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Inicio >> 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. Nombre del producto Información
  2. GC48920 β-Carboline-1-carboxylic Acid

    1-Formic Acid-β-carboline

     An alkaloid with diverse biological activities β-Carboline-1-carboxylic Acid Chemical Structure
  3. GC46554 2'-O-Monosuccinyladenosine-3',5'-cyclic monophosphate

    2’-O-Succinyl-cAMP, 2’-O-Succinyl-3’,5’-cyclic AMP

     2'-O-Monosuccinyladenosine-3',5'-el monofosfato cÍclico es un anÁlogo de AMPc que puede acoplarse covalentemente a la acetilcolinesterasa. 2'-O-Monosuccinyladenosine-3',5'-cyclic monophosphate Chemical Structure
  4. GC48381 5'-pApA (sodium salt)

    c-di-AMP Control, Cyclic di-AMP Negative Control

     A linearized form of cyclic di-AMP 5'-pApA (sodium salt) Chemical Structure
  5. GC41423 5-trans Prostaglandin E2

    transDinoprostone, 5,6trans PGE2

     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

    6-Bnz-cAMP

     cAMP analog,PKA activator 6-Bnz-cAMP sodium salt Chemical Structure
  7. GC42616 7-oxo Staurosporine

    BMY 41950, RK-1409

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

     7-oxo Staurosporine Chemical Structure
  8. GC16929 8-Bromo-cAMP, sodium salt

    8-Br-cAMP, 8-Bromoadenosine 3',5'-cyclic monophosphate, 8-bromo-cAMP

    Análogo de cAMP permeable a la célula que activa PKA.

     8-Bromo-cAMP, sodium salt Chemical Structure
  9. GC42622 8-bromo-Cyclic AMP

    8-Bromoadenosine 3',5'-cyclic monophosphate, 8-Br-cAMP, 8-bromo-cAMP, NSC 171719

     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. GC42630 8-pCPT-2'-O-Me-Cyclic AMP (sodium salt)

    Exchange proteins activated by cAMP (Epacs) are guanine nucleotide exchange factors (GEFs) for the small GTPases Rap1 and Rap2.

     8-pCPT-2'-O-Me-Cyclic AMP (sodium salt) Chemical Structure
  11. GC90794 Adenosine 5'-methylenediphosphate (sodium salt)

    Un inhibidor de la ecto-5'-nucleotidasa.

     Adenosine 5'-methylenediphosphate (sodium salt) Chemical Structure
  12. GC49285 Adenosine 5’-methylenediphosphate (hydrate)

    Adenosine 5'-(α,β-methylene)diphosphate, AMP-CP, APCP, 5'-APCP

     An inhibitor of ecto-5’-nucleotidase Adenosine 5’-methylenediphosphate (hydrate) Chemical Structure
  13. GC48870 Anagrelide-13C3

    BL 4162A-13C3, BMY 26538-01-13C3

     Anagrelide-13C3 Chemical Structure
  14. GC10941 cAMPS-Rp, triethylammonium salt

    Rp-cAMPS

     cAMPS-Rp, sal de trietilamonio, un anÁlogo de cAMP, es un antagonista potente y competitivo de la activaciÓn inducida por cAMP de PKA I y II dependiente de cAMP (Kis de 12,5 μM y 4,5 μM, respectivamente). cAMPS-Rp, triethylammonium salt Chemical Structure
  15. GC12706 cAMPS-Sp, triethylammonium salt cAMPS-Sp, sal de trietilamonio, un anÁlogo de cAMP, es un potente antagonista competitivo inducido por la activaciÓn de cAMP de cAMP dependiente de PKA I y II (Kis de 12,5 μM y 4,5 μM, respectivamente). cAMPS-Sp, triethylammonium salt Chemical Structure
  16. GC47088 Cilostazol-d4 An internal standard for the quantification of cilostazol Cilostazol-d4 Chemical Structure
  17. GC43341 Cyclic GMP

    cGMP, Cyclic guanosine monophosphate, Guanosine 3'5'-cyclic monophosphate, Monosodium-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
  18. GC12824 Dibutyryl-cAMP, sodium salt

