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Merck
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文件

119137

Sigma-Aldrich

CGS 21680 hydrochloride

≥96% (HPLC), solid, adenosine A2A receptor agonist, Calbiochem®

别名:

腺苷A2A受体激动剂I,CGS 21680,盐酸盐, CGS-21680,CGS21680,3-(4-(2-((6-氨基-9-((2R,3R,4S,5S)-5-(乙基氨甲酰基)-3,4-二羟基四氢呋喃-2-基)-9H-嘌呤-2-基)氨基)乙基)苯基)丙酸

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About This Item

经验公式(希尔记法):
C23H29N7O6 · xHCl
分子量:
499.52 (free base basis)
分類程式碼代碼:
12352200
NACRES:
NA.77

product name

腺苷A2A受体激动剂I,CGS 21680,盐酸盐,

化驗

≥96% (HPLC)

品質等級

形狀

solid

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
protect from light

顏色

white

溶解度

DMSO: 100 mM

運輸包裝

ambient

儲存溫度

−20°C

InChI

1S/C23H29N7O6/c1-2-25-21(35)18-16(33)17(34)22(36-18)30-11-27-15-19(24)28-23(29-20(15)30)26-10-9-13-5-3-12(4-6-13)7-8-14(31)32/h3-6,11,16-18,22,33-34H,2,7-10H2,1H3,(H,25,35)(H,31,32)(H3,24,26,28,29)/t16-,17+,18-,22?/m0/s1

InChI 密鑰

PAOANWZGLPPROA-OFRRTHGGSA-N

一般說明

CGS 21680 is a potent adenosine A2A receptors agonist (Ki = 27 nM) and xanthin derivative. CGS 21680 HCl exhibits reduced affinity for A2B receptors (Ki = 67 nM), but offers greater selectivity over A1R (Ki = 290 nM) and A3R (88.8 µM). Exerts an anti-inflammatory effect during chronic inflammation and ameliorates the tissue damage associated with collagen-induced arthritis. Been, shown to reduce CCR7 Protein Expression in THP1 macrophages. Shown to delay the progressive deterioration of motor performance and prevent a reduction in brain weight in murine model of Huntington′s disease.

包裝

用惰性气体包装

警告

毒性:标准处理(A)

外觀

以盐酸盐形式提供。

重構

在复溶后,分装并冷冻保存(-20°C)。储备溶液在-20°C下可稳定保存至多3个月。

其他說明

The molecular weight of CGS 21680 Hydrochloride this compound is batch-specific due to variable water content. For batch-specific molecular weight information, please refer the vial label or the certificate of analysis. The provided molecular weight represents the baseline molecular weight without water.

法律資訊

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

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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Cinthia Rangel-Sandoval et al.
iScience, 27(5), 109681-109681 (2024-04-29)
Pannexins are large-pore ion channels expressed throughout the mammalian brain that participate in various neuropathologies; however, their physiological roles remain obscure. Here, we report that pannexin1 channels (Panx1) can be synaptically activated under physiological recording conditions in rodent acute hippocampal

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