N2,2'-O-DIBUTYRYLGUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SODIUM SALT

N2,2'-O-DIBUTYRYLGUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SODIUM SALT

中文名称N2,2'-O-DIBUTYRYLGUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SODIUM SALT
中文同义词化合物 T11038;二丁酰-CGMP 钠盐;化合物 DIBUTYRYL-CGMP SODIUM;DIBUTYRYL-CGMP,CGMP ANALOG
英文名称N2,2'-O-DIBUTYRYLGUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SODIUM SALT
英文同义词MGBPJXVWDGGLKI-GBIKJYCISA-M;dibutyryl cyclic 3',5'-guanosine monophosphate, sodium;N2,2μ-O-Dibutyrylguanosine 3μ,5μ-cyclic monophosphate hydrate sodium salt;Guanosine 3,5-cyclic Monophosphate, N2,2-O-Dibutyryl-, Sodium Salt - CAS 51116-00-8 - Calbiochem;N2,2μ-O-Dibutyrylguanosine 3μ,5μ-cyclic monophosphate dihydrate sodium salt;N,2'-O-Dibutyrylguanosine 3',5'-phosphoric acid;N2,2'-O-Dibutyryl cGMP;Dibutyryl-Cyclic GMP (sodium salt)
CAS号51116-00-8
分子式C18H24N5O9P.Na
分子量508.38
EINECS号2569922
相关类别Biochemicals and Reagents;Nucleosides, Nucleotides, Oligonucleotides;Nucleotide Analogs;Cyclic Nucleotide Metabolism;Cyclic Nucleotides and AnalogsSerine/Threonine Kinase Biology;G Proteins and Cyclic Nucleotides;Protein Kinase G (PKG);Serine/Threonine Kinase Activators
Mol文件51116-00-8.mol
结构式N2,2'-O-DIBUTYRYLGUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SODIUM SALT 结构式

N2,2'-O-DIBUTYRYLGUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SODIUM SALT 性质

储存条件−20°C
溶解度H2O:50 mg/mL
形态粉末
颜色米白色
InChIKeyMGBPJXVWDGGLKI-GBIKJYCISA-M
SMILES[Na+].[P]1(=O)(O[C@@H]2[C@H](O[C@H]([C@@H]2OC(=O)CCC)[n]3c4nc(nc(c4nc3)O)NC(=O)CCC)CO1)[O-]

N2,2'-O-DIBUTYRYLGUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SODIUM SALT 用途与合成方法

Dibutyryl-cGMP sodium (Bt2cGMP sodium) 是细胞可渗透的 cGMP 类似物,可优先激活 cGMP 依赖性蛋白激酶 (PKG)。Dibutyryl-cGMP sodium 抑制 γ 凝血酶刺激的人血小板中 [3H]-花生四烯酸的释放。Dibutyryl-cGMP sodium 可通过激活ATP 敏感的 K+ 通道而具有镇痛作用。

cGMP-dependent protein kinase (PKG);
ATP-sensitive K + channels

Dibutyryl-cGMP is able to induce process elongation and branching in astrocytes resulting from a rapid, reversible and concentration-dependent redistribution of glial fibrillary acidic protein (GFAP) and actin filaments without significant change in protein levels.
When cells are co-incubated with Dibutyryl-cGMP (100 μM) stress fibre formation is prevented and cells acquired a stellate morphology in cerebellar astrocytes.
In cells treated with Dibutyryl-cGMP (100 μM, 2 h) the particulate fraction is nearly devoid of RhoA protein. Dibutyryl-cGMP prevents RhoA-membrane association.
Using the scratchwound model, the size of the wound is significantly smaller in cells treated with Dibutyryl-cGMP after the wound indicating that dbcGMP accelerates wound closure.

Dibutyryl-cGMP (50-200 μg/paw; subcutaneous injection; male Wistar rats) treatment antagonizes the hyperalgesic effect of PGE2 in a dose-dependent manner. Maximal antinociceptive effect of DbcGMP is at 1 h after administration and last for plus 2 h.

Animal Model: Male Wistar rats (180- 250 g) injection with Prostaglandin E2 (PGE2)
Dosage: 50 μg/paw, 75 μg/paw, 100 μg/paw and 200 μg/paw
Administration: Subcutaneous injection
Result: Antagonized the hyperalgesic effect of PGE2 (2 μg/paw), in a dose-dependent manner.

安全信息

WGK Germany3
F10-21
存储类别11 - 可燃固体

MSDS信息

提供商 语言
英文
更新日期产品编号产品名称CAS号包装价格
2026/06/05HY-130354Dibutyryl-cGMP sodium51116-00-81 mg997元
2026/06/05HY-130354N2,2'-O-DIBUTYRYLGUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SODIUM SALT
Dibutyryl-cGMP sodium
51116-00-85mg2500元

N2,2'-O-DIBUTYRYLGUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SODIUM SALT 上下游产品信息

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