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4449-55-2

中文名称 WARANGALONE
英文名称 warangalone
CAS 4449-55-2
分子式 C25H24O5
分子量 404.46
MOL 文件 4449-55-2.mol
更新日期 2024/08/26 15:19:02
4449-55-2 结构式 4449-55-2 结构式

基本信息

中文别名
攀登鱼藤异黄酮
英文别名
warangalone
Scandenolone
Warangalone (Scandenolone)
5-hydroxy-7-(4-hydroxyphenyl)-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-g]chromen-6-one
5-hydroxy-7-(4-hydroxyphenyl)-2,2-dimethyl-10-(3-methylbut-2-enyl)-6-pyrano[3,2-g][1]benzopyranone
2H,6H-Benzo[1,2-b:5,4-b']dipyran-6-one,5-hydroxy-7-(4-hydroxyphenyl)-2,2-dimethyl-10-(3-methyl-2-buten-1-yl)-
所属类别
天然产物:黄酮类化合物

物理化学性质

熔点164-165 °C
沸点627.0±55.0 °C(Predicted)
密度1.258±0.06 g/cm3(Predicted)
储存条件-20°C储存
溶解度溶于二甲基亚砜
酸度系数(pKa)6.39±0.40(Predicted)
形态Solid
颜色Light yellow to yellow
WARANGALONE价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/08/19HY-N1074WARANGALONE
Warangalone
4449-55-21mg3341元

常见问题列表

生物活性
Warangalone 是抗疟疾化合物,能够抑制 3D7 (氯喹敏感) 和 K1 (氯喹耐药) 寄生虫的生长, IC50 值分别为 4.8 μg/mL 和 3.7 μg/mL。 Warangalone 还可以抑制环 AMP 依赖性蛋白激酶催化亚基 (cAK),其 IC50 值为 3.5 μM。
靶点

IC50: 4.8 μg/mL (3D7), 3.7 μg/mL (K1)
IC50: 3.5 μM (cAK)

体外研究

Warangalone is an anti-malarial compound which can inhibit the growth of both strains of parasite 3D7 (chloroquine sensitive) and K1 (chloroquine resistant) with IC 50 s of 4.8 μg/mL and 3.7 μg/mL, respectively. Warangalone can also inhibit cyclic AMP-dependent protein kinase catalytic subunit (cAK) with an IC 50 of 3.5 μM. When HL-60 cells are exposed to Warangalone (30 μM) for 24 h, Warangalone induces a significant decrease (8%) in cell viability compare to controls. Warangalone also inhibits HL-60 cell growth within 24 h in a time-dependent fashion. A time-dependent increase in caspase-9 activity is observed in Warangalone-treated cells.

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