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Cyclic Nucleotides

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  • 8-pCPT-2-O-Me-cAMP-AM | Epac activator
    8-pCPT-2-O-Me-cAMP-AM | Epac activator
    $148.00
    8-pCPT-2-O-Me-cAMP-AM (1152197-23-3) is a potent, cell-permeable Epac (exchange protein directly activated by cAMP) activator.1 Induces RAP1 activation and insulin secretion in pancreatic beta cell lines...

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  • Amiodarone HCl | PDE inhibitor
    Amiodarone HCl | PDE inhibitor
    $45.00
    Amiodarone HCl (19774-82-4) is a pan-specific inhibitor of phosphodiesterases (IC50=2-50 μM). Inhibition of PDEs leads to increased concentration of intracellular cAMP which activates PKA2. Does not inhibit PDE8 or PDE93...

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  • Focus Biomolecules cell signaling reagent supplier, chemical structure of BC-11-38 | PDE-11 inhibitor | CAS 686770-80-9
    BC-11-38 | PDE-11 inhibitor
    $90.00
    A potent and selective inhibitor of phosphodiesterase PDE11 (IC50=0.28 mM).1  IC50s for PDE1-10 are greater than 100 mM. Restores the ability of p54nrb / NONOKD cells to generate cAMP in response to ACTH stimulation and...

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  • BML-288 | 851-55-3 | Structure | Supplier
    BML-288 | PDE2 inhibitor
    $55.00
    BML-288 (851-55-3) is a potent and selective inhibitor of phosphodiesterase PDE2, IC50 = 40 nM. More potent than EHNA, another commonly used PDE2 inhibitor. Displays no effect on a panel of over 80 receptors, ion channels...

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  • Focus Biomolecules cell signaling reagent supplier, chemical structure of BRL-50481 | PDE7 inhibitor | CAS 433695-36-4
    BRL-50481 | PDE7 inhibitor
    $60.00
    BRL-50481 (433695-36-4) is a potent and selective inhibitor of phosphodiesterase-7 (PDE7), Ki=180 nM.1 Induces apoptosis in chronic lymphocytic leukemia cells which express PDE7B.2 BRL-50481 increases...

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  • Cilostamide | PDE3 inhibitor
    Cilostamide | PDE3 inhibitor
    $60.00
    Cilostamide (68550-75-4) is a selective inhibitor of phosphodiesterase-3 (PDE3). Displays limited selectivity for PDE3A versus PDE3B (IC50 = 27 and 50 nM)1,2. Blocks PKB/Akt signaling pathway downstream via inhibition of...

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  • Focus Biomolecules cell signaling reagent supplier, chemical structure of Cilostazol | PDE3A inhibitor | CAS 73963-72-1
    Cilostazol | PDE3A inhibitor
    $60.00
    Cilostazol (73963-72-1) is a clinically approved phosphodiesterase III (PDE3) inhibitor (IC50 = 0.2 μM) and anti-thrombotic agent. It inhibits platelet aggregation and is a direct arterial vasodilator...

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  • Dipyridamole | 58-32-2 | Structure | Supplier
    Dipyridamole | Pan-specific PDE inhibitor
    $22.00
    Dipyridamole (58-32-2) is a phosphodiesterase inhibitor (IC50=0.37, 0.38, 0.45, 0.9 and 4.5 μM for PDE11, 6, 10, 5 and 8 respectively.1,2 Potent equilibrative nucleoside transporter 1 (ENT1) inhibitor Ki=8.2 nM vs. 144.8...

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  • EPAC 5376753 | Structure | Supplier
    EPAC 5376753 | EPAC inhibitor
    $60.00
    EPAC 5376753 is an allosteric inhibitor of Epac1, IC50= 4 μM.1 Does not inhibit PKA or adenylyl cyclase. Inhibits biological functions mediated by Epac including cAMP-induced increase in migration of cardiac fibroblasts...

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  • Focus Biomolecules supplier, chemical structure of Forskolin | Adenylate cyclase activator | CAS 66575-29-9
    Forskolin | Adenylate cyclase activator
    $60.00
    Forskolin (66575-29-9) is a widely used adenylate cyclase activator.1 Forskolin also is a positive inotropic agent, vasodilator and induces platelet activation among other activities.2-5 References/Citations1) Awad et al...

