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Merck
CN

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
UNSPSC Code:
41106305
PubChem Substance ID:
NACRES:
NA.77
MDL number:
Assay:
≥98% (HPLC)
Form:
powder
Quality level:
Storage condition:
desiccated
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产品名称

Rp-腺苷 3′,5′-环状单硫代磷酸酯 三乙铵盐, powder, ≥98% (HPLC)

Quality Level

assay

≥98% (HPLC)

form

powder

storage condition

desiccated

color

white to beige

solubility

H2O: 10 mg/mL

λmax

258 nm

storage temp.

−20°C

SMILES string

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

Application

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。

Biochem/physiol Actions

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。

Features and Benefits

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。

Disclaimer

非常吸湿。储存于干燥处。


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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商品

Cyclic nucleotides like cAMP modulate cell function via PKA activation and ion channels.


Shaomin Peng et al.
Investigative ophthalmology & visual science, 51(6), 3216-3225 (2010-01-01)
Bevacizumab and ranibizumab are currently used to treat age-related macular degeneration by neutralizing vascular endothelial growth factor (VEGF). In this study, the potential side effects on the outer blood-retinal barrier were examined. Human fetal RPE (hfRPE) cells were used because
J D Rothermel et al.
The Journal of biological chemistry, 259(13), 8151-8155 (1984-07-10)
The ability of the Rp diastereomer of adenosine cyclic 3',5'-phosphorothioate (Rp cAMPS) to inhibit glucagon-induced glycogenolysis was studied in hepatocytes isolated from fed rats. Preincubation of the cells for 20 min with progressively higher concentrations of Rp cAMPS followed by
L Y Wang et al.
Science (New York, N.Y.), 253(5024), 1132-1135 (1991-09-06)
In the mammalian central nervous system, receptors for excitatory amino acid neurotransmitters such as the alpha-amino-3-hydroxy-5-methyl-4- isoxazolepropionic acid (AMPA)-kainate receptor mediate a large fraction of excitatory transmission. Currents induced by activation of the AMPA-kainate receptor were potentiated by agents that



全球贸易项目编号

货号GTIN
A165-1MG04061833342626
A165-10MG04061832895598
A165-5MG04061832895604