A165
Rp-腺苷 3′，5′-环状单硫代磷酸酯 三乙铵盐
≥98% (HPLC), cAMP antagonist, powder
别名:
Rp-cAMPS 三乙铵盐, Rp-环状 3′，5′-氢硫代磷酸酯腺苷 三乙铵盐
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关于此项目
经验公式（希尔记法）:
C10H11N5O5PS · C6H16N
化学文摘社编号:
分子量:
446.46
MDL编号:
UNSPSC代码:
41106305
PubChem化学物质编号:
NACRES:
NA.77
产品名称
Rp-腺苷 3′，5′-环状单硫代磷酸酯 三乙铵盐, powder, ≥98% (HPLC)
方案
≥98% (HPLC)
表单
powder
储存条件
desiccated
颜色
white to beige
溶解性
H2O: 10 mg/mL
λmax
258 nm
储存温度
−20°C
SMILES字符串
CCN(CC)CC.Nc1ncnc2n(cnc12)[C@@H]3O[C@@H]4COP(O)(=S)O[C@H]4[C@H]3O
InChI
1S/C10H12N5O5PS.C6H15N/c11-8-5-9(13-2-12-8)15(3-14-5)10-6(16)7-4(19-10)1-18-21(17,22)20-7;1-4-7(5-2)6-3/h2-4,6-7,10,16H,1H2,(H,17,22)(H2,11,12,13);4-6H2,1-3H3/t4-,6-,7-,10-,21?;/m1./s1
InChI key
OXIPZMKSNMRTIV-NVGWRVNNSA-N
相关类别
应用
Rp-腺苷-3′，5′-环一硫代磷酸三乙酯铵盐已被用作cAMP的拮抗剂，以阻断cAMP-PKA信号通路。
生化/生理作用
Rp-腺苷-3′，5′-环一硫代磷酸三乙酯铵盐能够抑制蛋白激酶A（PKA）。
腺苷-3′，5′-环状单硫代磷酸酯 Rp-非对映异构体。cAMP（cAMP 依赖性蛋白激酶I 和 II）激活作用的特异性膜渗透性抑制剂；对环核苷酸磷酸二酯酶具有抗性；在许多系统中阻断 cAMP 介导的作用。
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。
免责声明
非常吸湿。储存于干燥处。
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
Olav A Gressner et al.
Liver international : official journal of the International Association for the Study of the Liver, 29(6), 886-897 (2009-03-18)
Recently, we identified hepatocytes as the major cellular source of profibrogenic connective tissue growth factor (CTGF/CCN2) in the liver. Based on reports of a hepatoprotective effect of coffee consumption, we were the first to provide evidence that caffeine suppresses transforming
cAMP analog antagonists of cAMP action.
L H Botelho et al.
Methods in enzymology, 159, 159-172 (1988-01-01)
Qingqing Zhu et al.
Journal of cellular and molecular medicine, 26(14), 3816-3827 (2022-06-10)
Radix puerariae, a traditional Chinese herbal medication, has been used to treat patients with diabetic kidney disease (DKD). Our previous studies demonstrated that puerarin, the active compound of radix puerariae, improves podocyte injury in type 1 DKD mice. However, the
Carmen Müllner et al.
The FEBS journal, 276(21), 6218-6226 (2009-09-22)
Besides being activated by G-protein beta/gamma subunits, G-protein activated potassium channels (GIRKs) are regulated by cAMP-dependent protein kinase. Back-phosphorylation experiments have revealed that the GIRK1 subunit is phosphorylated in vivo upon protein kinase A activation in Xenopus oocytes, whereas phosphorylation
Role of PLC-PIP2 and cAMP-PKA signal pathways in radiation-induced immune-suppressing effect
Dong JC, et al.
Biomedical and Environmental Sciences : Bes, 27(1), 27-34 (2014)
商品
Cyclic nucleotides like cAMP modulate cell function via PKA activation and ion channels.
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