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Merck

W102

Sigma-Aldrich

( R )-(+)-WIN 55,212-2 甲磺酸盐

≥98% (HPLC), powder, CB2 agonist

别名:

( R )-(+)-\ [2,3-二氢-5-甲基-3\ [(4-吗啉基)甲基] 吡咯并 \ [1,2,3-de]-1,4-苯并恶嗪基]-(1-萘基)甲酮 甲磺酸盐, WIN 55212-2 甲磺酸酯, WIN 552122 甲磺酸酯

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About This Item

线性分子式:
C27H26N2O3 · CH3SO3H
分子量:
522.61
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

product name

( R )-(+)-WIN 55,212-2 甲磺酸盐, ≥98% (HPLC)

品質等級

化驗

≥98% (HPLC)

形狀

powder

藥物控制

regulated under CDSA - not available from Sigma-Aldrich Canada

顏色

white to beige

溶解度

0.1 M HCl: 0.25 mg/mL
DMSO: 12 mg/mL
45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: 2.4 mg/mL
0.1 M NaOH: insoluble
H2O: insoluble

SMILES 字串

CS(O)(=O)=O.Cc1c(C(=O)c2cccc3ccccc23)c4cccc5OC[C@@H](CN6CCOCC6)n1c45

InChI

1S/C27H26N2O3.CH4O3S/c1-18-25(27(30)22-9-4-7-19-6-2-3-8-21(19)22)23-10-5-11-24-26(23)29(18)20(17-32-24)16-28-12-14-31-15-13-28;1-5(2,3)4/h2-11,20H,12-17H2,1H3;1H3,(H,2,3,4)/t20-;/m1./s1

InChI 密鑰

FSGCSTPOPBJYSX-VEIFNGETSA-N

基因資訊

一般說明

WIN 55,212-2 是氨基烷基吲哚类化合物的成员。

應用

(R)-(+)-WIN 55,212-2 甲磺酸盐已被用作高亲和力大麻素激动剂,腹腔注射到大鼠体内诱导行为敏化。它还被用作合成大麻素药物和大麻素受体 1 (CNR1) 激动剂,治疗 Becn2 +/-小鼠和野生型 (WT) 同窝出生小鼠,分析大脑中 CNR1 的水平。

生化/生理作用

已知其可减少脂多糖介导的肿瘤坏死因子-α 的释放和小鼠的白细胞介素-1。

特點和優勢

《受体分类和信号转导》手册的 GABAC受体页有该化合物的介绍。想要浏览手册的其他页面, 请单击此处

法律資訊

经 Sterling-Winthrop,Inc. 许可销售。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

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访问文档库

Dual Role of PPAR-c in Induction and Expression of Behavioral Sensitization to Cannabinoid Receptor Agonist WIN55,212-2
Enayatfard L, et al.
Neuromolecular Medicine, 15, 523-535 (2013)
Rational design and synthesis of an orally active indolopyridone as a novel conformationally constrained cannabinoid ligand possessing antiinflammatory properties
Wrobleski ST, et al.
Journal of Medicinal Chemistry, 46(11), 2110-2116 (2003)
U Herzberg et al.
Neuroscience letters, 221(2-3), 157-160 (1997-01-17)
The effects of a high affinity cannabinoid receptor agonist were evaluated in rats subjected to chronic constriction injury of the sciatic nerve (CCI) or a sham operation. Intraperitoneal (i.p.) injections of the active, but not the inactive enantiomer, alleviated the
Autophagy activation by novel inducers prevents BECN2-mediated drug tolerance to cannabinoids
Kuramoto K, et al.
Autophagy, 12(9), 1460-1471 (2016)
Gaëtan Philippot et al.
Toxicological sciences : an official journal of the Society of Toxicology, 166(1), 203-212 (2018-08-31)
Acetaminophen (AAP; also known as paracetamol) is the most used and only recommended analgesic and antipyretic among pregnant women and young children. However, recent findings in both humans and rodents suggest a link between developmental exposure to AAP and adverse

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