您好,欢迎来到化工原料网! [登录] [免费注册]
化工原料网
位置:首页 > 产品库 > Litorin(trifluoroacetate salt)
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
Litorin(trifluoroacetate salt)
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Litorin(trifluoroacetate salt)图片
包装与价格:
包装价格(元)
1mg电议
5mg电议
10mg电议

产品介绍
A peptide with diverse biological activities
Canonical SMILESO=C([C@H]1NC(CC1)=O)N[C@@H](CCC(N)=O)C(N[C@H](C(N[C@@H](C)C(N[C@@H](C(C)C)C(NCC(N[C@H](C(N[C@H](C(N[C@H](C(N)=O)CCSC)=O)CC2=CC=CC=C2)=O)CC3=CN=CN3)=O)=O)=O)=O)CC4=CNC5=CC=CC=C45)=O.OC(C(F)(F)F)=O
分子式C51H68N14O11S·XCF3COOH
分子量1085.2
溶解度Water: soluble
储存条件-20°C
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

Litorin is a peptide originally isolated fromL. aureathat has diverse biological activities.1,2,3,4It is an agonist of the gastrin-releasing peptide receptor (GRPR) and the neuromedin B (NMB) receptor in BALB/c 3T3 fibroblasts expressing the human receptors (EC50s = 0.44 and 0.03 nM, respectively) and binds to frog bombesin receptor subtype 4 (BB4) in CHO-K1 cells (Ki= 1.2 nM).2,3Litorin (10-100 ng/kg) induces contractions of isolated guinea pig gallbladder.4It decreases food intake in rats when administered at doses ranging from 4 to 128 µg/kg.1

1.Kulkosky, P.J., and Gibbs, J.Litorin suppresses food intake in ratsLife Sci.31(7)685-692(1982) 2.Uehara, H., GonzÁlez, N., Sancho, V., et al.Pharmacology and selectivity of various natural and synthetic bombesin related peptide agonists for human and rat bombesin receptors differsPeptides32(8)1685-1699(2011) 3.Katsuno, T., Pradhan, T.K., Ryan, R.R., et al.Pharmacology and cell biology of the bombesin receptor subtype 4 (BB4-R)Biochemistry38(22)7307-7320(1999) 4.Endean, R., Erspamer, V., Falconieri Erspamer, G., et al.Parallel bioassay of bombesin and litorin, a bombesin-like peptide from the skin of Litoria aureaBr. J. Pharmacol.55(2)213-219(1975)