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N6-环戊基腺苷酸

更新时间:2025-08-27 11:57:44

N6-环戊基腺苷酸结构式
N6-环戊基腺苷酸结构式
品牌特惠专场
常用名 N6-环戊基腺苷酸 英文名 N6-Cyclopentyladenosine
CAS号 41552-82-3 分子量 335.36
密度 1.78g/cm3 沸点 673.4ºC at 760 mmHg
分子式 C15H21N5O4 熔点 N/A
MSDS 美版 闪点 361.1ºC

 N6-环戊基腺苷酸用途


N6-Cyclopentyladenosine (CPA) 是一个选择性的腺苷A3 受体 (Adenosine A1 receptor)的激动剂,其对人A1、A2A 和 A3 受体的Ki 分别为 2.3 nM、790 nM 和 43 nM。

 N6-环戊基腺苷酸名称

中文名 N6-环戊基腺苷酸
英文名 (2R,3R,4S,5R)-2-(6-(Cyclopentylamino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
中文别名 N6-环戊基TYLADENOSINE
英文别名 更多

 N6-环戊基腺苷酸生物活性

描述 N6-Cyclopentyladenosine (CPA) 是一个选择性的腺苷A3 受体 (Adenosine A1 receptor)的激动剂,其对人A1、A2A 和 A3 受体的Ki 分别为 2.3 nM、790 nM 和 43 nM。
相关类别
靶点实验

Ki: 2.3 nM (A1), 790 nM (A2A), 43 nM(A3)[1].

参考文献

[1]. Klotz KN, et al. Adenosine receptors and their ligands. Naunyn Schmiedebergs Arch Pharmacol. 2000 Nov;362(4-5):382-91.

[2]. Soliño M, et al. Adenosine A1 receptor: A neuroprotective target in light induced retinal degeneration. PLoS One. 2018 Jun 18;13(6):e0198838.

 N6-环戊基腺苷酸物理化学性质

密度 1.78g/cm3
沸点 673.4ºC at 760 mmHg
分子式 C15H21N5O4
分子量 335.36
闪点 361.1ºC
精确质量 335.15900
PSA 125.55000
InChIKey SQMWSBKSHWARHU-SDBHATRESA-N
SMILES OCC1OC(n2cnc3c(NC4CCCC4)ncnc32)C(O)C1O
折射率 1.816
储存条件 2-8℃

 N6-环戊基腺苷酸安全信息

个人防护装备 Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
危险品运输编码 NONH for all modes of transport

 N6-环戊基腺苷酸合成线路

~79%

N6-环戊基腺苷酸结构式

N6-环戊基腺苷酸

41552-82-3

文献:Ottria, Roberta; Casati, Silvana; Baldoli, Erika; Maier, Jeanette A.M.; Ciuffreda, Pierangela Bioorganic and Medicinal Chemistry, 2010 , vol. 18, # 23 p. 8396 - 8402

~70%

N6-环戊基腺苷酸结构式

N6-环戊基腺苷酸

41552-82-3

文献:Vittori, Sauro; Lorenzen, Anna; Stannek, Christina; Costanzi, Stefano; Volpini, Rosaria; Ijzerman, Adriaan P.; Von Frijtag Drabbe Kunzel, Jakobien K.; Cristalli, Gloria Journal of Medicinal Chemistry, 2000 , vol. 43, # 2 p. 250 - 260

~85%

N6-环戊基腺苷酸结构式

N6-环戊基腺苷酸

41552-82-3

文献:Fletcher, Steven Tetrahedron Letters, 2010 , vol. 51, # 22 p. 2948 - 2950

~%

N6-环戊基腺苷酸结构式

N6-环戊基腺苷酸

41552-82-3

文献:Vittori, Sauro; Lorenzen, Anna; Stannek, Christina; Costanzi, Stefano; Volpini, Rosaria; Ijzerman, Adriaan P.; Von Frijtag Drabbe Kunzel, Jakobien K.; Cristalli, Gloria Journal of Medicinal Chemistry, 2000 , vol. 43, # 2 p. 250 - 260

~%

N6-环戊基腺苷酸结构式

N6-环戊基腺苷酸

41552-82-3

文献:Vittori, Sauro; Lorenzen, Anna; Stannek, Christina; Costanzi, Stefano; Volpini, Rosaria; Ijzerman, Adriaan P.; Von Frijtag Drabbe Kunzel, Jakobien K.; Cristalli, Gloria Journal of Medicinal Chemistry, 2000 , vol. 43, # 2 p. 250 - 260

~%

N6-环戊基腺苷酸结构式

N6-环戊基腺苷酸

41552-82-3

文献:Inotek Pharmaceuticals Corporation Patent: US2007/238694 A1, 2007 ; Location in patent: Page/Page column 130 ;

 N6-环戊基腺苷酸文献115

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The effect of pH and ion channel modulators on human placental arteries.

PLoS ONE 9(12) , e114405, (2014)

Chorionic plate arteries (CPA) are located at the maternofetal interface where they are able to respond to local metabolic changes. Unlike many other types of vasculature, the placenta lacks nervous c...

Acid-sensing ion channel 3 decreases phosphorylation of extracellular signal-regulated kinases and induces synoviocyte cell death by increasing intracellular calcium.

Arthritis. Res. Ther. 16(3) , R121, (2014)

Acid-sensing ion channel 3 (ASIC3) is expressed in synoviocytes, activated by decreases in pH, and reduces inflammation in animal models of inflammatory arthritis. The purpose of the current study was...

Chemoenzymatic Syntheses of Sialylated Oligosaccharides Containing C5-Modified Neuraminic Acids for Dual Inhibition of Hemagglutinins and Neuraminidases.

Chemistry 21 , 10903-12, (2015)

A fast chemoenzymatic synthesis of sialylated oligosaccharides containing C5-modified neuraminic acids is reported. Analogues of GM3 and GM2 ganglioside saccharidic portions where the acetyl group of ...

 N6-环戊基腺苷酸靶点实验

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实验名称:Selectivity, ratio of affinity towards adenosine A3 to A2A
来源:ChEMBL
靶标:N/A
External Id:CHEMBL838353
实验名称:Selectivity, ratio of affinity towards adenosine A3 to A1
来源:ChEMBL
靶标:N/A
External Id:CHEMBL838352
实验名称:Inhibition of neurosphere proliferation of mouse neural precursor cells by MTT assay
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1266185
实验名称:Selectivity, ratio of affinity towards adenosine A2A to A1
来源:ChEMBL
靶标:N/A
External Id:CHEMBL838351
实验名称:Primary qHTS assay for inhibitors of alpha-synuclein gene (SNCA) expression
来源:NCGC
External Id:SNCA-p-activity-luciferase
实验名称:Inhibition of Bacillus subtilis ErmC' methyltransferase
来源:ChEMBL
靶标:rRNA adenine N-6-methyltransferase
External Id:CHEMBL5259871
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:Binding affinity against Adenosine A2A receptor by using [3H]CGS-21680 as radioligand
来源:ChEMBL
靶标:Adenosine receptor A2a
External Id:CHEMBL647738
实验名称:Effective concentration against A2AR mediated P12 adenylatencyclase activity
来源:ChEMBL
靶标:N/A
External Id:CHEMBL642755
实验名称:Tocris HTS for Inhibitors of Aerobactin Synthetase lucA
来源:23265
External Id:IucA Pilot Assay Tocris Library
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 N6-环戊基腺苷酸英文别名

N6-Cyclopentyladenosine
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