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Phosphodiesterase(PDE)

Phosphodiesterase(PDE)

Phosphodiesterase (PDE) is any enzyme that breaks a phosphodiester bond.When phosphodiesterase is mentioned, it usually refers to cyclic nucleotide phosphodiesterases, which are discussed below and have significant clinical implications. There are numerous other families of phosphodiesterases, however, including the phospholipases C and D, autotaxin, sphingomyelin phosphodiesterase, DNases, RNases, and restriction endonucleases, in addition to a large number of less well-studied small-molecule phosphodiesterases.A group of enzymes known as cyclic nucleotide phosphodiesterases breaks down the phosphodiester bond in the second messenger molecules cAMP and cGMP. Within subcellular domains, they control the cyclic nucleotide signaling's amplitude, duration, and localization. Therefore, PDEs play a crucial role in controlling the signal transduction process that these second messenger molecules mediate.

Phosphodiesterase(PDE) related products

Structure Cat No. Product Name CAS No. Product Description
Roflumilast-d4 N-Oxide (罗氟司特 d4 (N 氧化物)) V56170 Roflumilast-d4 N-Oxide (Roflumilast d4 (N-oxide)) 1794760-31-8 Roflumilast-d4 N-Oxide is the deuterium labelled form of Roflumilast.
S32826 V72082 S32826 1096770-84-1 S32826 is a potent autotaxin inhibitor (antagonist) with IC50 of 8.8 nM.
Sildenafil V4198 Sildenafil 139755-83-2 Sildenafil (formerly UK92480; UK-92480;Trade name: Revatio), the free base form of Sildenafil, is a potentandselective inhibitor of phosphodiesterase type 5 (PDE5) withIC50of 5.22 nM.
Sildenafil-d3 (UK-92480-d3) V72050 Sildenafil-d3 (UK-92480-d3) 1126745-90-1 Sildenafil-d3 is deuterium-labeled sildenafil.
Sildenafil-d3N-1 (UK-92480-d3N-1) V72087 Sildenafil-d3N-1 (UK-92480-d3N-1) 1126745-87-6 Sildenafil-d3-1 (UK-92480-d3-1) is deuterium-labeled sildenafil.
Sp-cAMPS sodium salt V69110 Sp-cAMPS sodium salt 142439-95-0 Sp-cAMPS sodium salt, a cAMP analog, is a potent cAMP-dependent activator of PKA I and PKA II.
Sp-cAMPS triethylamine V69116 Sp-cAMPS triethylamine 93602-66-5 Sp-cAMPS triethylamine, a cAMP analog, is a potent cAMP-dependent activator of PKA I and PKA II.
Tadalafil-d3 (IC-351-d3) V72065 Tadalafil-d3 (IC-351-d3) 960226-55-5 Tadalafil-d3 is the deuterium labelled form of Nortadalafil.
Theodrenaline hydrochloride ((±)-Theodrenaline hydrochloride) V72044 Theodrenaline hydrochloride ((±)-Theodrenaline hydrochloride) 2572-61-4 Theodrenaline HCl is a cardiotonic agent and is often mixed with Cafedrine in proportion to form Akrinor, which has a blood pressure lowering effect.
Thioquinapiperifil dihydrochloride (KF31327) V72026 Thioquinapiperifil dihydrochloride (KF31327) 204077-66-7 Thioquinapiperifil di-HCl (KF31327) is a specific, noncompetitive (IC50 of 0.074 nM) inhibitor of phosphodiesterase (PDE-5) for studies of sexual maturation.
THPP-1 V16347 THPP-1 1257051-63-0 THPP-1 is a novel, potent and orally bioavailable PDE10A (phosphodiesterase 10A) inhibitor withKi values of 1 nM and 1.3 nM for human and rat PDE10A, respectively.
TMX-4100 V72016 TMX-4100 2367619-63-2 TMX-4100 is a selective phosphodiesterase 6D (PDE6D) degrader.
Toddacumalone V72085 Toddacumalone 139750-79-1 Toddacoumalone is a natural phosphodiesterase 4 (PDE4) inhibitor (antagonist) with moderate potency and imperfect active molecule-like properties.
TPN729 V72034 TPN729 936951-20-1 TPN729 is a selective phosphodiesterase type 5 (PDE5) inhibitor (antagonist) with IC50 of 2.28 nM.
TPN729MA (TPN729 maleate) V72036 TPN729MA (TPN729 maleate) 1422955-52-9 TPN729MA (TPN729 maleate) is a selective phosphodiesterase type 5 (PDE5) inhibitor (antagonist) with IC50 of 2.28 nM.
Trequinsin hydrochloride (HL 725) V72011 Trequinsin hydrochloride (HL 725) 78416-81-6 Trequinsin HCl (HL 725) is a potent inhibitor of platelet CAMP phosphodiesterase (PDE) with IC50 of 0.25 nM.
Udenafil-d7 (Udenafil d7) V72045 Udenafil-d7 (Udenafil d7) 1175992-76-3 Udenafil-d7 is the deuterium labelled form of Udenafil.
Vardenafil HCl V31439 Vardenafil HCl 224785-91-5 Vardenafil HCl, also known as BAY 38-9456 HCl,is a novel and potent PDE inhibitor with IC50 of 0.7 and 180 nM for PDE5 and PDE1, respectively.
Vesnarinone (OPC8212) V27984 Vesnarinone (OPC8212) 81840-15-5 Vesnarinone (OPC-8212) is a quinolinone-based cardiotonic agent, acting as a mixed phosphodiesterase 3 (PDE3) inhibitor and ion-channel modifier with modest, dose-dependent, positive inotropic activity, but minimal negative chronotropic activity.
Vinpocetine-d5 (vinpocetine d5) V72037 Vinpocetine-d5 (vinpocetine d5) 2734920-39-7 Vinpocetine-d5 is the deuterium labelled form of Vinpocetine.
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