    DC 2797

     La sal sÓdica de dibutiril-cAMP (sal sÓdica de dibutiril-cAMP) es un anÁlogo del AMP cÍclico estabilizado (cAMP) y un activador selectivo de la PKA. Dibutyryl-cAMP, sodium salt Chemical Structure
  19. GC47237 Dipyridamole-d16 A neuropeptide with diverse biological activities Dipyridamole-d16 Chemical Structure
  20. GC25420 Fipexide hydrochloride Fipexide (hydrochloride) is a psychoactive drug of the piperazine class. Fipexide hydrochloride Chemical Structure
  21. GC60886 GSK356278 GSK356278 es un inhibidor de la fosfodiesterasa 4 (PDE4) potente, selectivo, biodisponible por vÍa oral y que penetra en el cerebro, con pIC50 de 8,6, 8,8 y 8,7 para las PDE4A, PDE4B y PDE4D humanas, respectivamente. GSK356278 Chemical Structure
  22. GC43798 Guanylyl Imidodiphosphate (lithium salt)

    Gpp(NH)p lithium

    El guanil imidodifosfato (Gpp(NH)p) de litio, un análogo no hidrolizable del GTP, aumenta la actividad de la adenilato ciclasa.

     Guanylyl Imidodiphosphate (lithium salt) Chemical Structure
  23. 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
  24. GC40231 Milrinone-d3 Milrinone-d3 is intended for use as an internal standard for the quantification of milrinone by GC- or LC-MS. Milrinone-d3 Chemical Structure
  25. GC48469 Moexipril-d5 An internal standard for the quantification of moexipril Moexipril-d5 Chemical Structure
  26. GC49186 O-Demethyl Apremilast

    4'-hydroxy APR

     An active metabolite of apremilast O-Demethyl Apremilast Chemical Structure
  27. GC18951 Obscurolide A1 Obscurolide A1 is a natural butyrolactone isolated from S. Obscurolide A1 Chemical Structure
  28. GC47931 PDE4B Inhibitor

    KVA-D-88

     A PDE4B inhibitor PDE4B Inhibitor Chemical Structure
  29. GC41635 Phosphodiesterase 4 Inhibitor

    PDE4 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
  30. GC48329 PKA Inhibitor (5-24) (trifluoroacetate salt)

    PKI (524), Protein Kinase A Inhibitor (524)

     A synthetic peptide inhibitor of PKA PKA Inhibitor (5-24) (trifluoroacetate salt) Chemical Structure
  31. GC44673 PQ-10 PQ-10 es un potente inhibidor de la fosfodiesterasa 10A (PDE10A) con IC50 y ED50 de 4,6 nM y 13 mg/kg, respectivamente. PQ-10 Chemical Structure
  32. GC18751 Reticulol

    6,8-dihydroxy-7-methoxy-3-methyl Isocoumarin, NSC 294978

     Reticulol is an isocoumarin derivative produced by certain species of Streptomyces that inhibits cAMP phosphodiesterase (IC50 = 41 uM). Reticulol Chemical Structure
  33. GC44852 Rp-8-bromo-Cyclic AMPS (sodium salt)

    8-Bromoadenosine 3',5'-cyclic monophosphorothioate, Rp-isomer, Rp-8-BrcAMPS, Rp-8-bromocAMPS

     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
  34. GC10005 SEP-0372814 A PDE10A inhibitor SEP-0372814 Chemical Structure
  35. GC18532 Skyrin

    Endothianin, Rhodophyscin

     Skyrin is a fungal metabolite characterized by a bisanthraquinone structure. Skyrin Chemical Structure
  36. GC44920 Sp-8-bromo-Cyclic AMPS (sodium salt)

    8Bromoadenosine 3',5'cyclic Monophosphothioate SPIsomer, Sp8bromocAMPS

     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
  37. GC90924 TNP-GTP (sodium salt)

    Un derivado fluorescente de GTP

     TNP-GTP (sodium salt) Chemical Structure

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