Rimegepant BMS-927711,99.83%

产品编号:Bellancom-15498| CAS NO:1289023-67-1| 分子式:C28H28F2N6O3| 分子量:534.56

本网站销售的所有产品仅用于工业应用或者科学研究等非医疗目的,不可用于人类或动物的临床诊断或者治疗,非药用,非食用,

货号 包装 价格 库存与货期 购买量 操作
Bellancom-15498
1200.00 杭州 北京(现货)
Bellancom-15498
1800.00 杭州 北京(现货)
Bellancom-15498
3700.00 杭州 北京(现货)
Bellancom-15498
5500.00 杭州 北京(现货)
Bellancom-15498
8500.00 杭州 北京(现货)

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Rimegepant BMS-927711

产品介绍 Rimegepant (BMS-927711) 是一种有效的降钙素基因相关肽 (CGRP) 受体拮抗剂,对 hCGRP 受体的 Ki 为 0.027 nM,IC50 为 0.14 nM。
生物活性

Rimegepant (BMS-927711) is a highly potent, oral calcitonin gene-related peptide (CGRP) receptor antagonist with a Ki of 0.027 nM and an IC50 of 0.14 nM for hCGRP receptor.

体外研究

Rimegepant (BMS-927711) is a full, competitive CGRP receptor antagonist with IC50 of 0.14±0.01 nM.

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

体内研究

Rimegepant (BMS-927711) has good oral bioavailability in rat and cynomolgus monkey, attractive overall preclinical properties, and shows dose-dependent activity in a primate model of CGRP-induced facial blood flow. The ratios of the mean AUC (0-24 h) values for Rimegepant (BMS-927711) (60, 100, and 300 mg/kg) in the DBS matrix, compare with plasma, are 0.5-0.6 across all doses in rats. Results from this study suggest a strong correlation of Rimegepant concentrations between rat plasma and rat blood (DBS).

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

体内研究

Rimegepant (BMS-927711) has good oral bioavailability in rat and cynomolgus monkey, attractive overall preclinical properties, and shows dose-dependent activity in a primate model of CGRP-induced facial blood flow. The ratios of the mean AUC (0-24 h) values for Rimegepant (BMS-927711) (60, 100, and 300 mg/kg) in the DBS matrix, compare with plasma, are 0.5-0.6 across all doses in rats. Results from this study suggest a strong correlation of Rimegepant concentrations between rat plasma and rat blood (DBS).

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

性状Solid
溶解性数据
In Vitro: 

DMSO : 10 mg/mL (18.71 mM; Need ultrasonic and warming)

Ethanol : 4.4 mg/mL (8.23 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 1.8707 mL 9.3535 mL 18.7070 mL
5 mM 0.3741 mL 1.8707 mL 3.7414 mL
10 mM 0.1871 mL 0.9353 mL 1.8707 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: 5% DMSO    40% PEG300    5% Tween-80    50% saline

    Solubility: ≥ 2.5 mg/mL (4.68 mM); Clear solution

  • 2.

    请依序添加每种溶剂: 10% EtOH    90% PEG300

    Solubility: ≥ 1 mg/mL (1.87 mM); Clear solution

*以上所有助溶剂都可在 西域 网站选购。
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
参考文献

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