前往化源商城

353487-64-6

353487-64-6结构式
353487-64-6结构式

化源商城直购

英文名 Ac-Arg-Cys-Met-5-aminopentanoyl-Arg-Val-Tyr-5-aminopentanoyl-Cys-NH2 trifluoroacetate salt (Disulfide bond)
英文别名 AC-G-CYS-MET-5-AMINOPENTANOYL-G-VAL-TYR-5-AMINOPENTANOYL-CYS-NH2, (DISULFIDE BOND) TRIFLUOROACETATE
(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
Ac-g-Cys-Met-Ava-g-Val-Tyr-Ava-Cys-NH2|(Disulfide bond)
Ac-g-Cys-Met-5-aminopentanoyl-g-Val-Tyr-5-aminopentanoyl-Cys-NH2, (Disulfide bond)
L-Cysteinamide, N2-acetyl-L-ginyl-L-cysteinyl-L-methionyl-5-aminopentanoyl-L-ginyl-L-valyl-L-tyrosyl-5-aminopentanoyl-, cyclic (2→9)-disulfide
Ac-g-Cys-Met-5-aminopentanoyl-g-Val-Tyr-5-aminopentanoyl-Cys-NH2 trifluoroacetate salt (Disulfide bond)
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.  

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
本网页内容来自不同专业数据源,如对内容有疑义,欢迎联系service1@chemsrc.com。