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Adenylyl Cyclase Activators

Cyclic Nucleotide Metabolism - cAMP
Cyclic nucleotides have been extensively studied as second messengers of intracellular events initiated by activation of many types of hormone and neurotransmitter receptors. Receptors that stimulate the conversion of ATP to cyclic 3′, 5′-adenosine monophosphate (cAMP) are associated with G-proteins. Binding of the hormone or neurotransmitter to its membrane-bound receptor induces a conformational change in the receptor that leads to activation of the α-subunit of the G-protein. The activated G subunit stimulates, while the non-activated G subunit inhibits adenylate cyclase (AC). Stimulation of AC catalyzes the conversion of cytoplasmic ATP to cAMP. cAMP activates cAMP-dependent protein kinases, including protein kinase A (PKA). By catalyzing the phosphorylation (activation or deactivation) of intracellular enzymes, cAMP-dependent kinases elicit a wide array of metabolic and functional processes. Negative regulation can occur in the pathway when phosphodiesterases (PDEs) catalyze the hydrolysis of cAMP to adenosine-5′-monophosphate (5′-AMP). Several families of phosphodiesterases (PDE I-V) act as regulatory switches by catalyzing the degradation of cAMP to 5′-AMP. PDE II is a low affinity PDE that can cleave both cAMP and cGMP. The activity of PDE II is stimulated by cGMP. PDE III is a low affinity PDE that is inhibited by cGMP and is involved in the regulation of smooth muscle and cardiac contraction. PDE IV is highly selective for cAMP and is the high affinity PDE present in most cell types.
References:
Francis, S.H., and Corbin, J.D., Cyclic nucleotide-dependent protein kinases: intracellular receptors for cAMP and cGMP action. Crit. Rev. Clin. Lab. Sci. 36, 275-328 (1999).
Juilfs, D.M., et al., Cyclic GMP as substrate and regulator of cyclic nucleotide phosphodiesterases (PDEs). Rev. Physiol. Biochem. Pharmacol. 135, 67-104 (1999).
Simonds, W.F., G protein regulation of adenylate cyclase. Trends Pharmacol. Sci. 20, 66-73 (1999).

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A0847 Adenylyl Cyclase Toxin from Bordetella pertussis ≥70% (SDS-PAGE), recombinant, expressed in E. coli, lyophilized powder, ≥50 units/mg protein
D3658 1,9-Dideoxyforskolin from Coleus forskohlii ≥97%, solid
F6886 Forskolin from Coleus forskohlii, ≥98% (HPLC), powder
SML0060 NB001 ≥98% (HPLC)
N3290 NKH 477 ≥98% (HPLC), powder
A1439 Pituitary adenylate cyclase activating polypeptide-38
A9808 Pituitary adenylate cyclase activating polypeptide-27 ovine ≥97% (HPLC), solid