVFNLH
ERYYDIAVLCTFMSLFLQVNMYSSVFFLTWMSFDRYIALARAMRCSLFRTKHHARLSCGL
IWMASVSATLVPFTAVHLQHTDEACFCFADVREVQWLEVTLGFIVPFAIIGLCYSLIVRV
LVRAHRHRGLRPRRQKALRMILAVVLVFFVCWLPENVFISVHLLQRTQPGAAPCKQSFRH
AHPLTGHIVNLAAFSNSCLNPLIYSFLGETFRDKLRLYIEQKTNLPALNRFCHAALKAVI
PDSTEQSDVRFSSAV
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50459750
n/a
NameBDBM50459750
Synonyms:CHEMBL4204670
TypeSmall organic molecule
Emp. Form.C15H13BrClN3OS
Mol. Mass.398.705
SMILESCCc1nc(NC(=O)c2[nH]c3ccc(Br)cc3c2Cl)sc1C
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: