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118525-40-9

中文名称 去水淫羊藿黄素
英文名称 ICARITIN
CAS 118525-40-9
分子式 C21H20O6
分子量 368.38
MOL 文件 118525-40-9.mol
更新日期 2024/05/27 17:16:45
118525-40-9 结构式 118525-40-9 结构式

基本信息

中文别名
淫羊藿黄素
三七淫羊藿素
脱水淫羊藿黄素
去水淫羊藿黄素
淫羊藿素(标准品)
去水淫羊藿黄素, >98%
淫羊藿苷杂质2(脱水淫羊藿素)
去水淫羊藿黄素(G级现货,剩余原料)
ANHYDROICARITIN 脱水淫羊藿素
ANHYDROICARITIN 脱水淫羊藿素 标准品
英文别名
ICARITIN
Icaritin>
Icaritin, >98%
Icaritin(Anhydroicaritin)
Icariin Impurity 2 (Icaritin)
3,7-bis(2-hydroxyethyl)icaritin
3,5,7-trihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one
3,5,7-Trihydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one
4H-1-Benzopyran-4-one,3,5,7-trihydroxy-2-(4-methoxyphenyl)-8-(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

外观性状黄色结晶粉末,可溶于甲醇、乙醇、DMSO等有机溶剂,来源于淫羊藿。
熔点239℃
沸点582.0±50.0 °C(Predicted)
密度1.359
闪点206.7℃
储存条件2-8°C
溶解度DMSO:可溶5mg/mL,澄清(加热)
酸度系数(pKa)6.44±0.40(Predicted)
形态粉末
颜色淡黄色至深黄色
最大波长(λmax)368nm(MeOH)(lit.)
InChIInChI=1S/C21H20O6/c1-11(2)4-9-14-15(22)10-16(23)17-18(24)19(25)20(27-21(14)17)12-5-7-13(26-3)8-6-12/h4-8,10,22-23,25H,9H2,1-3H3
InChIKeyTUUXBSASAQJECY-UHFFFAOYSA-N
SMILESC1(C2=CC=C(OC)C=C2)OC2=C(C/C=C(/C)\C)C(O)=CC(O)=C2C(=O)C=1O

应用领域

用途1
具有降压,抗放射性软组织损伤的作用。

安全数据

WGK Germany3
RTECS号DJ3100870
海关编码29329990

常见问题列表

生物活性
Icaritin (Anhydroicaritin) 是 Epimedium Genusis 的异戊二烯类黄酮衍生物,有效抑制 K562 细胞 (IC50 为 8 µM) 和原代 CML 细胞 (对 CML-CP 的 IC50 值为 13.4 µM,对 CML-BC 的 IC50 值为 18 µM) 的增殖。Icaritin 可以调节 MAPK/ERK/JNK 和 JAK2/STAT3/AKT 信号传导,并具有增强成骨的作用。
体外研究

Icaritin (4-64 µM; 48 hours; K562, imatinib-resistant cells and primary CML cells) treatment inhibits proliferation of K562, imatinib-resistant cells and primary CML cells .
Icaritin (0-64 µM; 48 hours; K562 and primary cells) treatment induces K562 or primary cells apoptosis in an concentration dependent manner.
Icaritin (32 µM; K562 cells) treatment increases cell population in the sub-G1 phase in K562 cells.
Icaritin (0-64 µM; 48 hours; K562 cells) treatment inhibits MAPK/ERK/JNK downstream signaling and diminishes Jak2/Stat3/Akt expression. Icaritin treatment also significantly inhibits Bcl-2 protein expression and up-regulated Bax protein expression in K562 with a dose-dependent manner accompanied by the cleavage activation of caspase-3 or caspase-9, and a down-regulated expression of Apaf-1.

Cell Proliferation Assay

Cell Line: K562, imatinib-resistant cells and primary CML cells
Concentration: 4 µM, 8 µM, 16 µM, 32 µM and 64 µM
Incubation Time: 48 hours
Result: Inhibited cell proliferation.

Apoptosis Analysis

Cell Line: K562 or primary cells
Concentration: 0 µM, 4 µM, 8 µM, 16 µM, 32 µM and 64 µM
Incubation Time: 48 hours
Result: Induced K562 or primary cells apoptosis.

Cell Cycle Analysis

Cell Line: K562 cells
Concentration: 32 µM
Incubation Time:
Result: Cell population in the sub-G1 phase was increased.

Western Blot Analysis

Cell Line: K562 cells
Concentration: 0 µM, 4 µM, 8 µM, 16 µM, 32 µM and 64 µM
Incubation Time: 48 hours
Result: Inhibited MAPK/ERK/JNK downstream signaling and diminishes Jak2/Stat3/Akt expression.
体内研究

Icaritin (4-8 mg/kg; intraperitoneal injection; daily; for 10 weeks; female NOD-SCID nude mice) treatment could prolong lifespan of NOD-SCID nude mice inoculated with K562 cells without suppression of bone marrow in mouse leukemia model.

Animal Model: Female NOD-SCID nude mice (6-8 weeks old) with K562 cells
Dosage: 4 mg/kg and 8 mg/kg
Administration: Intraperitoneal injection; daily; for 10 weeks
Result: Could prolong lifespan of NOD-SCID nude mice inoculated with K562 cells without suppression of bone marrow.
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