A2224
Adenosine 3′,5′-cyclic monophosphate acetoxymethyl ester
>97% (HPLC)
别名:
cAMP AM
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关于此项目
经验公式（希尔记法）:
C13H16N5O8P
化学文摘社编号:
分子量:
401.27
UNSPSC Code:
41106305
PubChem Substance ID:
MDL number:
InChI
1S/C13H16N5O8P/c1-6(19)22-5-24-27(21)23-2-7-10(26-27)9(20)13(25-7)18-4-17-8-11(14)15-3-16-12(8)18/h3-4,7,9-10,13,20H,2,5H2,1H3,(H2,14,15,16)/t7-,9-,10-,13-,27?/m1/s1
SMILES string
CC(=O)OCOP1(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O1)n3cnc4c(N)ncnc34
InChI key
USKCKKDBQFHVEK-OQEAWBJFSA-N
assay
>97% (HPLC)
form
solid
packaging
pkg of 1 μmol
storage temp.
−20°C
Biochem/physiol Actions
Membrane-permeable precursor of the second messenger cyclic AMP
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)
法规信息
新产品
此项目有
C Schultz et al.
The Journal of biological chemistry, 268(9), 6316-6322 (1993-03-25)
Acetoxymethyl esters of alkyl or aryl phosphates can be prepared by reacting their trialkylammonium or silver salts with acetoxymethyl bromide. Because acetoxymethyl esters are rapidly cleaved intracellularly, they facilitate the delivery of organophosphates into the cytoplasm without puncturing or disruption
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