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홈 >> 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. 상품명 정보
  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-모노숙시닐아데노신-3',5'-사이클릭 모노포스페이트는 아세틸콜린에스테라제에 공유 결합될 수 있는 cAMP 유사체입니다. 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

    세포막 투과성을 가진 cAMP 아날로그로 PKA를 활성화합니다.

     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 cAMP 유사체인 cAMPS-Rp, 트리에틸암모늄 염은 cAMP 의존성 PKA I 및 II(각각 12.5 μM 및 4.5 ⋼M의 Kis) 길항제의 강력하고 경쟁적인 cAMP 유도 활성화입니다. cAMPS-Rp, triethylammonium salt Chemical Structure
  12. GC12706 cAMPS-Sp, triethylammonium salt cAMP 유사체인 cAMPS-Sp, triethylammonium 염은 cAMP 의존성 PKA I 및 II(각각 12.5 μ, M 및 4.5 ⋼, M의 Kis) 길항제의 강력하고 경쟁적인 cAMP 유도 활성화입니다. 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 디부티릴-cAMP, 나트륨염(디부티릴-cAMP 나트륨염)은 안정화된 고리형 AMP(cAMP) 유사체이자 선택적 PKA 활성화제입니다. 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 GSK356278은 인간 PDE4A, PDE4B 및 PDE4D에 대해 각각 8.6, 8.8 및 8.7의 pIC50을 갖는 포스포디에스테라제 4(PDE4)의 강력하고 선택적인 경구 생체이용 및 뇌 침투 억제제입니다. GSK356278 Chemical Structure
  19. GC43798 Guanylyl Imidodiphosphate (lithium salt)

    Guanylyl imidodiphosphate (Gpp(NH)p) 리튬은 가수분해되지 않는 GTP 아날로그로, 아데닐레이트 싸이클라제 활성을 증가시킵니다.

     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-9는 Akt 키나제의 선택적이고 강력한 억제제로 미오신 경쇄 키나제(MLCK) 및 기질 상호작용 분자 1(STIM1) 활성을 억제합니다. ML-9 억제는 각각 4, 32 및 54μM의 Ki 값으로 MLCK, PKA 및 PKC 활성을 억제합니다. ML-9는 autophagosome 형성을 자극하고 분해를 억제하여 autophagy를 유도합니다. 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-10은 각각 4.6nM 및 13mg/kg의 IC50 및 ED50을 갖는 포스포디에스테라제 10A(PDE10A)의 강력한 억제제입니다. 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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