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ChemicalBook--->CAS DataBase List--->71774-13-5

71774-13-5

71774-13-5 Structure

71774-13-5 Structure
IdentificationBack Directory
[Name]

ADENOSINE-3',5'-CYCLIC -MONOPHOSPHOROTHIOATE
[CAS]

71774-13-5
[Synonyms]

cAMPS-Sp
(S)-Adenosine
Triethylammoniumsalt
camps,sp-isomer,teasalt
ADENOSINE-3',5'-CYCLIC -MONOPHOSPHOROTHIOATE
Adenosine, cyclic 3',5'-[hydrogen (S)-phosphorothioate]
Adenosine-3'',5''-cyclic monophosphothioate sodium salt Sp isomer
(S)-ADENOSINE, CYCLIC 3',5'-(HYDROGENPHOSPHOROTHIOATE) TRIETHYLAMMONIUM
adenosine-3’,5’-cyclicmonophosphorothioate,sp-isomer(sp-camps),sodiumsalt
ADENOSINE3,5-CYCLICMONOPHOSPHOTHIOATESP-ISOMERTRIETHYLAMMONIUMSALT,HIGHPURITY
[Molecular Formula]

C10H12N5O5PS
[MDL Number]

MFCD01459901
[MOL File]

71774-13-5.mol
[Molecular Weight]

345.27
Chemical PropertiesBack Directory
[Boiling point ]

648.0±65.0 °C(predicted)
[density ]

2.38±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)
[storage temp. ]

Desiccate at -20°C
[pka]

-0.55±0.60(predicted)
Hazard InformationBack Directory
[Uses]

(S)-Adenosine, cyclic 3'',5''-(hydrogenphosphorothioate) triethylammonium is an activator of PKA.
[Definition]

ChEBI: (Sp)-cAMPS is a nucleoside 3',5'-cyclic phosphorothioate having adenine as the nucleobase (the Sp-stereoisomer). It has a role as a protein kinase agonist. It is a member of purines and a nucleoside 3',5'-cyclic phosphorothioate. It is functionally related to a 3',5'-cyclic AMP.
[Biological Activity]

Cell-permeable cAMP analog that activates cAMP receptor proteins such as PKA and cAMP-regulated guanine nucleotide exchange factor.
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