Pelecopan

目录号: GC69684纯度: >97.00%同义词: BCX9930
Pelecopan (BCX9930) 是一种有效的、选择性的补体因子 D 抑制剂,具有口服活性。IC50 值为 14.3 nM。Pelecopan 可靶向补体因子 D 以预防 PNH 中的血管内和血管外溶血,也可用于其他替代途径介导的疾病。

Pelecopan
Cas No.: 2378380-49-3
规格价格库存数量操作
10mg¥6,300.00现货
1
25mg¥13,320.00现货
1

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产品描述 Description

IC50: 14.3 nM (complement factor D)[1]

Pelecopan (BCX9930) is a potent, selective, orally active inhibitor of complement factor D to prevent both intravascular and extravascular hemolysis in PNH. Pelecopan also be used for other alternative pathway (AP) mediated diseases[1][2][3].

Pelecopan has a potent, highly specific inhibitory activity for purified human factor D with an IC50 value of 14.3 nM and also inhibits its proteolytic activity against factor B bound to C3b with an IC50 of 28.1 nM[1].
Pelecopan completely blocks hemolysis of PNH cells in vitro (with an IC50 value of 29.5 nM in rabbit erythrocytes) and suppresses the accumulation of C3 fragments on PNH erythrocytes[1].

[1]. International Nonproprietary Names for Pharmaceutical Substances (INN)
[2]. AustinKulasekararajMD MRCP, FRCPath, et al. BCX9930, a Potent, Selective, Oral Factor D Inhibitor, Demonstrates Proof-of-Concept As Monotherapy in Patients with Paroxysmal Nocturnal Hemoglobinuria (PNH). Blood (2020) Volume 136, Supplement 1, 5 November 2
[3]. XilinChenMDPhD, et al. Preclinical Characterization of BCX9930, a Potent Oral Complement Factor D Inhibitor, Targeting Alternative Pathway-Mediated Diseases Including Paroxysmal Nocturnal Hemoglobinuria (PNH). Blood (2020) Volume 136, Supplement 1, 5 Nove

产品文档 Product Documents

Purity:>97.00%

化学性质Chemical Properties

CAS 号
2378380-49-3
同义词
BCX9930
分子式
C23H19FN2O4
分子量
406.41 g/mol
溶解性
DMSO : 100 mg/mL (246.06 mM; Need ultrasonic)
保存条件
Store at -20°C
General tips
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 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol