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Irsogladine
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。
Irsogladine图片
CAS NO:57381-26-7
包装与价格：
包装价格(元)
10mM (in 1mL DMSO)电议
50mg电议

产品介绍
Irsogladine 是一种 PDE4 抑制剂和毒蕈碱乙酰胆碱受体结合剂。
Cas No.57381-26-7
别名伊索拉定; Dicloguamine
化学名6-(2,5-dichlorophenyl)-1,3,5-triazine-2,4-diamine
Canonical SMILESC1=CC(=C(C=C1Cl)C2=NC(=NC(=N2)N)N)Cl
分子式C9H7Cl2N5
分子量256.09
溶解度≥ 12.8mg/mL in DMSO
储存条件Store at -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

Irsogladine is a PDE4 inhibitor and muscarinic acetylcholine receptor binder.Target: PDE4; mACHRIrsogladine treatment (300 and 500 mg/kg/day) resulted in a dose-dependent reduction of angiogenesis in wild-type mice by 21 and 45.3% (P< 0.02, P< 0.001), in tPA-deficient mice by 42.6 and 46% (P< 0.001, P< 0.001), and in uPA-deficient mice by 27.2 and 46% (P< 0.05, p< 0.001), respectively. Irsogladine inhibits bFGF-induced angiogenesis in wild-type, tPA-knockout, and uPA-knockout mice [1]. Irsogladine up-regulates GJIC between PC cells via regulation of the PKA pathway. It also suggests a useful adjuvant of Irsogladine to pancreatic cancer therapy [2]. irsogladine produces the increase of intracellular cAMP content via non-selective inhibition of PDE isozymes, which may be a key mechanism involved in its gastroprotective actions [3].

References:
[1]. Ren, C.J., et al., Irsogladine maleate inhibits angiogenesis in wild-type and plasminogen activator-deficient mice. J Surg Res, 1998. 77(2): p. 126-31.
[2]. Kawasaki, Y., et al., Irsogladine malate up-regulates gap junctional intercellular communication between pancreatic cancer cells via PKA pathway. Pancreas, 2002. 25(4): p. 373-7.
[3]. Kyoi, T., et al., Phosphodiesterase inhibition by a gastroprotective agent irsogladine: preferential blockade of cAMP hydrolysis. Life Sci, 2004. 75(15): p. 1833-42.