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Bromocriptine mesylate

CAS No. 22260-51-1

Bromocriptine mesylate ( CB-154 )

产品货号. M13556 CAS No. 22260-51-1

Bromocriptine (CB-154) is a dopamine D2 receptor agonist (Ki=3 nM) and and various serotonin receptors, also inhibits the release of glutamate by reversing the glutamate GLT1 transporter.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
100MG ¥478 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Bromocriptine mesylate
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    Bromocriptine (CB-154) is a dopamine D2 receptor agonist (Ki=3 nM) and and various serotonin receptors, also inhibits the release of glutamate by reversing the glutamate GLT1 transporter.
  • 产品描述
    Bromocriptine (CB-154) is a dopamine D2 receptor agonist (Ki=3 nM) and and various serotonin receptors, also inhibits the release of glutamate by reversing the glutamate GLT1 transporter; decreases body fat in animal and human models and increases lean muscle mass, improves glucose intolerance and insulin resistance, and reduces triglycerides and free fatty acids; also induces apoptosis and decreases colony formation in AML cells, shows synergy with standard agents and selectivity for the leukemic cell; reduces hyperphagia and adiposity in rats with diet-induced obesity.Diabetes Approved
  • 同义词
    CB-154
  • 通路
    GPCR/G Protein
  • 靶点
    Dopamine Receptor
  • 受体
    Dopamine Receptor
  • 研究领域
    Metabolic Disease
  • 适应症
    Diabetes

化学信息

  • CAS Number
    22260-51-1
  • 分子量
    750.70
  • 分子式
    C33H44BrN5O8S
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: ≥ 30 mg/mL
  • SMILES
    O=C([C@H](C=C12)CN(C)[C@]2([H])CC3=C(Br)NC4=C3C1=CC=C4)N[C@@](O5)(C(C)C)C(N6[C@]5(O)[C@@](CCC7)([H])N7C([C@@H]6CC(C)C)=O)=O.CS(=O)(O)=O
  • 化学全称
    Ergotaman-3',6',18-trione, 2-bromo-12'-hydroxy-2'-(1-methylethyl)-5'-(2-methylpropyl)-, (5α)-, methanesulfonate (1:1)

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1. Shirasaki Y, et al. Eur J Pharmacol. 2010 Sep 15;643(1):48-57.
2. Oda T, et al. Eur J Pharmacol. 2008 Nov 19;598(1-3):27-31.
3. Wacker J, et al. Psychophysiology. 2006 Jul;43(4):372-81.
4. Liberante FG, et al. Oncotarget. 2016 Feb 9;7(6):6609-19.
产品手册
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