Avanafil(TA-1790)

产品编号: DC8799 Featured
Avanafil(TA-1790)
结构式
330784-47-9
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中国地区超过5000个高品质化合物库存
应用领域
Avanafil(TA-1790)是高活性PDE-5抑制剂,IC50为5.2 nM,对PDE1,PDE6和PDE11活性较低。
Cas No.: 330784-47-9
名称:
别名:
SMILES: C(N1CCC[C@@H]1CO)1=NC=C(C(=O)NCC2=NC=CC=N2)C(NCC2=CC=C(OC)C(Cl)=C2)=N1
分子式: C23H26ClN7O3
分子量: 483.95
纯度:
保存条件: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description:
In Vivo:
In Vitro:
References: Avanafil is highly selective toward PDE5 and against all other PDE isozymes tested. Lower selectivity against PDE1, PDE6, and PDE11 is consistent with results from randomized, placebo-controlled, phase 3 trials in which musculoskeletal and hemodynamic adverse events were reported in <2% of patients and no color vision-related abnormalities were reported with avanafil doses up to 200mg once daily . Intraduodenal doses of avanafil or sildenafil (0.1 and 1 mg/kg) potentiated the AUC of nitroglycerin induced hypotension. However, the potentiating effect of avanafil at 1 mg/kg was significantly weaker than that of sildenafil (p <0.05)
Kinase Assay:
Cell Assay:
Animal Administration:
References:
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
产品编号 产品名称 应用领域
DC8799 Avanafil(TA-1790) Avanafil(TA-1790)是高活性PDE-5抑制剂,IC50为5.2 nM,对PDE1,PDE6和PDE11活性较低。