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Merck
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重要文件

O0766

Sigma-Aldrich

ONO-RS-082

≥97% (HPLC)

同義詞:

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

經驗公式(希爾表示法):
C21H22ClNO3
CAS號碼:
分子量::
371.86
分類程式碼代碼:
41106300
NACRES:
NA.77
暫時無法取得訂價和供貨情況

品質等級

化驗

≥97% (HPLC)

形狀

powder

儲存期限

Do not freeze

儲存條件

protect from light

顏色

white

溶解度

DMSO: ≥20 mg/mL

儲存溫度

room temp

SMILES 字串

Clc1cc(c(cc1)C(=O)O)NC(=O)\C=C\c2ccc(cc2)CCCCC

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 密鑰

MDVFITMPFHDRBZ-JLHYYAGUSA-N

生化/生理作用

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

特點和優勢

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.

象形圖

Environment

訊號詞

Warning

危險聲明

防範說明

危險分類

Aquatic Acute 1 - Aquatic Chronic 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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分析證明 (COA)

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Rania Abu-Hamdah et al.
Cell biology international, 28(1), 7-17 (2004-02-05)
Aquaporins (AQP) are involved in rapid and active gating of water across biological membranes. The molecular regulation of AQP is unknown. Here we report the isolation, identification and reconstitution of the regulatory complex of AQP-1. AQP-1 and Galphai3 have been
Y Li et al.
American journal of physiology. Heart and circulatory physiology, 280(6), H2658-H2664 (2001-05-18)
Physiological concentrations of [Arg(8)]vasopressin (AVP; 10-500 pM) stimulate oscillations of cytosolic free Ca2+ concentration (Ca2+ spikes) in A7r5 vascular smooth muscle cells. We previously reported that this effect of AVP was blocked by a putative phospholipase A2 (PLA2) inhibitor, ONO-RS-082
H Yoshida et al.
The American journal of physiology, 273(3 Pt 1), G735-G747 (1997-10-08)
In an attempt to examine the structure-activity relationship of the cholecystokinin (CCK) peptide, we examined the structural motif of CCK truncated peptides responsible for rat pancreatic acinar amylase secretion and signal transduction. CCK-6 (Met28-Gly29-Trp30-Met31-Asp32-Phe33 -NH2), CCK-5 [CCK-(29-33)], and CCK-4 [CCK-(30-33)]
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

文章

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。

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

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