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  • Focus Biomolecules cell signaling reagent supplier, chemical structure of IBMX | PDE inhibitor | CAS 28822-58-4
    IBMX | PDE inhibitor
    $30.00
    IBMX (28822-58-4) is a pan-specific inhibitor of phosphodiesterases (IC50=2-50 µM). Inhibition of PDEs leads to increased concentration of intracellular cAMP which activates PKA2. IBMX does not inhibit PDE8 or PDE93...

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  • Ibudilast | Neuroinflammation inhibitor
    Ibudilast | Neuroinflammation inhibitor
    $40.00
    Phosphodiesterase inhibitor with some selectivity for PDE4 and 5. (IC50s= 53, 35, 48, 12 and 10 μM for PDE 1a, 2, 3, 4 and 5 respectively1). Acts as a cerebral vasodilator by selectively inducing a cGMP-independent...

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  • Focus Biomolecules supplier, chemical structure of Mycophenolate mofetil | Immunomodulator | CAS 128794-94-5
    Mycophenolate mofetil | Immunomodulator
    $35.00
    Mycophenolate mofetil (128794-94-5) is a mycophenolic acid prodrug. Immunosuppressive agent useful in prevention of organ allograft rejection.1 Is metabolized to mycophenolic acid in vivo  which acts by inhibiting...

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  • Focus Biomolecules supplier, chemical structure of Mycophenolic acid | Immunosuppressant | CAS 24280-93-1
    Mycophenolic acid | Immunosuppressant
    $40.00
    Mycophenolic acid (24280-93-1) is an immunomodulator1 that blocks the biosynthesis of guanine nucleotides via inhibition of inosine 5'-monophosphate dehydrogenase. This in turn suppresses the production of proinflammatory...

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  • Focus Biomolecules supplier, chemical structure of NKY-80 | Adenylate cyclase inhibitor | CAS 299442-43-6
    NKY-80 | Adenylate cyclase inhibitor
    $58.00
    NKY-80 (299442-43-6) is a potent and selective adenylyl cyclase inhibitor. Selective for AC5 and over AC3 and AC2 (IC50 = 8.3 μM, 132 μM and 1.7 mM respectively)1,2. More recently shown to indiscriminantly inhibit AC63...

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  • Focus Biomolecules cell signaling reagent supplier, structure of Resveratrol | Antioxidant/SIRT1 activator | CAS 201-36-0
    Resveratrol | Antioxidant/SIRT1 activator
    $45.00
    Resveratrol (501-36-0) is a naturally occurring phenolic antioxidant. Displays antitumor and antiplatelet effects1. Activates SIRT1 and increases longevity in yeast2. Resveratrol ameliorates ageing-related phenotypes by...

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  • Focus Biomolecules cell signaling reagent supplier, structure of Ro 13-6438 | Quazinone | PDE3 inhibitor | CAS 70018-51-8
    Ro 13-6438 | PDE3 inhibitor
    $75.00
    Ro 13-6438 (70018-51-8) is a selective inhibitor of phosphodiesterase III (PDE III, IC50 = 0.6 μM). References/Citations1) Eigenmann et al. (1984) Cardiovascular profile of Ro 13-6438, a novel positive inotropic agent...

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  • Focus Biomolecules cell signaling reagent supplier, chemical structure of RO 20-1724 | PDE4 inhibitor | CAS 28825-17-5
    RO 20-1724 | PDE4 inhibitor
    $45.00
    RO 20-1724 (29925-17-5) is a selective inhibitor of cAMP-specific phosphodiesterase (PDE4), IC50 = 0.2 μM. Displays anti-inflammatory activity. Cell permeable References/Citations1) Soderling et al. (1998), Cloning and...

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  • Focus Biomolecules cell signaling reagent supplier, chemical structure of Rolipram | PDE4 inhibitor | CAS 61413-54-5
    Rolipram | PDE4 inhibitor
    $60.00
    Rolipram (61413-54-5) is a selective inhibitor of cAMP-specific phosphodiesterase (PDE4), IC50 = 1 μM. Displays beneficial effects in neurodegenerative diseases. Rolipram also displays anti-inflammatory activity and...

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  • STF034307 | Structure | Supplier
    ST-034307 | Adenylate cyclase 1 inhibitor, analgesic activity
    $60.00
    ST-034307 (133406-29-8) is a novel selective adenylyl cyclase 1 (AC1) inhibitor, IC50=2.3 μM. Inhibits calcium2+-stimulated cAMP accumulation in HEK cells stably transfected with AC1.1 It was also shown to inhibit...

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