Siguazodan

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

Siguazodan 是一种有效的、选择性的、口服活性的磷酸二酯酶 III ((PDE-III)) 抑制剂，IC50 为 117 nM。

Siguazodan is an effective, selective, orally active phosphodiesterase III ((PDE-III)) inhibitor with an IC50 of 117 nM. Siguazodan inhibited phenylephrine induced 5-HT release with an IC50 value of 4.2 μM。 Siguazodan can increase cAMP accumulation in intact platelets, with EC50 of 18.88 μM.(In Vitro):Siguazodan increases cAMP accumulation in intact platelets with an EC50 of 18.88 μM. Siguazodan also inhibits phenylephrine-induced 5-HT release with an IC50 value of 4.2 μM. In platelet-rich plasma (PRP), Siguazodan inhibits U46619-induced aggregation more potently than that induced by adenosine 5'-diphosphate (ADP), and collagen. Treatment of the PRP with Aspirin has no effect on the potency of Siguazodan. In washed platelets, Siguazodan increases cyclic AMP levels and reduces cytoplasmic free calcium. ADP decreases the ability of Siguazodan to raise cyclic AMP and this may explain its lower potency in inhibiting responses to ADP.(In Vivo):Siguazodan has positive inotropic and vasodilating actions in various laboratory animals and is orally active with a long duration of action in conscious dogs.

Siguazodan selectively inhibits the major cyclic AMP-hydrolysing PDE in human platelet supernatants. The inhibited enzyme has been variously termed cyclic GMP-inhibited PDE or PDE-III. In platelet-rich plasma (PRP), Siguazodan inhibits U46619-induced aggregation more potently than that induced by adenosine 5'-diphosphate (ADP), and collagen. Treatment of the PRP with Aspirin has no effect on the potency of Siguazodan. In washed platelets, Siguazodan increases cyclic AMP levels and reduces cytoplasmic free calcium. ADP decreases the ability of Siguazodan to raise cyclic AMP and this may explain its lower potency in inhibiting responses to ADP.Siguazodan has anti-platelet actions over the same concentration range that it is an inotrope and vasodilator.

Siguazodan is a potent, selective inhibitor of phosphodiesterase III that has positive inotropic and vasodilating actions in various laboratory animals and is orally active with a long duration of action in conscious dogs.

SKF 94836

Angiogenesis

PDE

GABA

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115344-47-3

284.323

C14H16N6O

>98% (HPLC)

In Vitro:?DMSO : 12.5 mg/mL (43.96 mM)

CN\C(NC#N)=N/c1ccc(cc1)C1=NNC(=O)CC1C

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(-20℃)

With Ice Pack

≥ 2 years