CAS 159764-93-9

ADENOSINE 3',5'-CYCLIC MONOPHOSPHATE ACETOXYMETHYL ESTER

Description:

Adenosine 3',5'-cyclic monophosphate acetoxymethyl ester, commonly referred to as cAMP-AM, is a cell-permeable derivative of cyclic adenosine monophosphate (cAMP). This compound is characterized by its ability to mimic the action of cAMP within cells, facilitating the study of cAMP-dependent signaling pathways. It features an acetoxymethyl ester group that enhances its membrane permeability, allowing it to enter cells more easily than cAMP itself. Once inside the cell, esterases hydrolyze the acetoxymethyl group, releasing cAMP and activating downstream signaling cascades. cAMP is a crucial second messenger involved in various physiological processes, including regulation of metabolism, gene expression, and cell proliferation. The compound is often utilized in biochemical research to investigate the roles of cAMP in cellular functions and to explore potential therapeutic applications. Its CAS number, 159764-93-9, is a unique identifier that facilitates the cataloging and identification of this specific chemical substance in scientific literature and databases.

Formula: C₁₃H₁₆N₅O₈P

Synonyms:

• Adenosine-3’,5’-Cyclicmonophosphate,Acetoxymethylester(Camp-Am)
• Camp Am
• Adenosine-3',5'-Cylic Monophosphate,*Acetoxymethyl
• Adenosine-3',5'-cyclic monophosphoric acid acetoxymethyl ester

Adenosine 3′,5′-cyclic monophosphate acetoxymethyl ester

CAS: 159764-93-9

Formula: C₁₃H₁₆N₅O₈P

Molecular weight: 401.27

Ref: 7W-GK5767

Camp-am

CAS: 159764-93-9

Camp-am is a progestin contraceptive medication that prevents pregnancy by interfering with the ovulation process. It has been demonstrated to have a damaging effect on the genus Campylobacter, which can cause gastrointestinal illness. This drug is also known to modulate blood glucose levels and tumorigenicity in mice. Camp-am has been shown to activate horse melanocytes and increase hyperactivity in rats. Camp-am also induces glioma in mice, although it does not have any harmful effects on other cells in vitro. Camp-am has been shown to be activated by reperfusion following treatment with hydrogen peroxide or lipid peroxidation inhibitors, but not by a variety of other agents such as light, heat, or oxygen radicals.

Formula: C₁₃H₁₆N₅O₈P

Purity: Min. 95%

Molecular weight: 401.27 g/mol

Ref: 3D-JGA76493