1. GPCR/G Protein
  2. GHSR
  3. BMS-604992

BMS-604992  (Synonyms: EX-1314)

目录号: HY-14495
产品使用指南

BMS-604992 (EX-1314) 是一种选择性的口服活性小分子 growth hormone secretagogue receptor (GHSR) 激动剂。BMS-604992 具有高亲和力 (ki=2.3 nM) 和强大的功能活性 (EC50=0.4 nM)。BMS-604992 能刺激啮齿动物进食。

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BMS-604992 Chemical Structure

BMS-604992 Chemical Structure

CAS No. : 674343-47-6

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查看 GHSR 亚型特异性产品:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

BMS-604992 (EX-1314) is a selective, orally active small-molecule growth hormone secretagogue receptor (GHSR) agonist. BMS-604992 demonstrates high-affinity binding (Ki=2.3 nM) and potent functional activity (EC50=0.4 nM). BMS-604992 can stimulate food intake in rodents[1].

IC50 & Target

EC50: 0.4 nM (GHSR), Ki: 2.3 nM (GHSR)[1]

体外研究
(In Vitro)

BMS-604992 exhibits high-affinity binding (Ki=2.3 nM) and potent functional activity (EC50=0.4 nM) for ghrelin receptor[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

BMS-604992 (500 μg/kg; i.p.; 5 minutes) results in a significant increase in gastric emptying compared with vehicle-treated mice[1].
BMS-604992 (1~1000 mg/kg; p.o.; 1 hour) Shows a dose-linear increase in plasma concentrations at the 1 hour time point and elicits a dose-responsive increase in food intake relative to vehicle-treated controls, with a minimum effective dose of approximately 10 mg/kg[1].
BMS-604992 (300 mg/kg; p.o.; 5~20 minutes) produces a significant difference at the 5 minutes time point.[1].
BMS-604992 (500 μg/kg; i.p.; 4 hours) increases food intake approximately 2-fold compared with vehicle-treated controls[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: C57BL/6 mice
Dosage: 500 μg/kg
Administration: I.p.; 5 minutes
Result: Resulted in a significant increase in gastric emptying compared with vehicle-treated mice.
Animal Model: C57BL/6 mice
Dosage: 1~1000 mg/kg
Administration: P.o.; 1 hour
Result: Showed a dose-linear increase in plasma concentrations at the 1 hour time point and elicited a dose-responsive increase in food intake relative to vehicle-treated controls, with a minimum effective dose of approximately 10 mg/kg.
Animal Model: SD rat
Dosage: 300 mg/kg
Administration: P.o.; 5~20 minutes
Result: Observed a significant difference at the 5 minutes time point.
Animal Model: Male GhrR KO and WT mice
Dosage: 500 μg/kg
Administration: I.p.; 4 hours
Result: Increased food intake approximately 2-fold compared with vehicle-treated controls.
分子量

534.01

Formula

C24H32ClN7O5

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献

BMS-604992 相关分类

  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
BMS-604992
目录号:
HY-14495
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