详细说明
Catalogue Number : 8819813
Description
G-1 is a selective potent agonist against the GPR30 receptor, an estradiol binding receptor that contributes to both uterine neurological responses. G-1 inhibits the production of lipopolysaccharide (LPS) induced cytokines such as IL-6 TNF-alpha. It is also reported to block MCF-1 cell cycle progression at the G1 phase display therapeutic effects in multiple sclerosis models.
Additional Information
Applications | FA |
Synonyms: | GPR30 Agonist, AC1MJFYZ, MLS001242405 |
Formulation: | Crystalline solid |
Chemical Name: | 1-[4-(6-bromo-1,3-benzodioxol-5-yl)-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinolin-8-yl]ethanone |
Molecular Formula: | C21H18BrNO3 |
Molecular Weight: | <div "class="productview-attribute-conten_div" style="margin: 0px; padding: 0px;">412.3 |
CAS Number
881639-98-1
Purity:
≥98%
Storage Conditions:
Product should be kept at -20°C.
References:
Bologa, C. G., Revankar, C. M., Young, S. M., Edwards, B. S., Arterburn, J. B., Kiselyov, A. S., ... & Prossnitz, E. R. (2006). Virtual biomolecular screening converge on a selective agonist for GPR30. Nature chemical biology,2(4), 207-212.
Blasko, E., Haskell, C. A., Leung, S., Gualtieri, G., Halks-Miller, M., Mahmoudi, M., ... & Horuk, R. (2009). Beneficial role of the GPR30 agonist G-1 in an animal model of multiple sclerosis. Journal of neuroimmunology, 214(1), 67-77.
Kumar, R., Balhuizen, A., Amisten, S., Lundquist, I., & Salehi, A. (2011). Insulinotropic antidiabetic effects of 17β-estradiol the GPR30 agonist G-1 on human pancreatic islets. Endocrinology, 152(7), 2568-2579.