- 英文名称
- Cirsimarin
- 分子式
- C23H24O11
- 分子量
- 476.43
- 中文别名
- 滨蓟黄苷; 5-羟基-6,7-二甲氧基-2-(4-(((2S,3R,4S,5S,6R)-3,4,5-三羟基-6-(羟甲基)四氢-2H-吡喃-2-基)氧基)苯基)-4H-苯并吡喃-4-酮; 化合物T10822; Cirsitakaoside; cirsimartin; 5-hydroxy-6,7-dimethoxy-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one; 2-(4-(beta-D-Glucopyranosyloxy)phenyl)-5-hydroxy-6,7-dimethoxy-4H-1-benzopyran-4-one; 2-[4-(beta-D-Glucopyranosyloxy)phenyl]-5-hydroxy-6,7-dimethoxy-4H-1-benzopyran-4-one; 5-hydroxy-6,7-dimethoxy-2-(4-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxyphenyl)chromen-4-one; Cirsimaretin; Cirsimaritin 4'-glucoside; 5-hydroxy-6,7-dimethoxyflavone-4'-glucoside; 5,4'-Dihydroxy-6,7-dimethoxyflavone 4'-O-beta-D-glucoside; 4-(5-Hydroxy-6,7-dimethoxy-4-oxo-4H-chromen-2-yl)phenyl β-D-glucopyranoside; Cirsimarine
- 用途
- 生命科学；- 生物活性：Cirsimarin 是一种从 Microtea debilis 中分离出来的有效的抗脂类黄酮，具有有效的抗脂肪作用，并能减少小鼠脂肪组织的沉积。其脂解活性是由于对腺苷 A1 受体的拮抗活性及其对磷酸二酯酶 (phosphodiesterase) 的抑制作用。- 靶点：Phosphodiesterase；Adenosin A1 receptor
