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Merck
CN

O0766

Sigma-Aldrich

ONO-RS-082

≥97% (HPLC)

别名:

2-(p-Amylcinnamoyl)amino-4-chlorobenzoic acid, 4-Chloro-2-[[1-oxo-3-(4-pentylphenyl)-2-propen-1-yl]amino]-benzoic acid

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About This Item

经验公式(希尔记法):
C21H22ClNO3
CAS号:
分子量:
371.86
UNSPSC代码:
41106300
NACRES:
NA.77

质量水平

检测方案

≥97% (HPLC)

形式

powder

保质期

Do not freeze

储存条件

protect from light

颜色

white

溶解性

DMSO: ≥20 mg/mL

储存温度

room temp

InChI

1S/C21H22ClNO3/c1-2-3-4-5-15-6-8-16(9-7-15)10-13-20(24)23-19-14-17(22)11-12-18(19)21(25)26/h6-14H,2-5H2,1H3,(H,23,24)(H,25,26)/b13-10+

InChI key

MDVFITMPFHDRBZ-JLHYYAGUSA-N

生化/生理作用

ONO-RS-082 is a reversible phospholipase A2 inhibitor.

特点和优势

This compound is featured on the Phospholipase A2 page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

象形图

Environment

警示用语:

Warning

危险声明

预防措施声明

危险分类

Aquatic Acute 1 - Aquatic Chronic 1

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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M Fukunaga et al.
Experimental nephrology, 4(6), 340-349 (1996-11-01)
The phospholipase A2 inhibitors mepacrine, ONO-RS-082, and AACOCF3 completely inhibited prostaglandin E2 production induced by endothelin 1 in cultured rat mesangial cells, suggesting that phospholipase A2 is a critical enzyme in this process. TMB-8, an inhibitor of calcium mobilization from
H Nishino et al.
The American journal of physiology, 274(3 Pt 1), G525-G534 (1998-04-08)
We investigated the structural requirements for bombesin (BB)-like peptides to stimulate amylase secretion in rat pancreatic acini and examined the responsible intracellular signal transduction pathways. The tetradecapeptide BB-(1-14) was a full agonist, whereas the heptapeptide BB-(8-14) did not evoke amylase
T Takeuchi et al.
Japanese journal of pharmacology, 87(4), 309-317 (2002-02-07)
The origin of Ca2+ necessary for carbachol (CCh)-induced contraction of longitudinal muscle of the proximal colon of rats was studied. CCh induced contraction of the muscle consisting of two phases, phasic and tonic phases, with a concomitant biphasic increase in
Y Sugita et al.
European journal of pharmacology, 365(1), 77-89 (1999-02-13)
In order to examine some possibly misleading conclusions of the pharmacological analysis of the signal transduction pathways of gastric acid secretion, we evaluated various agents including inhibitors of protein kinase C, cyclic AMP-dependent protein kinase, phospholipase C, phospholipase A2, lipoxygenase
K L Byron
Circulation research, 78(5), 813-820 (1996-05-01)
[Arg8]-vasopressin (AVP) is both a potent vasoconstrictor and a mitogen for vascular smooth muscle cells. AVP binds to a single class of receptors (V1a) in the A7r5 rat aortic smooth muscle cell line (Kd approximately 2 nmol/L). Stimulation of these

商品

Phospholipase A2 (PLA2) enzymes hydrolyze glycerophospholipids, yielding arachidonic acid; inhibition targets eicosanoid biosynthesis.

磷脂酶A2(PLA2)代表的是一类可水解甘油磷脂的sn-2酯以产生脂肪酸和溶血磷脂的酶。目前已知的是,其中一些酶可在哺乳动物细胞中释放花生四烯酸以用于类花生酸的生物合成,因此PLA2抑制剂的开发引起了相当大的兴趣。基于氨基酸序列,现有超过12种不同的哺乳动物PLA2以及多种非哺乳动物的形式,它们被归类为具有多个亚组的14个组别。

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