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Home >> Signaling Pathways >> Others >> Adenylate cyclase

Adenylate cyclase

Adenylyl cyclase is an membrane protein that catalyzes the transformation of ATP (adenosine triphosphate) to cAMP (cyclic adenosine monophosphate ).It exhibits cellular regulatory function.

Products for  Adenylate cyclase

  1. Cat.No. Product Name Information
  2. GC11595 1,9-Dideoxyforskolin inactive analog of forskolin, an adenylyl cyclase activator 1,9-Dideoxyforskolin Chemical Structure
  3. GC17544 2',5'-dideoxy Adenosine

    2ʹ,5ʹ-dd-Ado,NSC 95943

     P-site inhibitor of adenylate cyclase 2',5'-dideoxy Adenosine Chemical Structure
  4. GC65139 9-Cyclopentyladenine monomethanesulfonate

    9-CP-Ade mesylate

     9-Cyclopentyladenine monomethylsulfonate (9-CP-Ade mesylate) is a stable non-competitive adenylate cyclase inhibitor with cell permeable properties. 9-Cyclopentyladenine monomethanesulfonate Chemical Structure
  5. GC65376 AC1-IN-1 AC1-IN-1 is a potent and selective Adenylyl cyclase type 1 (AC1) inhibitor with an IC50 of 0.54 ?M. AC1-IN-1 Chemical Structure
  6. GC70966 Adenylyl cyclase type 2 agonist-1 Adenylyl cyclase type 2 agonist-1 (Compound 73) is a potent agonist of adenylyl cyclase type 2 (AC2) with the EC50 of 90 nM. Adenylyl cyclase type 2 agonist-1 Chemical Structure
  7. GC15976 Bithionol

    CP 3438, NSC 9872, NSC 47129

     potent inhibitor of soluble adenylyl cyclase (sAC) Bithionol Chemical Structure
  8. GC18571 CB-7921220 CB-7921220 is an inhibitor of the adenylyl cyclase (AC) isoforms AC1 and AC6. CB-7921220 Chemical Structure
  9. GC11920 Forskolin

    Coleonol, HL 362, L 751362B, NSC 357088, NSC 375489

     Forskolin is a potent adenylyl cyclase activator with IC50 of 41 nM for type I adenylyl cyclase. Forskolin Chemical Structure
  10. GC13248 Guanylyl Imidodiphosphate

    Guanosine 5'-[β,γ-imido]triphosphate trisodium

     Guanylyl Imidodiphosphate (Guanosine 5'-[β,γ-imido]triphosphate) trisodium is a non-hydrolysable GTP analogue, an activator of ADP-ribosylation factor (ARF) and a potent stimulator of adenylate cyclase. Guanylyl Imidodiphosphate Chemical Structure
  11. GC16334 KH 7

    soluble adenylyl cyclase (sAC) inhibitor

     KH 7 Chemical Structure
  12. GC33296 LRE1 LRE1 is a specific and allosteric inhibitor of soluble adenylyl cyclase. LRE1 Chemical Structure
  13. GC64811 Lysipressin acetate

    CYFQNCPKG-NH2, Lypressin, Lys8-vasopressin, Lysine8-vasopressin, Lysine Vasopressin

     Lysipressin acetate is the acetate form of Lysipressin. Lysipressin acetate Chemical Structure
  14. GC12075 MDL 12330A hydrochloride

    RMI 12330A

     adenylate cyclase inhibitor MDL 12330A hydrochloride Chemical Structure
  15. GC14698 N6-methyladenosine (m6A)

    NSC 29409

     N6-methyladenosine (m6A) is the most prevalent internal (non-cap) modification present in the messenger RNA (mRNA) of all higher eukaryotes. N6-methyladenosine (m6A) Chemical Structure
  16. GC36701 NB001 NB001 (HTS 09836) is an adenylcyclase 1 (AC1) inhibitor which has effect on neural and non-neural pain by modulating AC1 activity. NB001 Chemical Structure
  17. GC12640 NKH 477

    Adehl, Colforsin Dapropate, Colforsin Daropate

     adenylyl cyclase activator NKH 477 Chemical Structure
  18. GC17177 NKY 80

    Adenylyl Cyclase Type V Inhibitor

     adenylyl cyclase (AC) inhibitor NKY 80 Chemical Structure
  19. GC61281 SKF-83566 SKF-83566 is a potent,?blood-brain permeable and orally active D1-like dopamine receptor (D1DR)?antagonist and a weaker competitive antagonist at the vascular 5-HT2?receptor (Ki=11 nM). SKF-83566 Chemical Structure
  20. GC31194 Small Cardioactive Peptide B SCPB Small Cardioactive Peptide B SCPB, a neurally active peptide, stimulates adenylate cyclase activity in particulate fractions of both heart and gill tissues with EC50s of 0.1 and 1.0 μM, respectively. Small Cardioactive Peptide B SCPB Chemical Structure
  21. GC13867 SQ 22536

    NSC 53339

    adenylate cyclase inhibitor

     SQ 22536 Chemical Structure
  22. GC18584 ST034307 ST034307 is an inhibitor of adenylyl cyclase 1 (AC1), a membrane-bound AC, with an IC50 value of 2.3 uM for A23187-stimulated cAMP accumulation in HEK293 cells transfected with AC1. ST034307 Chemical Structure
  23. GC63213 TDI-10229 TDI-10229 is a potent and orally bioavailable inhibitor of soluble adenylyl cyclase (sAC, ADCY10). TDI-10229 Chemical Structure
  24. GC70001 TDI-11861

    TDI-11861 is a second-generation inhibitor of soluble adenylyl cyclase (sAC) with slow dissociation rate. TDI-11861 inhibits sAC with an IC50 of 5.5 nM.

     TDI-11861 Chemical Structure
  25. GC37797 TIP 39, Tuberoinfundibular Neuropeptide TIP 39, Tuberoinfundibular Neuropeptide is a neuropeptide and parathyroid hormone 2 receptor (PTH2R) agonist. TIP 39, Tuberoinfundibular Neuropeptide Chemical Structure
  26. GC72398 Zelminemab Zelminemab (AMG-301) is a humanized monoclonal antibody that inhibits PACAP type I (PAC1) receptor. Zelminemab Chemical Structure
  27. GC72201 [Tyr22] Calcitonin Gene Related Peptide, (22-37), rat [Tyr22] Calcitonin Gene Related Peptide, (22-37), rat is a fragments 22-37 of rat calcitonin gene related peptide (CGRP), targeting CGRP receptor and adenylate cyclase. [Tyr22] Calcitonin Gene Related Peptide, (22-37), rat Chemical Structure
  28. GC14374 α-MSH

    α-Melanocyte-Stimulating Hormone, a-MSH

     Alpha-melanocyte-stimulating hormone (α-MSH) is a neuropeptide with immunomodulatory properties that is produced by post-translational processing of proproiomelanocortin (POMC). α-MSH Chemical Structure

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