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PDE

PDE

As fosfodiesterases (PDEs) são enzimas que hidrolisam nucleotídeos cíclicos, como AMPc e GMPc, em suas formas inativas, desempenhando um papel crucial na regulação das vias de sinalização intracelular. Inibidores de PDE são utilizados no tratamento de diversas condições, incluindo doenças cardiovasculares, disfunção erétil e distúrbios respiratórios, devido à sua capacidade de modular os níveis de nucleotídeos cíclicos. Na CymitQuimica, oferecemos uma variedade de inibidores de PDE para apoiar sua pesquisa em sinalização celular, farmacologia e desenvolvimento terapêutico.

Foram encontrados 188 produtos para "PDE".

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  • Z21115

    CAS:
    Z21115 is an orally effective phosphodiesterase 4 (PDE4) inhibitor that can inhibit PDE4D7 with an IC50 of 10.5 nM. It suppresses the expression of IL-6, TNF-α, and iNOS induced by Lipopolysaccharide. In a DSS-induced mouse colitis model, Z21115 demonstrates anti-inflammatory activity without significant toxicity at doses up to 1 g/kg.
    Fórmula:C20H20F2N2O4
    Peso molecular:390.38

    Ref: TM-T89970

    10mg
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    50mg
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  • GSK4394835A

    CAS:
    GSK4394835A is a reversible covalent inhibitor of PDE3B, with a pIC50 of 6.2. This compound is useful for research in cardiovascular diseases.
    Fórmula:C27H26BN3O6
    Peso molecular:499.33

    Ref: TM-T214298

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    50mg
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  • Ensifentrine tosylate

    CAS:
    Ensifentrine (RPL-554) tosylate is an inhaled dual inhibitor of PDE3 and PDE4, with IC50 values of 0.4 nM and 1479 nM, respectively. By blocking these enzymes, it increases the levels of cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) in lung cells, leading to bronchodilation and inhibition of inflammatory cell activation and migration. Ensifentrine tosylate is used in the study of chronic obstructive pulmonary disease (COPD).
    Fórmula:C33H39N5O7S
    Peso molecular:649.76

    Ref: TM-T214818

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  • LT-104A

    CAS:
    LT-104A is a potent PDE4 inhibitor that elevates intracellular cAMP levels (EC50 = 1.9 μM) and inhibits PDE4D3 activity (IC50 = 9.3 μM). It activates the cAMP-PKA-CREB anti-inflammatory pathway and suppresses NF-κB-related gene expression (Il1b and Nos2), making it applicable for research in inflammation-related diseases.
    Fórmula:C33H34O7
    Peso molecular:542.63

    Ref: TM-T214052

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  • PDE5-IN-15

    CAS:
    PDE5-IN-15 (compound 21) is a xanthine derivative and PDE5 inhibitor with IC50 values of 0.002 μM for hPDE5, 0.180 μM for bPDE6, 2.85 μM for bPDE1, and 2.22 μM for hPDE3. It exhibits good oral bioavailability in dogs and is applicable in research related to male erectile dysfunction.
    Fórmula:C21H23N5O3
    Peso molecular:393.44

    Ref: TM-T212472

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  • PDE11A modulator-1

    CAS:
    PDE11A modulator-1 is a regulator of PDE11A.
    Fórmula:C20H16N4O2
    Peso molecular:344.37

    Ref: TM-T214751

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  • PF-00489791

    CAS:
    PF-00489791 (PF4634817) is a long-acting PDE5 inhibitor with hypotensive activity for the study of diabetic nephropathy.
    Fórmula:C20H28N8O4S
    Pureza:99.97%
    Cor e Forma:Yellow Solid
    Peso molecular:476.55

    Ref: TM-T28360

    1mg
    34,00€
    5mg
    62,00€
    10mg
    100,00€
    25mg
    268,00€
  • Vizenpistat

    CAS:
    Vizenpistat is an ENPP1 inhibitor utilized in tumor research.
    Fórmula:C15H21N5O4S
    Cor e Forma:Solid
    Peso molecular:367.42

    Ref: TM-T211655

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    50mg
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