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  • SR1078

    • SR 1078, SR-1078
    货号: abs811752
    CAS号: 1246525-60-9
    分子式: C17H10F9NO2
    分子量: 431.25
    产品说明书
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    货号-规格 货期 价格 数量
    abs811752-5mg 1-2周 ¥992.00
    - +
    abs811752-10mg 1-2周 ¥1548.00
    - +
    abs811752-50mg 1-2周 ¥7095.00
    - +
    大包装询价
    产品描述
    描述

    SR1078 is an agonist of retinoic acid receptor-related orphan receptors (ROR) ROR??/??; increases transcription of ROR?? target genes; thought to increase p53 stability.

    纯度
    >98%
    储存/保存方法
    Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
    基本信息
    别名
    SR 1078, SR-1078
    可溶性/溶解性
    10 mM in DMSO
    生物活性
    靶点
    ROR
    In vitro(体外研究)
    SR1078 is a synthetic RORα/RORγ ligand. SR1078 modulates the conformation of RORγ in a biochemical assay and activates RORα and RORγ driven transcription. Furthermore, SR1078 stimulates expression of endogenous ROR target genes in HepG2 cells that express both RORα and RORγ. In a cell-based chimeric receptor Gal4 DNA-binding domain-NR ligand binding domain cotransfection assay, SR1078 significantly inhibits the constitutive transactivation activity of RORα and RORγ, but has no effect on the activity of FXR, LXRα and LXRβ. In a RORα cotransfection assay, treatment of cells with SR1078 (10 μM) results in a significant increase in transcription. Similarly, in the RORγ cotransfection assay, SR1078 treatment results in a stimulation of RORγ-dependent transcription activity.
    In vivo(体内研究)
    The pharmacokinetic properties of SR1078 are examined in mice and noted significant exposure. Plasma concentrations reach 3.6 μM 1h after a 10 mg/kg i.p. injection of SR1078 and sustained levels of above 800 nM even 8h after the single injection. These levels are sufficient to perform a proof-of-principle experiment to determine if SR1078 treatment would stimulate ROR target gene expression in an animal model. Mice are treated with SR1078 (10 mg/kg i.p.) and 2h after the injection the livers are harvested and mRNA purified for assessment of G6Pase and FGF21 gene expression.T he expression of both FGF21 and G6Pase is significantly stimulated by SR1078 treatment vs. vehicle control.
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    • 实验方法 实验条件
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