Shopping Cart
  • Remove All
  • TargetMol
    Your shopping cart is currently empty
Filter
Applied FilterClear all
TargetMol | Tags By Target
  • cAMP
    (42)
  • PDE
    (24)
  • PKA
    (17)
  • Adrenergic Receptor
    (11)
  • Endogenous Metabolite
    (11)
  • ADC Cytotoxin
    (10)
  • Apoptosis
    (10)
  • Prostaglandin Receptor
    (9)
  • Autophagy
    (7)
  • Others
    (176)
Filter
Search Result
Results for "

cAMP

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    502
    TargetMol | Inhibitors_Agonists
  • Compound Libraries
    1
    TargetMol | Compound_Libraries
  • Peptide Products
    79
    TargetMol | Peptide_Products
  • Dye Reagents
    4
    TargetMol | Dye_Reagents
  • Natural Products
    84
    TargetMol | Natural_Products
  • Recombinant Protein
    44
    TargetMol | Recombinant_Protein
  • Isotope Products
    7
    TargetMol | Isotope_Products
  • Antibody Products
    10
    TargetMol | Antibody_Products
  • Disease Modeling
    1
    TargetMol | Disease_Modeling_Products
  • Cell Research
    2
    TargetMol | Inhibitors_Agonists
Rp-cAMPS sodium
T36679142439-94-9
Rp-cAMPS sodium is a phosphorothioate analog of cAMP, a protein kinase A inhibitor and a membrane-permeable cAMP antagonist that inhibits cAMP-dependent protein kinases by blocking cAMP-induced conformational transitions, and can be used in the study of cardiovascular diseases.
  • Inquiry Price
6-8 weeks
Size
QTY
MRE3008F20
T16132252979-43-4In house
MRE3008F20 is a species-selective and potent adenosine A3 receptor (AA3R) antagonist that inhibits Cl-IB-MECA-induced cAMP production and can be used in glaucoma and asthma studies.13483-88-88-9
  • Inquiry Price
6-8 weeks
Size
QTY
UNC0006
UNC-0006, UNC 0006
T290611354030-14-0In house
UNC0006 is a beta-inhibitory protein biased D(2)R ligand, and is also an antagonist of G(i)-regulated cAMP production and a partial agonist of D(2)R beta-arrestin-2 interaction. It has antipsychotic activity and is used in the study of neurological disorders.
  • Inquiry Price
6-8 weeks
Size
QTY
CB1R Allosteric modulator 3
T615622633686-36-7
CB1R Allosteric modulator 3 is a potent CB1R modulator that inhibits cAMP and β-Arrestin and can be used for the study of obesity and nicotine addiction.
  • Inquiry Price
6-8 weeks
Size
QTY
Evocarpine
TN112115266-38-3
Evocarpine shows antimycobacterial, and vasorelaxant effects, it can inhibit Ca2+ influx through voltage-dependent calcium channels.
  • Inquiry Price
Size
QTY
Eriocalyxin B
TN162084745-95-9
Eriocalyxin B induces apoptosis and cell cycle arrest in pancreatic adenocarcinoma cells through caspase- and p53-dependent pathways, should be considered a candidate for pancreatic cancer treatment; it is a specific inhibitor of STAT3, it directly target
  • Inquiry Price
Size
QTY
TargetMol | Inhibitor Sale
Bucladesine sodium
Sodium dibutyryl cAMP, Dibutyryl-cAMP sodium salt, Dibutyryl-cAMP, DC2797, dbcAMP, Bucladesine sodium salt, Bucladesine
T141816980-89-5
Bucladesine sodium (DC2797) is a cAMP analog with cell-permeable properties. Bucladesine sodium is also a cAMP-dependent protein kinase (PKA) activator and a phosphodiester (PDE) inhibitor. Bucladesine sodium has anti-inflammatory activity.
  • Inquiry Price
Size
QTY
TargetMol | Inhibitor Hot
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.
  • Inquiry Price
Size
QTY
TargetMol | Inhibitor Hot
LGD-6972
T118451207989-09-0In house
LGD-6972 is an antagonist of glucagon receptor.
  • Inquiry Price
8-10 weeks
Size
QTY
bc 11-38
T21865686770-80-9In house
BC 11-38 is a potent, selective PDE biodepressant which is mainly effective against PDE11 (IC50 : 0.28 μM).
  • Inquiry Price
Size
QTY
TargetMol | Inhibitor Sale
Cyclic AMP
Cyclic 3',5'-monophosphate adenosine, cAMP, Adenosine Cyclophosphate, Adenosine 3',5'-cyclophosphate, 3',5'-AMP
TCO274560-92-4
Cyclic AMP (cAMP) (Adenosine 3',5'-cyclophosphate) combined with vitamin C treatment of children with viral myocarditis has exact curative effect, and it can improve cardiac function of patients and improve immune function.
