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Merck
CN

C7938

Sigma-Aldrich

2-氯-N6-环戊基腺苷

adenosine receptor agonist

别名:

CCPA

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About This Item

经验公式(希尔记法):
C15H20ClN5O4
CAS号:
分子量:
369.80
MDL编号:
UNSPSC代码:
41106305
PubChem化学物质编号:
NACRES:
NA.51

质量水平

方案

≥98% (TLC)

表单

powder

溶解性

methanol: 19.60-20.40 mg/mL, clear, colorless to faintly yellow

储存温度

2-8°C

SMILES字符串

OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(NC4CCCC4)nc(Cl)nc23

InChI

1S/C15H20ClN5O4/c16-15-19-12(18-7-3-1-2-4-7)9-13(20-15)21(6-17-9)14-11(24)10(23)8(5-22)25-14/h6-8,10-11,14,22-24H,1-5H2,(H,18,19,20)/t8-,10-,11-,14-/m1/s1

InChI key

XSMYYYQVWPZWIZ-IDTAVKCVSA-N

应用

2-氯-N6-环戊基腺苷(CCPA)是一种具有高选择性的A1腺苷受体激动剂。CCPA通常与其他腺苷受体激动剂和拮抗剂一起使用,以平衡A(1)、A(2A)和A(3)受体的功能。这些药物包括DPCPX(A(1) 受体拮抗剂)、4-(2-[7-氨基-2-(2-呋喃基)[1,2,4]三唑[2,3-α][1,3,5]三嗪-5-基氨基]乙基)苯酚(A(2A)受体拮抗剂)和4-[2-[[6-氨基-9-(N-乙基-β-D-核呋喃核糖酰胺基)-9H-嘌呤-2-基]氨基]乙基]苯丙酸盐酸盐(A(2A) 受体激动剂)和Cl-IB-MECA(A(3)受体激动剂)。

生化/生理作用

具有高选择性的A1腺苷受体激动剂:据报道,A1受体的选择性是A2受体的10,000倍。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

N L D Smith et al.
Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases, 20(8), O480-O488 (2013-11-28)
Chronic cavitary pulmonary aspergillosis (CCPA) is a progressive lung condition with a 10-30% annual mortality. Although overtly immunocompetent, some immunogenetic defect in patients is likely. To investigate a possible immunogenetic defect in CCPA, we analysed biologically plausible candidate genes in
Romeo Romagnoli et al.
Journal of medicinal chemistry, 51(18), 5875-5879 (2008-08-30)
The synthesis and evaluation of a series of 2-amino-3-(4-chlorobenzoyl)-4-[4-(alkyl/aryl)piperazin-yl]thiophene derivatives as allosteric enhancers of the A 1-adenosine receptor are described. The nature of substituents on the phenyl ring tethered to the piperazine seem to exert a fundamental influence on the
Ruzanna Shkhyan et al.
Journal of molecular medicine (Berlin, Germany), 96(10), 1049-1060 (2018-08-09)
Osteoarthritis (OA), the most common form of arthritis, is characterized by inflammation of joints and cartilage degradation leading to disability, discomfort, severe pain, inflammation, and stiffness of the joint. It has been shown that adenosine, a purine nucleoside composed of
Mary Clare Luca et al.
Clinical hemorheology and microcirculation, 49(1-4), 287-293 (2012-01-05)
Despite decades of research and thousands of experimental publications, acute preconditioning strategies have yet to be implemented in clinical practice. While some have attributed this to a failure of the experimental studies to mimic the clinical environment, others have suggested
Ellen V Langemeijer et al.
Purinergic signalling, 9(1), 91-100 (2012-10-12)
The concept of functional selectivity offers great potential for the development of drugs that selectively activate a specific intracellular signaling pathway. During the last few years, it has become possible to systematically analyse compound libraries on G protein-coupled receptors (GPCRs)

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