cAMP
cAMP (cyclic adenosine monophosphate) is a second messenger used for intracellular signal transduction in many different organisms, conveying the cAMP-dependent pathway.
Products for cAMP
- Cat.No. Product Name Information
- GC48920 β-Carboline-1-carboxylic Acid An alkaloid with diverse biological activities
- GC46554 2'-O-Monosuccinyladenosine-3',5'-cyclic monophosphate 2'-O-Monosuccinyladenosine-3',5'-cyclic monophosphate is a cAMP analog that can be covalently coupled to acetylcholinesterase.
- GC48381 5'-pApA (sodium salt) A linearized form of cyclic di-AMP
- GC41423 5-trans Prostaglandin E2 5-trans PGE2 occurs naturally in some gorgonian corals and is a common impurity in commercial lots of PGE1.
- GC12834 6-Bnz-cAMP sodium salt cAMP analog,PKA activator
-
GC42616
7-oxo Staurosporine
7-oxo Staurosporine is an antibiotic originally isolated from S.
- GC16929 8-Bromo-cAMP, sodium salt Cell-permeable cAMP analog that activates PKA
- GC42622 8-bromo-Cyclic AMP 8-bromo-Cyclic AMP is a brominated derivative of cAMP that remains long-acting due to its resistance to degradation by cAMP phosphodiesterase.
- GC49285 Adenosine 5’-methylenediphosphate (hydrate) An inhibitor of ecto-5’-nucleotidase
- GC10941 cAMPS-Rp, triethylammonium salt cAMPS-Rp, triethylammonium salt, a cAMP analog, is a potent, competitive cAMP-induced activation of cAMP-dependent PKA I and II (Kis of 12.5 μM and 4.5 μM, respectively) antagonist.
- GC12706 cAMPS-Sp, triethylammonium salt cAMPS-Sp, triethylammonium salt, a cAMP analog, is a potent, competitive cAMP-induced activation of cAMP-dependent PKA I and II (Kis of 12.5 μM and 4.5 μM, respectively) antagonist.
- GC47088 Cilostazol-d4 An internal standard for the quantification of cilostazol
- GC43339 Cyclic di-AMP (sodium salt) Cyclic di-AMP (c-di-AMP) is a second messenger produced by bacteria but not by mammals.
-
GC43341
Cyclic GMP
Guanosine 3',5'-cyclic monophosphate (cyclic GMP or cGMP) is a second messenger that is biosynthesized from GTP by guanylate cyclases.
- GC12824 Dibutyryl-cAMP, sodium salt Dibutyryl-cAMP, sodium salt salt (Dibutyryl-cAMP sodium salt) is a stabilized cyclic AMP (cAMP) analog and a selective PKA activator.
- GC25420 Fipexide hydrochloride Fipexide (hydrochloride) is a psychoactive drug of the piperazine class.
- GC60886 GSK356278 A selective PDE4 inhbitor
- GC43798 Guanylyl Imidodiphosphate (lithium salt) Guanylyl imidodiphosphate (Gpp(NH)p) lithium, a non-hydrolyzable GTP analogue, increases adenylate cyclase activity.
- GC44022 L-858,051 (hydrochloride) L-858,051 is a water-soluble analog of forskolin, a cell-permeant activator of adenylate cyclase.
- GC49440 ML-9 A PKB/Akt inhibitor
- GC48469 Moexipril-d5 An internal standard for the quantification of moexipril
- GC49186 O-Demethyl Apremilast An active metabolite of apremilast
- GC18951 Obscurolide A1 Obscurolide A1 is a natural butyrolactone isolated from S.
- GC47931 PDE4B Inhibitor A PDE4B inhibitor
- GC41635 Phosphodiesterase 4 Inhibitor Phosphodiesterase 4 (PDE4) inhibitor is an inhibitor of PDE4 with an IC50 value of 0.10 μM for the human recombinant enzyme.
- GC48329 PKA Inhibitor (5-24) (trifluoroacetate salt) A synthetic peptide inhibitor of PKA
- GC44673 PQ-10 PQ-10 is a potent and selective inhibitor of phosphodiesterase type 10 (PDE10; Ki = 4 nM).
- GC18751 Reticulol Reticulol is an isocoumarin derivative produced by certain species of Streptomyces that inhibits cAMP phosphodiesterase (IC50 = 41 uM).
- GC44852 Rp-8-bromo-Cyclic AMPS (sodium salt) Rp-8-bromo-Cyclic AMPS (Rp-8-bromo-cAMPS) is a cell-permeable cAMP analog that combines an exocyclic sulfur substitution in the equatorial position of the cyclophosphate ring with a bromine substitution in the adenine base of cAMP.
- GC10005 SEP-0372814 A PDE10A inhibitor
- GC18532 Skyrin Skyrin is a fungal metabolite characterized by a bisanthraquinone structure.
- GC44920 Sp-8-bromo-Cyclic AMPS (sodium salt) Sp-8-bromo-cyclic AMPS (Sp-8-bromo-cAMPS) is a cell-permeable, cAMP analog that combines an exocyclic sulfur substitution in the axial position of the cyclophosphate ring with a bromine substitution in the adenine base of cAMP.