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Startseite >> 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.

Produkte für  cAMP

  1. Bestell-Nr. Artikelname Informationen
  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'-cyclisches Monophosphat ist ein cAMP-Analogon, das kovalent an Acetylcholinesterase gekoppelt werden kann. 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

    Zellpermeables cAMP-Analogon, das PKA aktiviert.

     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, Triethylammoniumsalz, ein cAMP-Analogon, ist ein potenter, kompetitiver cAMP-induzierter Aktivierung von cAMP-abhÄngigen PKA I- und II-Antagonisten (Kis von 12,5 μM und 4,5 μM). cAMPS-Rp, triethylammonium salt Chemical Structure
  12. GC12706 cAMPS-Sp, triethylammonium salt cAMPS-Sp, Triethylammoniumsalz, ein cAMP-Analogon, ist ein potenter, kompetitiver cAMP-induzierter Antagonist der cAMP-abhÄngigen PKA I und II (Kis von 12,5 μM und 4,5 μM). 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, Natriumsalz (Dibutyryl-cAMP-Natriumsalz) ist ein stabilisiertes cyclisches AMP (cAMP)-Analogon und ein selektiver PKA-Aktivator. 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 ist ein potenter, selektiver, oral bioverfÜgbarer und ins Gehirn eindringender Inhibitor der Phosphodiesterase 4 (PDE4) mit pIC50-Werten von 8,6, 8,8 und 8,7 fÜr humane PDE4A, PDE4B bzw. PDE4D. GSK356278 Chemical Structure
  19. GC43798 Guanylyl Imidodiphosphate (lithium salt)

    Guanylyl-Imidodiphosphat (Gpp(NH)p) Lithium, ein nicht hydrolysierbares GTP-Analogon, erhöht die Adenylatzyklase-Aktivität.

     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 ist ein selektiver und potenter Inhibitor der Akt-Kinase, hemmt die AktivitÄt der Myosin-Leichtketten-Kinase (MLCK) und des stromalen InteraktionsmolekÜls 1 (STIM1). ML-9 hemmt die MLCK-, PKA- und PKC-AktivitÄt mit Ki-Werten von 4, 32 bzw. 54μM. ML-9 induziert Autophagie, indem es die Bildung von Autophagosomen stimuliert und deren Abbau hemmt. 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 ist ein potenter Inhibitor der Phosphodiesterase 10A (PDE10A) mit IC50 und ED50 von 4,6 nM bzw. 13 mg/kg. 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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