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Ac-Arg-Cys-Met-5-aminopentanoyl-Arg-Val-Tyr-5-aminopentanoyl-Cys-NH2 trifluoroacetate salt (Disulfide bond)

更新时间:2024-07-22 15:01:30

Ac-Arg-Cys-Met-5-aminopentanoyl-Arg-Val-Tyr-5-aminopentanoyl-Cys-NH2 trifluoroacetate salt (Disulfide bond)结构式
Ac-Arg-Cys-Met-5-aminopentanoyl-Arg-Val-Tyr-5-aminopentanoyl-Cys-NH2 trifluoroacetate salt (Disulfide bond)结构式
品牌特惠专场
常用名 Ac-Arg-Cys-Met-5-aminopentanoyl-Arg-Val-Tyr-5-aminopentanoyl-Cys-NH2 trifluoroacetate salt (Disulfide bond) 英文名 Ac-Arg-Cys-Met-5-aminopentanoyl-Arg-Val-Tyr-5-aminopentanoyl-Cys-NH2 trifluoroacetate salt (Disulfide bond)
CAS号 353487-64-6 分子量 1167.471
密度 1.4±0.1 g/cm3 沸点 N/A
分子式 C49H82N16O11S3 熔点 N/A
MSDS N/A 闪点 N/A

 用途


hMCH-1R拮抗剂1(化合物30)是具有3.6nM的KB值的人黑色素浓缩激素受体1(hMCHR1)的有效且选择性的拮抗剂。HMCH-1R拮抗剂1可以分别以65nM和49nM的IC50值与hMCHR1和hMCHR2结合。HMCH-1R拮抗剂1可用于代谢研究[1]。

 名称

英文名 Ac-Arg-Cys-Met-5-aminopentanoyl-Arg-Val-Tyr-5-aminopentanoyl-Cys-NH2 trifluoroacetate salt (Disulfide bond)
英文别名 更多

 生物活性

描述 hMCH-1R拮抗剂1(化合物30)是具有3.6nM的KB值的人黑色素浓缩激素受体1(hMCHR1)的有效且选择性的拮抗剂。HMCH-1R拮抗剂1可以分别以65nM和49nM的IC50值与hMCHR1和hMCHR2结合。HMCH-1R拮抗剂1可用于代谢研究[1]。
相关类别
参考文献

[1]. Bednarek MA, et al. Synthesis and biological evaluation in vitro of selective, high affinity peptide antagonists of human melanin-concentrating hormone action at human melanin-concentrating hormone receptor 1. Biochemistry. 2002 May 21;41(20):6383-90.  

 物理化学性质

密度 1.4±0.1 g/cm3
分子式 C49H82N16O11S3
分子量 1167.471
精确质量 1166.551147
LogP -4.43
折射率 1.663

 英文别名

(4R,13S,16S,19S,28S,31R)-31-[(N2-Acetyl-L-arginyl)amino]-19-(3-carbamimidamidopropyl)-13-(4-hydroxybenzyl)-16-isopropyl-28-[2-(methylsulfanyl)ethyl]-6,12,15,18,21,27,30-heptaoxo-1,2-dithia-5,11,14,1 7,20,26,29-heptaazacyclodotriacontane-4-carboxamide
1,2-Dithia-5,11,14,17,20,26,29-heptaazacyclodotriacontane-4-carboxamide, 31-[[(2S)-2-(acetylamino)-5-[(aminoiminomethyl)amino]-1-oxopentyl]amino]-19-[3-[(aminoiminomethyl)amino]propyl]-13-[(4-hydroxyphenyl)methyl]-16-(1-methylethyl)-28-[2-(methylthio)ethyl]-6,12,15,18,21,27,30-heptaoxo-, (4R,13S,16S,19S,28S,31R)-