Shopping Cart
Remove All
  • TargetMol
    Your shopping cart is currently empty

Adenylate cyclase

Adenylate cyclase (AC) is a membrane-bound enzyme whose core function is to catalyze the conversion of adenosine triphosphate (ATP) into the second messenger cyclic adenosine monophosphate (cAMP), thereby translating extracellular chemical signals into intracellular signaling cascades. Adenylate cyclase serves not only as a key downstream effector of G protein-coupled receptors (GPCRs), but its transmembrane domain itself can also function as a direct receptor for lipid signals. This dual regulatory mechanism has opened up entirely new directions for drug target research in cardiovascular, neurological, and metabolic diseases.

Forskolin
FSK, Colforsin, Coleonol
T293966575-29-9
Forskolin (Coleonol) is a natural product, an adenylate cyclase activator (EC50=0.5 μM). Forskolin increases cAMP levels, activates PXR and FXR, and induces autophagy. Forskolin produces positive inotropic effects in the heart, and has platelet anticoagulant and antihypertensive effects.
  • $36
In Stock
Size
QTY
TargetMol | Inhibitor Hot
TargetMol | Citations Cited
α-MSH
α-Melanocyte-Stimulating Hormone (MSH), amide, MSH, amide, CZEN-002
T7813581-05-5
α-MSH (MSH, amide) is amide stimulates melanocortin 1 receptor that results in the activation of adenylyl cyclase.
  • $53
In Stock
Size
QTY
TargetMol | Citations Cited
AC1-IN-1
T600032762422-55-7
AC1-IN-1 is a selective inhibitor of adenylyl cyclase type 1 (AC1, IC50 = 0.54 µM).
  • $83
In Stock
Size
QTY
9-Cyclopentyladenine
NSC-19486, NSC19486, NSC 19486, 9-CP-Ade, 9CPAde, 9 CP Ade
T29652715-91-3In house
9-Cyclopentyladenine (NSC-19486) is an adenylate cyclase inhibitor that blocks cellular morphological differentiation and phosphorylation of specific signaling molecules.
  • $195
In Stock
Size
QTY
Zelminemab
AMG-301, AMG301
T769492225850-33-7
Zelminemab (AMG-301) is a humanized monoclonal antibody targeting the pituitary adenylate cyclase-activating polypeptide type I receptor (ADCYAP1R1) for use in neurological disorders.
  • $197
In Stock
Size
QTY
SQ22536
SQ 22536, 9-(tetrahydrofuran-2-yl)-9h-purin-6-amine
T217217318-31-9
SQ22536 (9-(tetrahydrofuran-2-yl)-9h-purin-6-amine) , the adenosine analogue 9-(Tetrahydro-2-furyl)adenine, inhibited adenylate cyclase activity of crude membrane preparations from catfish (Ictalurus melas) and rat isolated hepatocytes in a non-competitive manner.
  • $30
In Stock
Size
QTY
TargetMol | Citations Cited
NB001
HTS 09836
T16275686301-48-4In house
NB001 (HTS 09836) is an adenyl cyclase 1 inhibitor that affects both neural and non-neural pain.
  • $72
In Stock
Size
QTY
ST034307
T16938133406-29-8
ST034307 is an effective and selective inhibitor of adenylyl cyclase 1 (IC50: 2.3 μM).
  • $32
In Stock
Size
QTY
Fipexide
T032234161-24-5
Fipexide (Attentil, Vigilor), a psychoactive drug of the piperazine chemical class, was developed in Italy in 1983. It was served as a nootropic drug in France and Italy, mainly for the therapy of senile dementia, but is no longer in common use because of the occurrence of rare drug side-effects including hepatitis and fever.
  • $31
In Stock
Size
QTY
KH7
T15658330676-02-3
KH7 is a soluble inhibitor of adenylyl cyclase (sAC)-specific. It has IC50s of 3-10 μM toward both recombinant purified human sACt protein and heterologously expressed sACt in cellular assays. KH7 is also a cAMP inhibitor.
  • $37
In Stock
Size
QTY
TargetMol | Citations Cited
2',5'-Dideoxyadenosine
T100666698-26-6
2',5'-Dideoxyadenosine is a potent and non-competitive adenylyl cyclase inhibitor, binding to the P-site with an IC50 of 3 μM.
  • $33
In Stock
Size
QTY
NKY80
Adenylyl cyclase type V Inhibitor
T16333299442-43-6
NKY80 regulates the adenylyl cyclase catalytic activity in heart and lung tissues. NKY80 is a non-competitive inhibitor of adenylyl cyclase type V isoform (IC50s: 8.3 µM, 132 µM, and 1.7 mM for type V, III and II, respectively).
  • $39
In Stock
Size
QTY
LRE1
T157871252362-53-0
LRE1 is a specific and allosteric inhibitor of soluble adenylyl cyclase (sAC).
  • $35
In Stock
Size
QTY
Clorprenaline
T602613811-25-4
Clorprenaline is a β-adrenergic receptor agonist that activates adenylate cyclase and PKA and upregulates cAMP, leading to relaxation of bronchial smooth muscle cells, dilation of the airway, and improvement of airflow. Clorprenaline inhibits the release of mediators, such as histamine and leukotrienes, from mast cells, further promoting its anti-inflammatory properties.
  • $40
In Stock
Size
QTY
Wnt pathway inhibitor 3
T77502663213-98-7
Wnt pathway inhibitor 3 is a potent AC1 inhibitor (IC50: 45 nM) with antiproliferative activity, suitable for studies to ameliorate osteoarthritis in a mouse model of experimental osteoarthritis.
  • $33
In Stock
Size
QTY
9-CP-Ade Mesylate
9-Cyclopentyladenine monomethanesulfonate, 9CPAde Mesylate, 9 CP Ade Mesylate
T23588189639-09-6In house
9-CP-Ade Mesylate (9 CP Ade Mesylate) is a cell-permeable, stable and non-competitive inhibitor of adenylate cyclase.
  • $61
In Stock
Size
QTY
CB-7921220
6-[2-(4-Aminophenyl)vinyl]-2-pyridinecarboxylic acid, 6-[(E)-2-(4-aminophenyl)ethenyl]pyridine-2-carboxylic acid, 6-(4-Aminostyryl)picolinic acid
T14880115453-99-1
CB-7921220 (6-[2-(4-Aminophenyl)vinyl]-2-pyridinecarboxylic acid) is an inhibitor of adenylate cyclase.
  • $39
In Stock
Size
QTY
NKH477
NKH 477, Colforsin dapropate hydrochloride
T16332138605-00-2
NKH477 (Colforsin dapropate hydrochloride) is a derivative of forskolin with antidepressant activity. It inhibits ACh-induced Ca2+ mobilization by acting on ionomycin-sensitive storage sites. NKH477 is an adenylyl cyclase activator with bronchodilatory effects, inhibiting the production of CTL, T-cell proliferation in mixed lymphocyte reactions (MLR), as well as IL-2 production and mitogen responses.
  • $149
In Stock
Size
QTY
TargetMol | Citations Cited
2-Chloro-ADP
2-Chloroadenosine 5′-diphosphate
T20365216506-88-0
2-Chloro-ADP (2-Chloroadenosine 5′-diphosphate) is a derivative of Adenosine 5'-diphosphate (ADP) that induces platelet aggregation and inhibits stimulated adenylate cyclase. Additionally, 2-Chloro-ADP can inhibit the nucleotide-binding domain (NBD) of Mortalin with a Ki value of 45.05 μM.
  • Inquiry Price
10-14 weeks
Size
QTY