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Merck
CN

C5438

8-（4-氯苯硫基）-鸟苷 3′,5′-环单磷酸 钠盐

≥95% (HPLC), cGMP dependent protein kinase (PKG) activator, powder

别名:

8-pCPT-cGMP, pCPT-cGMP

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关于此项目

经验公式（希尔记法）:
C16H14ClN5NaO7PS
化学文摘社编号:
51239-26-0
分子量:
509.79
UNSPSC Code:
41106305
PubChem Substance ID:
24892786
NACRES:
NA.77
MDL number:
MFCD00674888

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产品名称

8-（4-氯苯硫基）-鸟苷 3′,5′-环单磷酸 钠盐, ≥95% (HPLC), powder

color

white

SMILES string

[Na+].NC1=Nc2c(nc(Sc3ccc(Cl)cc3)n2[C@@H]4O[C@@H]5COP([O-])(=O)O[C@H]5[C@H]4O)C(=O)N1

InChI

1S/C16H15ClN5O7PS.Na/c17-6-1-3-7(4-2-6)31-16-19-9-12(20-15(18)21-13(9)24)22(16)14-10(23)11-8(28-14)5-27-30(25,26)29-11;/h1-4,8,10-11,14,23H,5H2,(H,25,26)(H3,18,20,21,24);/q;+1/p-1/t8-,10-,11-,14-;/m1./s1

InChI key

REEQGIQRCDWDRA-ZBMQJGODSA-M

assay

≥95% (HPLC)

form

powder

solubility

H2O: 25 mg/mL

storage temp.

−20°C

Quality Level

200

相关类别

Application

8-（4-氯苯硫基）-鸟苷 3′,5‘-环状单磷酸钠盐已被用于激活血管平滑肌细胞（VSMC）中的GMP依赖性蛋白激酶（PKG）。

Biochem/physiol Actions

cGMP的膜渗透性类似物，不影响cGMP调节的磷酸二酯酶。 比8-Br-cGMP更有效的cGMP类似物，因为它具有更高的膜渗透性和更高的抗磷酸二酯酶水解能力。用作cGMP依赖性蛋白激酶（PKG）的选择性激活剂。被发现是一种非常有效的环状核苷酸门控通道激动剂。

Features and Benefits

《受体分类和信号转导》手册的PKA & PKG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。
这种化合物是环核苷酸研究的特色产品。点击此处发现更多特色环核苷酸产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000512518
0000512518
0000462973
0000462973
0000353336

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Yang Chen et al.
Circulation research, 124(10), 1462-1472 (2019-04-02)
Acute kidney injury (AKI) has a high prevalence and mortality in critically ill patients. It is also a powerful risk factor for heart failure incidence driven by hemodynamic changes and neurohormonal activation. However, no drugs have been approved by the
J Y Wei et al.
Journal of molecular neuroscience : MN, 10(1), 53-64 (1998-05-20)
Cyclic nucleotide-gated (CNG) channels are expressed in many cell types in both the nervous system and nonexcitable tissues. In order to understand the roles of cGMP-gated channels, and to distinguish actions of cGMP mediated through CNG channels from those through
B E VanUffelen et al.
Biochemical pharmacology, 56(8), 1061-1063 (1998-10-17)
In previous experiments, it was shown that migration of electropermeabilized human neutrophils induced by a combination of cGMP and cAMP markedly lower relative to that induced by cGMP or cAMP alone. However, when cGMP was replaced with 8-(para-chlorophenylthio-guanosine-3',5'-cyclic monophosphate (8-pCPT-cGMP)
P He et al.
The American journal of physiology, 274(6 Pt 2), H1865-H1874 (1998-06-25)
To investigate the mechanisms whereby guanosine 3',5'-cyclic monophosphate (cGMP) modulates microvessel permeability in vivo, we measured changes in microvessel hydraulic conductivity (Lp) and endothelial cytoplasmic Ca2+ concentration ([Ca2+]i) in response to the cGMP analogs 8-bromo-cGMP (8-BrcGMP) and 8-(p-chlorophenylthio)cGMP (8-pCPT-cGMP) in
M Suhasini et al.
Molecular and cellular biology, 18(12), 6983-6994 (1998-11-20)
Agents which increase the intracellular cyclic GMP (cGMP) concentration and cGMP analogs inhibit cell growth in several different cell types, but it is not known which of the intracellular target proteins of cGMP is (are) responsible for the growth-suppressive effects
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