255730-18-8
255730-18-8 结构式
基本信息
中文别名
青蒿酮 英文别名
ArtemisoneArtemifone
BAY 44-9585
YHVQDGXHTCSGBJ-AKSSTEKGSA-N
10alpha-[4'-(S,S-Dioxothiomorpholin-1'-yl)]-10-deoxodihydroartemisinin
4-[(3R,5aS,6R,8aS,9R,10R,12R,12aR)-decahydro-3,6,9-trimethyl-3,12-epoxy-12H-pyrano[4,3-j]-1,2-benzodioxepin-10-yl]thiomorpholine 1,1-dioxide
Thiomorpholine, 4-[(3R,5aS,6R,8aS,9R,10R,12R,12aR)-decahydro-3,6,9-trimethyl-3,12-epoxy-12H-pyrano[4,3-j]-1,2-benzodioxepin-10-yl]-, 1,1-dioxide
物理化学性质
沸点536.5±50.0 °C(Predicted)
密度1.33±0.1 g/cm3(Predicted)
储存条件-20°C储存
溶解度DMSO : 130 mg/mL (323.77 mM)
酸度系数(pKa)2.99±0.20(Predicted)
常见问题列表
生物活性
Artemisone (Artemifone) 是一种有效、半合成的抗疟疾剂，能够抑制多种 P. falciparum，平均 IC50 值为 0.83 nM。Artemisone 还是一种人 CMV 的有效抑制剂。靶点
IC50: 0.83 nM ( P. falciparum )
体外研究
Artemisone inhibits 3D7 and K1 P. falciparum , with IC 50 s of 0.88±0.59 and 1.23±0.64 nM, respectively.
体内研究
Artemisone is effectve at inhibiting the parasitaemia in the
P. berghei
NY susceptible strain, with an ED
50
of 9.62 mg/kg via subcutaneous route and 11.67 mg/kg via oral administration.
Artemisone (3, 1, 0.3 and 0.1 mg/kg, s.c.) in combination with ohter antimalarials has enhanced effect against the chloroquine-resistant line
P. yoelii
NS