Avanafil

製品コードS4019 バッチS401901

印刷

化学情報

 Chemical Structure Synonyms N/A Storage
(From the date of receipt)
3 years -20°C powder
1 years -80°C in solvent
化学式

C23H26ClN7O3

分子量 483.95 CAS No. 330784-47-9
Solubility (25°C)* 体外 DMSO 97 mg/mL (200.43 mM)
Water Insoluble
Ethanol Insoluble
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

溶剤液(一定の濃度)を調合する

生物活性

製品説明 Avanafil is a highly selective PDE5 inhibitor with IC50 of 5.2 nM, >121-fold selectivity over other PDEs.
in vivo Avanafil (i.v.) potentiates penile tumescence with ED200% of 37.5 μg/kg in dogs. Furthermore, intraduodenal treatment of Avanafil potentiates pelvic nerve stimulation induced changes in intracavernous pressure and duration. [1] The cavernous injection of avanafil (1 μM) in T2DM rats results in partial improvement in erectile responses. [2]
特徴 Highly selective for PDE5.

プロトコル(参考用のみ)

キナーゼアッセイ PDE Assay
PDE1, 2, 3, 4, 5 and 6 activity is assayed using 1 μM cGMP, 1 μM cGMP, 1 μM cAMP, 1 μM cAMP, 1 μM cGMP and 10 μM cGMP, respectively, as the substrate. PDE7, 8, 9, 10 and 11 activity is assayed using 0.1 μM cAMP, 0.05 μM cAMP, 0.05 μM cGMP, 0.25 μM cAMP and 1 μM cGMP, respectively, as the substrate. PDE assay is done by the radiolabeled nucleotide method.7 PDE enzyme (100 μl) in 50 mM Tris-HCl (pH 8.) is added to 200 μl assay buffer composed of 50 mM Tris-HCl (pH 8.0), 12.5 mM MgCl2, 10 mM 2-mercaptoethanol and 0.825 mg/ml bovine serum albumin. The enzyme reaction is started by adding 200 μl substrate solution containing [3H]cGMP plus unlabeled cGMP or [3H]cAMP plus unlabeled cAMP in 50 mM Tris-HCl (pH 8.0). Reaction mixtures are incubated at 37C for 30 minutes and then boiled for 1.5 minutes. Subsequently 100 μl 1 mg/ml Crotalus atrox snake venom are added and incubated at 37C for 30 minutes. The reaction is stopped by adding 500 μl methanol. Resultant solutions are applied to a Dowex (1 × 8, 200 to 400) column (volume 0.225 ml). Eluate radioactivity is measured with 5 ml aqueous scintillation cocktails. DMSO solution without the compounds served as a control. The final concentration of DMSO in the reaction mixture is 1% volume per volume.
動物実験 動物モデル Male mongrel dogs
投薬量 1-300 μg/kg
投与方法 Intraduodenal treatment or i.v.

Selleckの高級品が、幾つかの出版された研究調査結果(以下を含む)で使われた:

c-FOS drives reversible basal to squamous cell carcinoma transition [ Cell Rep, 2021, 37(1):109774] PubMed: 34610301

長期の保管のために-20°Cの下で製品を保ってください。

人間や獣医の診断であるか治療的な使用のためにでない。

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