BGC-20-1531 free base

(Synonyms: PGN 1531 free base)
目录号: PL09088 纯度: ≥98%
BGC-20-1531 (PGN 1531) free base 是一种有效的选择性前列腺素 EP4 受体拮抗剂, pKB 值为 7.6。BGC-20-1531 free base 具有研究偏头痛的潜力。
CAS No. :736183-35-0
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中文名称
BGC-20-1531 free base
英文名称
BGC-20-1531 free base
英文别名
9QV7JG4XYZ;4-[[4-(5-methoxypyridin-2-yl)phenoxy]methyl]-5-methyl-N-(2-methylphenyl)sulfonylfuran-2-carboxamide;BDBM50012545;SB18900;4-((4-(5-Methoxypyridin-2-yl)phenoxy)methyl)-5-methyl-N-(o-tolylsulfonyl)furan-2-carboxamide;4-[[4-(5-Methoxy-2-pyridinyl)phenoxy]methyl]-5-methyl-N-[(2-methylphenyl)sulfonyl]-2-furancarboxamide;BGC-20-1531 free base
Cas No.
736183-35-0
分子式
C26H24N2O6S
分子量
492.54
包装储存
Powder -20°C 3 years;4°C 2 years
详情描述
BGC-20-1531 (PGN 1531) free base 是一种有效的选择性前列腺素 EP4 受体拮抗剂, pKB 值为 7.6。BGC-20-1531 free base 具有研究偏头痛的潜力。
产品详情
BGC-20-1531 (PGN 1531) free base 是一种有效的选择性前列腺素 EP4 受体拮抗剂, pKB 值为 7.6。BGC-20-1531 free base 具有研究偏头痛的潜力。
生物活性
BGC-20-1531 (PGN 1531) free base is a potent and selective prostanoid EP 4 receptor antagonist, with a pK B of 7.6. BGC-20-1531 free base has the potential for the research of migraine headache.
性状
Solid
IC50 & Target[1][2]
pKB: 7.6 (prostanoid EP4 receptor)
体外研究(In Vitro)
BGC-20-1531 free base competitively antagonized PGE2-induced vasodilatation of human middle cerebral (pKb=7.8) and meningeal (pKb=7.6) arteries, but had no effect on responses induced by PGE2 on coronary, pulmonary or renal arteries. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
BGC-20-1531 free base (1-10 mg/kg; i.v.) causes a dose-dependent antagonism of the PGE 2 -induced increase in canine carotid blood flow. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
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
参考文献
[1]. Maubach KA, et al. BGC20-1531, a novel, potent and selective prostanoid EP receptor antagonist: a putative new treatment for migraine headache. Br J Pharmacol. 2009;156(2):316-327.
溶解度数据
In Vitro: DMSO : 250 mg/mL (507.57 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)
[1]. Maubach KA, et al. BGC20-1531, a novel, potent and selective prostanoid EP receptor antagonist: a putative new treatment for migraine headache. Br J Pharmacol. 2009;156(2):316-327.

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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