Home >> Signaling Pathways >> MAPK Signaling >> cAMP

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

  1. Cat.No. Product Name Information
  2. GC48920 β-Carboline-1-carboxylic Acid An alkaloid with diverse biological activities β-Carboline-1-carboxylic Acid  Chemical Structure
  3. 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. 2'-O-Monosuccinyladenosine-3',5'-cyclic monophosphate  Chemical Structure
  4. GC48381 5'-pApA (sodium salt) A linearized form of cyclic di-AMP 5'-pApA (sodium salt)  Chemical Structure
  5. GC41423 5-trans Prostaglandin E2 5-trans PGE2 occurs naturally in some gorgonian corals and is a common impurity in commercial lots of PGE1. 5-trans Prostaglandin E2  Chemical Structure
  6. GC12834 6-Bnz-cAMP sodium salt cAMP analog,PKA activator 6-Bnz-cAMP sodium salt  Chemical Structure
  7. GC42616 7-oxo Staurosporine

    7-oxo Staurosporine is an antibiotic originally isolated from S.

    7-oxo Staurosporine  Chemical Structure
  8. GC16929 8-Bromo-cAMP, sodium salt Cell-permeable cAMP analog that activates PKA 8-Bromo-cAMP, sodium salt  Chemical Structure
  9. 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. 8-bromo-Cyclic AMP  Chemical Structure
  10. GC49285 Adenosine 5’-methylenediphosphate (hydrate) An inhibitor of ecto-5’-nucleotidase Adenosine 5’-methylenediphosphate (hydrate)  Chemical Structure
  11. 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. cAMPS-Rp, triethylammonium salt  Chemical Structure
  12. 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. cAMPS-Sp, triethylammonium salt  Chemical Structure
  13. GC47088 Cilostazol-d4 An internal standard for the quantification of cilostazol Cilostazol-d4  Chemical Structure
  14. GC43339 Cyclic di-AMP (sodium salt) Cyclic di-AMP (c-di-AMP) is a second messenger produced by bacteria but not by mammals. Cyclic di-AMP (sodium salt)  Chemical Structure
  15. GC43341 Cyclic GMP

    Guanosine 3',5'-cyclic monophosphate (cyclic GMP or cGMP) is a second messenger that is biosynthesized from GTP by guanylate cyclases.

    Cyclic GMP  Chemical Structure
  16. 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. Dibutyryl-cAMP, sodium salt  Chemical Structure
  17. GC25420 Fipexide hydrochloride Fipexide (hydrochloride) is a psychoactive drug of the piperazine class. Fipexide hydrochloride  Chemical Structure
  18. GC60886 GSK356278 A selective PDE4 inhbitor GSK356278  Chemical Structure
  19. GC43798 Guanylyl Imidodiphosphate (lithium salt) Guanylyl imidodiphosphate (Gpp(NH)p) lithium, a non-hydrolyzable GTP analogue, increases adenylate cyclase activity. Guanylyl Imidodiphosphate (lithium salt)  Chemical Structure
  20. GC44022 L-858,051 (hydrochloride) L-858,051 is a water-soluble analog of forskolin, a cell-permeant activator of adenylate cyclase. L-858,051 (hydrochloride)  Chemical Structure
  21. GC49440 ML-9 A PKB/Akt inhibitor ML-9  Chemical Structure
  22. GC48469 Moexipril-d5 An internal standard for the quantification of moexipril Moexipril-d5  Chemical Structure
  23. GC49186 O-Demethyl Apremilast An active metabolite of apremilast O-Demethyl Apremilast  Chemical Structure
  24. GC18951 Obscurolide A1 Obscurolide A1 is a natural butyrolactone isolated from S. Obscurolide A1  Chemical Structure
  25. GC47931 PDE4B Inhibitor A PDE4B inhibitor PDE4B Inhibitor  Chemical Structure
  26. 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. Phosphodiesterase 4 Inhibitor  Chemical Structure
  27. GC48329 PKA Inhibitor (5-24) (trifluoroacetate salt) A synthetic peptide inhibitor of PKA PKA Inhibitor (5-24) (trifluoroacetate salt)  Chemical Structure
  28. GC44673 PQ-10 PQ-10 is a potent and selective inhibitor of phosphodiesterase type 10 (PDE10; Ki = 4 nM). PQ-10  Chemical Structure
  29. GC18751 Reticulol Reticulol is an isocoumarin derivative produced by certain species of Streptomyces that inhibits cAMP phosphodiesterase (IC50 = 41 uM). Reticulol  Chemical Structure
  30. 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. Rp-8-bromo-Cyclic AMPS (sodium salt)  Chemical Structure
  31. GC10005 SEP-0372814 A PDE10A inhibitor SEP-0372814  Chemical Structure
  32. GC18532 Skyrin Skyrin is a fungal metabolite characterized by a bisanthraquinone structure. Skyrin  Chemical Structure
  33. 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. Sp-8-bromo-Cyclic AMPS (sodium salt)  Chemical Structure

32 Item(s)

per page

Set Descending Direction