  • Inquiry Price
Size
QTY
cj-42794
CJ-042794
T14975847728-01-2
CJ-42794 (CJ-042794) is a selective antagonist of the prostaglandin E receptor subtype 4 (EP4), inhibiting [3H]-PGE2 binding to the human EP4 receptor with a mean pKi of 8.5. It exhibits a binding affinity that is at least 200-fold more selective for the human EP4 receptor than for other human EP receptor subtypes (EP1, EP2, and EP3) (IC50: 8.5 (pKi)).
  • Inquiry Price
6-8 weeks
Size
QTY
Ro 20-1724
Ro20-1724, Ro-20-1724, 4-(3-Butoxy-4-methoxybenzyl)-2-imidazolidinone
T1970629925-17-5
Ro 20-1724 (4-(3-Butoxy-4-methoxybenzyl)-2-imidazolidinone) is a widely used inhibitor of cyclic nucleotide phosphodiesterase with IC50 of 2.0 μM and Ki of 3.1 μM.
  • Inquiry Price
Size
QTY
Setipiprant
KYTH-105, ACT-129968
T3520866460-33-5
Setipiprant (ACT-129968) is an orally available, selective CRTH2 antagonist (IC50: 6.0 nM). CRTH2, a G protein-coupled receptor for prostaglandin (PGD2), mediates key inflammatory responses related to allergy and asthma. PGD2, produced by mast cells, binds to CRTH2 on blood-borne cells, inducing chemotaxis of Th2 cells, basophils, and eosinophils, and stimulating cytokine release.
  • Inquiry Price
Size
QTY
Actein
T719018642-44-9
Actein has a stimulatory effect on osteoblastic bone formation or has potential activity against osteoporosis, it also can prevent oxidative damage to osteoblasts in osteoporotic patients. Actein's ability to pathways involved in lipid disorders and carci
  • Inquiry Price
Size
QTY
Trans-caffeic acid
3,4-Dihydroxybenzeneacrylic acid
TMA0003501-16-6
Trans-caffeic acid (3,4-Dihydroxybenzeneacrylic acid) can be used as a highly sensitive fluorescent probe for the detection of laccase in food and can also stimulate the growth of germ tissue.
  • Inquiry Price
Size
QTY
β-Amyrin
beta-Amyrin
TN1027559-70-6
β-Amyrin (beta-Amyrin) has antiviral, hepatoprotective, antinociceptive, anti-inflammatory
  • Inquiry Price
Size
QTY
TargetMol | Inhibitor Sale
8-Bromo-cAMP sodium salt
8-Bromo-cAMP(sodium salt), 8-Br-Camp sodium salt
T674776939-46-3
8-Bromo-cAMP sodium salt (8-Br-Camp sodium salt) is a long-acting derivative of cyclic AMP. It is an activator of cyclic AMP-dependent protein kinase(PKA), but resistant to degradation by cyclic AMP phosphodiesterase.
  • Inquiry Price
Size
QTY
8-CPT-cAMP
8-(4-Chlorophenylthio)-cAMP
T20224041941-66-6
8-CPT-cAMP is a PDE Va inhibitor.
  • Inquiry Price
Size
QTY
8-CPT-2Me-cAMP, sodium salt
T22014634207-53-7
8-CPT-2Me-cAMP sodium is a sodium salt compound that selectively activates exchange proteins activated by cAMP (Epac), which are cAMP-sensitive guanine nucleotide exchange factors (GEFs) responsible for activating small GTPases Rap1 and Rap2. It specifically activates Epac1 with an EC50 value of 2.2 μM, while showing no activation of PKA with an EC50 value greater than 10 μM [1]. Additionally, 8-CPT-2Me-cAMP sodium stimulates the Epac-mediated release of calcium ions (Ca2+) in vitro in pancreatic β-cells [2].
  • Inquiry Price
6-8 weeks
Size
QTY
6-Bnz-cAMP sodium salt
T225291135306-29-4
6-Bnz-cAMP is a PKA-selective activator. It regulates the PKA dependent signaling pathways. The proliferative signaling pathway which activated by the 6-Bnz-cAMP involves activation of the epidermal growth factor receptor and ERK1/2. Extending the duratio
  • Inquiry Price
8-10 weeks
Size
QTY
8-pCPT-2-O-Me-cAMP-AM
T225361152197-23-3
Epac activator
  • Inquiry Price
Size
QTY
2'-O-Succinyl-cAMP
T3542136940-87-1
2'-O-Monosuccinyladenosine-3',5'-cyclic monophosphate is an immunogenic derivative of cAMP that has been used to generate anti-cAMP antisera and antibodies.1,2
  • Inquiry Price
Size
QTY
8-HA-cAMP
8-Hexylamino-cAMP
T8844559212-44-1
8-HA-cAMP is a membrane-permeable analog of cAMP and an activator of cAMP-dependent protein kinase and PKAI. It exhibits metabolic stability against mammalian cyclic nucleotide phosphodiesterases.
  • Inquiry Price
10-14 weeks
Size
QTY