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G-1 10mg

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產(chǎn)品介紹

    基本參數(shù)

    詳細(xì)說(shuō)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.

    product image

    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 neuroimmunology214(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. Endocrinology152(7), 2568-2579.

     

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