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Merck
CN

C5134

Sigma-Aldrich

2-氯腺苷

别名:

2-CADO, 2-氯腺嘌呤核苷

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About This Item

经验公式(希尔记法):
C10H12ClN5O4
CAS号:
分子量:
301.69
Beilstein:
43957
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

形式

powder

质量水平

SMILES字符串

Nc1nc(Cl)nc2n(cnc12)[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O

InChI

1S/C10H12ClN5O4/c11-10-14-7(12)4-8(15-10)16(2-13-4)9-6(19)5(18)3(1-17)20-9/h2-3,5-6,9,17-19H,1H2,(H2,12,14,15)/t3-,5-,6-,9-/m1/s1

InChI key

BIXYYZIIJIXVFW-UUOKFMHZSA-N

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应用

2-氯腺苷已用于:
  • 作为小鼠背侧海马体(DH)和腹侧海马体(VH)腺苷受体(A1R)的激动剂
  • 作为人工脑脊液(aCSF)组分,用于海马体切片的电生理实验
  • 作为固相萃取-液相色谱-串联质谱法(XLC-MS/MS)的内标,用于定量分析来自轴突裂解物和背根神经节(DRG)神经元的相应代谢物

生化/生理作用

2-氯腺苷是一种腺苷的类似物。它是腺苷A1受体激动剂。它可能具有抗氧化性能。

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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2-Chloroadenosine decreases long-term potentiation in the hippocampal CA1 area of the rat
de Mendoncca A and Ribeiro J A
Neuroscience Letters, 118(1), 107-111 (1990)
Effect of locally infused 2-chloroadenosine, an A1 receptor agonist, on spontaneous and evoked dopamine release in rat neostriatum
Ballarin M, et al.
Neuroscience Letters, 185(1), 29-32 (1995)
Sheila Weitzman et al.
Pediatric blood & cancer, 53(7), 1271-1276 (2009-09-05)
A prospective phase II Histiocyte Society study, LCH-S-98, evaluated the efficacy of 2-chlorodeoxyadenosine (2-CdA) monotherapy as salvage therapy in Langerhans cell histiocytosis (LCH). Patients with poor and intermediate risk LCH not responsive to initial therapy and patients with low-risk chronic
Javier Díaz-Alonso et al.
eLife, 9 (2020-08-25)
We tested the proposal that the C-terminal domain (CTD) of the AMPAR subunit GluA1 is required for LTP. We found that a knock-in mouse lacking the CTD of GluA1 expresses normal LTP and spatial memory, assayed by the Morris water
Menglong Zeng et al.
Neuron, 104(3), 529-543 (2019-09-08)
Transmembrane AMPA receptor (AMPAR) regulatory proteins (TARPs) modulate AMPAR synaptic trafficking and transmission via disc-large (DLG) subfamily of membrane-associated guanylate kinases (MAGUKs). Despite extensive studies, the molecular mechanism governing specific TARP/MAGUK interaction remains elusive. Using stargazin and PSD-95 as the

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