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118525-40-9

中文名稱 去水淫羊藿黃素
英文名稱 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 2025/01/07 18:51:24
118525-40-9 結(jié)構(gòu)式 118525-40-9 結(jié)構(gòu)式

基本信息

中文別名
淫羊藿黃素
三七淫羊藿素
脫水淫羊藿黃素
去水淫羊藿黃素
淫羊藿素(標(biāo)準(zhǔn)品)
去水淫羊藿黃素, >98%
淫羊藿苷雜質(zhì)2(脫水淫羊藿素)
去水淫羊藿黃素(G級(jí)現(xiàn)貨,剩余原料)
ANHYDROICARITIN 脫水淫羊藿素
ANHYDROICARITIN 脫水淫羊藿素 標(biāo)準(zhǔn)品
英文別名
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)-
所屬類別
天然產(chǎn)物:黃酮類化合物

物理化學(xué)性質(zhì)

外觀性狀黃色結(jié)晶粉末,可溶于甲醇、乙醇、DMSO等有機(jī)溶劑,來(lái)源于淫羊藿。
熔點(diǎn)239℃
沸點(diǎn)582.0±50.0 °C(Predicted)
密度1.359
閃點(diǎn)206.7℃
儲(chǔ)存條件2-8°C
溶解度DMSO:可溶5mg/mL,澄清(加熱)
酸度系數(shù)(pKa)6.44±0.40(Predicted)
形態(tài)粉末
顏色淡黃色至深黃色
最大波長(zhǎng)(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

應(yīng)用領(lǐng)域

用途1
具有降壓,抗放射性軟組織損傷的作用。

安全數(shù)據(jù)

WGK Germany3
RTECS號(hào)DJ3100870
海關(guān)編碼29329990

常見問題列表

生物活性
Icaritin (Anhydroicaritin) 是 Epimedium Genusis 的異戊二烯類黃酮衍生物,有效抑制 K562 細(xì)胞 (IC50 為 8 μM) 和原代 CML 細(xì)胞 (對(duì) CML-CP 的 IC50 值為 13.4 μM,對(duì) CML-BC 的 IC50 值為 18 μM) 的增殖。Icaritin 可以調(diào)節(jié) MAPK/ERK/JNK 和 JAK2/STAT3/AKT 信號(hào)傳導(dǎo),并具有增強(qiáng)成骨的作用。
體外研究

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.
體內(nèi)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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