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cAMP

cAMP

货号 产品名 CAS号 信息
CSN20479 ST034307 133406-29-8 ST034307 is an adenylyl cyclase 1 (AC1) inhibitor (IC50 = 2.3 μM), which exhibits some selectivity for AC1 over other AC isoforms.
CSN11972 SQ22536 17318-31-9 SQ22536 is an inhibitor of adenylyl cyclase with an IC50 of 1.4 μM. It can inhibit PGE1-stimulated increases in cAMP levels in intact human platelets.
CSN17016 (E)-5-(4-Hydroxystyryl)benzene-1,3-diol 501-36-0 Resveratrol is one of the numerous polyphenolic compounds found in several vegetal sources, has a wide spectrum of targets with IC50 of 0.8, 1, 3.3 and 5 μM for Adenylyl cyclase, IKKβ, DNA polymerase α and δ, respectively.
CSN21676 PACAP (6-38), human, ovine, rat 143748-18-9 PACAP 6-38 blocks the CARTp-induced phosphorylation of ERK in differentiated cells.
CSN21673 PACAP (1-38), human, ovine, rat 137061-48-4 PACAP 1-38 is a potent PACAP receptor agonist with IC50s of 4 nM, 2 nM, and 1 nM for PACAP type I receptor, PACAP type II receptor VIP1, and PACAP type II receptor VIP2 respectively.
CSN26406 NKH477 138605-00-2 NKH477 is a novel water-soluble forskolin derivative that improves cardiac failure mainly through its beneficial effects on diastolic cardiac function. NKH477 is a potent activator of adenylyl cyclase and increases intracellular cAMP. NKH477 exerts an antiproliferative effect in vivo with an altered cytokine profile to inhibit the acute rejection of rat orthotopic lung allografts[1].
CSN22872 KH7 330676-02-3 KH 7 is a selective soluble adenylyl cyclase inhibitor.
CSN11051 (3R,4aR,5S,6S,6aS,10S,10aR,10bS)-6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-3-vinyldodecahydro-1H-benzo[f]chromen-5-yl acetate 66575-29-9 Forskolin is a ubiquitous activator of eukaryotic adenylyl cyclase (AC) in a wide variety of cell types with binding (IC50=41 nM) to and activation (EC50=0.5 μM) of type I adenylyl cyclase. It is commonly used to raise levels of cAMP in the research of cell physiology.
CSN20413 CB-7921220 115453-99-1 CB7921220 is an inhibitor of adenylyl cyclase isoform-1 (AC1) and isoform-6 (AC6).
CSN22739 Rp-cAMPS triethylammonium salt 151837-09-1 cAMPS-Rp, Triethylammonium Salt acts as a competitive antagonist of cAMP-induced activation of PKA (IC50 = 11 - 16 μM) by interacting with cAMP binding sites on the regulatory subunits.
CSN10469 6,6'-Thiobis(2,4-dichlorophenol) 97-18-7 Bithionol is an anti-parasitic drug and can be used to inhibit solid tumor growth in several preclinical cancer models.
CSN25537 ((2S,5R)-5-(6-Amino-9H-purin-9-yl)tetrahydrofuran-2-yl)methanol 4097-22-7 2′,3′-Dideoxyadenosine is a nucleoside analog of deoxyadenosine. It inhibits adenylyl cyclase and may play a key role in the inhibition of tumor progression. It is a potent inhibitor of reverse transcriptase enzyme of HIV.
CSN27244 2',5'-Dideoxyadenosine   6698-26-6 2',5'-Dideoxyadenosine is a potent and non-competitive adenylyl cyclase inhibitor via binding the P-site with an IC50 of 3 µM . 2',5'-Dideoxyadenosine is a nucleoside analog and exerts a potent antiadrenergic action in heart .
CSN19770 14-Deoxyandrographolide 4176-97-0 14-Deoxyandrographolide, a natural product isolated and purified from the herbs of Andrographis paniculata (Burm.
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