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Accueil >> 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. Nom du produit Informations
  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'-le monophosphate cyclique est un analogue de l'AMPc qui peut être couplé de manière covalente À l'acétylcholinestérase. 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

    Analogue de cAMP perméable à la cellule qui active 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 L'AMPc-Rp, sel de triéthylammonium, un analogue de l'AMPc, est une activation puissante et compétitive induite par l'AMPc des PKA I et II dépendantes de l'AMPc (Kis de 12,5 μ ; M et 4,5 μ ; M, respectivement). cAMPS-Rp, triethylammonium salt Chemical Structure
  12. GC12706 cAMPS-Sp, triethylammonium salt L'AMPc-Sp, sel de triéthylammonium, un analogue de l'AMPc, est une activation puissante et compétitive induite par l'AMPc des PKA I et II dépendantes de l'AMPc (Kis de 12,5 μ ; M et 4,5 μ ; M, respectivement). 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-AMPc, sel de sel de sodium (sel de sodium de Dibutyryl-AMPc) est un analogue de l'AMP cyclique stabilisé (AMPc) et un activateur sélectif de la PKA. 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 GSK356278 est un inhibiteur puissant, sélectif, biodisponible par voie orale et pénétrant dans le cerveau de la phosphodiestérase 4 (PDE4), avec des pIC50 de 8,6, 8,8 et 8,7 pour les PDE4A, PDE4B et PDE4D humaines, respectivement. GSK356278 Chemical Structure
  19. GC43798 Guanylyl Imidodiphosphate (lithium salt)

    Le guanylyl imidodiphosphate (Gpp(NH)p) lithium, un analogue non hydrolysable du GTP, augmente l'activité de l'adénylate cyclase.

     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 ML-9 est un inhibiteur sélectif et puissant de la kinase Akt, inhibe l'activité de la kinase de la chaÎne légère de la myosine (MLCK) et de la molécule d'interaction stromale 1 (STIM1). ML-9 inhibe l'activité MLCK, PKA et PKC avec des valeurs Ki de 4, 32 et 54μM, respectivement. ML-9 induit l'autophagie en stimulant la formation d'autophagosomes et en inhibant leur dégradation. 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 Le PQ-10 est un puissant inhibiteur de la phosphodiestérase 10A (PDE10A) avec une IC50 et une DE50 de 4,6 nM et 13 mg/kg, respectivement. 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

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