B1381
8-溴鸟嘌呤3′,5′-环一磷酸 钠盐
≥98% (HPLC), powder
别名:
8-Br-cGMP, 8-溴-环 GMP
质量水平
方案
≥98% (HPLC)
表单
powder
溶解性
H2O: 50 mg/mL
储存温度
−20°C
SMILES字符串
[Na+].NC1=Nc2c(nc(Br)n2[C@@H]3O[C@@H]4COP([O-])(=O)O[C@H]4[C@H]3O)C(=O)N1
InChI
1S/C10H11BrN5O7P.Na/c11-9-13-3-6(14-10(12)15-7(3)18)16(9)8-4(17)5-2(22-8)1-21-24(19,20)23-5;/h2,4-5,8,17H,1H2,(H,19,20)(H3,12,14,15,18);/q;+1/p-1/t2-,4-,5-,8-;/m1./s1
InChI key
ZJRFCXHKYQVNFK-YEOHUATISA-M
一般描述
8-溴鸟苷水合物3′,5′-环磷酸腺苷是环鸟苷酸3′:5′-单磷酸(cGMP)的细胞可透过性cGMP类似物。它是一种脂溶性类似物,用于基于cGMP的心肌细胞收缩研究。
应用
使用8-溴鸟苷水合物3′,5′-环磷酸钠盐:
- 作为环鸟苷酸3′:5′-单磷酸(cGMP)激动剂用于视网膜神经节轴突塌陷测定(10)
- 作为反应缓冲液的组成部分,用于重组蛋白激酶的体外激酶活性测定(PKG)(11)
- 作为环核苷酸类似物,用于诱导人胚肾细胞中环化核苷酸门控通道(CNGA和CNGC)表达(12)
生化/生理作用
与cGMP相比,8-溴鸟苷水合物3′,5′-环磷酸腺苷对磷酸二酯酶的水解作用具有更强的抵抗性。激活cGMP依赖性蛋白激酶。它减缓或抑制气管平滑肌细胞内钙振荡对乙酰胆碱的反应。8-溴鸟苷水合物3′,5′-环磷酸钠盐模仿一氧化氮生成药物的效果。它调节生物周期节律,增加视网膜神经脉冲。眼内8-溴鸟苷水合物3′,5′--环磷酸腺苷可能有利于非-R-型光受体的转导。
细胞渗透性 cGMP 类似物比 cGMP 对磷酸二酯酶水解有更大的抵抗力。激活 cGMP 依赖性蛋白激酶。减缓或抑制乙酰胆碱引起的气管平滑肌细胞内钙振荡。据报告,其可模拟一氧化氮生成药物的作用。
特点和优势
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。
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
Cyclic guanosine 3': 5'-monophosphate mimics the effects of light on a circadian pacemaker in the eye of aplysia
Eskin A, et al.
The Journal of Neuroscience, 4(10), 2466-2471 (1984)
8-bromo-cGMP reduces the myofilament response to Ca2+ in intact cardiac myocytes.
Shah AM, et al.
Circulation Research, 74(5), 970-978 (1994)
U C Garg et al.
The Journal of clinical investigation, 83(5), 1774-1777 (1989-05-01)
Endothelium-derived relaxing factor has been recently identified as nitric oxide. The purpose of this study was to determine if vasodilator drugs that generate nitric oxide inhibit vascular smooth muscle mitogenesis and proliferation in culture. Three chemically dissimilar vasodilators, sodium nitroprusside
Arun Govindapillai et al.
Scientific reports, 8(1), 6939-6939 (2018-05-04)
Patients born with congenital heart defects frequently encounter arrhythmias due to defects in the ventricular conduction system (VCS) development. Although recent studies identified transcriptional networks essential for the heart development, there is scant information on the mechanisms regulating VCS development.
Birgit Houweling et al.
Experimental biology and medicine (Maywood, N.J.), 237(2), 201-210 (2012-02-09)
Cardiovascular disease is characterized by impaired exercise capacity and endothelial dysfunction, i.e. reduced bioavailability of nitric oxide (NO). Phosphodiesterase-5 (PDE5) inhibition is a promising vasodilator therapy, but its effects on pulmonary and systemic hemodynamic responses to exercise in the absence
商品
Cyclic nucleotides like cAMP modulate cell function via PKA activation and ion channels.
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