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Merck
CN

SML0551

淫羊藿素

≥98% (HPLC)

别名:

3,5,7-三羟基-2-（4-甲氧苯基）-8-（3-甲基-2-丁烯-1-基）-4H-1-苯并吡喃-4-酮

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关于此项目

经验公式（希尔记法）:
C21H20O6
化学文摘社编号:
118525-40-9
分子量:
368.38
NACRES:
NA.77
PubChem Substance ID:
329825547
UNSPSC Code:
12352200
MDL number:
MFCD22422519

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产品名称

淫羊藿素, ≥98% (HPLC)

InChI

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

SMILES string

COc1ccc(cc1)C2=C(O)C(=O)c3c(O)cc(O)c(C\C=C(\C)C)c3O2

InChI key

TUUXBSASAQJECY-UHFFFAOYSA-N

assay

≥98% (HPLC)

form

powder

color

light yellow to dark yellow

solubility

DMSO: 5 mg/mL, clear (warmed)

storage temp.

2-8°C

Quality Level

100

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Biochem/physiol Actions

淫羊藿素促进间充质干细胞 (MSCs) 的成骨细胞分化，同时抑制 MSCs 的成脂分化。
淫羊藿素增强间充质干细胞 (MSCs) 的成骨细胞分化。可能具有类雌激素活性。
淫羊藿素是从淫羊藿中分离得到的一种淫羊藿黄酮成分，它通过抑制 PPAR-g 通路促进间充质干细胞 (MSCs) 向成骨细胞分化，同时抑制 MSCs 的成脂分化。淫羊藿素对 MSCs 增殖无影响。此外，淫羊藿素最有可能通过调节 MAPK/ERK/JNK 和 JAK2/STAT3/AKT 信号，有效抑制慢性髓样白血病 (CML) 和乳腺癌细胞增殖。淫羊藿素与其它黄酮类化合物一样，可能具有雌激素样活性。

Features and Benefits

《受体分类和信号转导》手册的 JAK、MAPK 和 核受体（PPAR） 页面有该化合物的介绍。想要浏览手册的其他页面， 请单击此处。

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000161289
0000161289
0000161290
0000129556

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Haibang Hao et al.
European journal of immunology, 49(12), 2235-2244 (2019-08-30)
Icaritin, a hydrolytic product of icariin isolated from traditional Chinese herbal medicine genus Epimedium, has many pharmacological and biological activities. Here, we show that icaritin can effectively decrease tumor burden of murine B16F10 melanoma and MC38 colorectal tumors in a
Jian feng Zhu et al.
PloS one, 6(8), e23720-e23720 (2011-09-03)
To explore the effects of Icaritin on chronic myeloid leukemia (CML) cells and underlying mechanisms. CML cells were incubated with various concentration of Icaritin for 48 hours, the cell proliferation was analyzed by MTT and the apoptosis was assessed with
Dong Yao et al.
PloS one, 7(8), e41264-e41264 (2012-09-07)
We found that Icaritin, an intestinal metabolite of Epimedium-derived flavonoids (EF) enhanced osteoblastic differentiation of mesenchymal stem cells (MSCs) only under osteogenic induction conditions. We also demonstrated its effect on inhibition of adipogenic differentiation of MSCs. Unlike the findings of
Hongchao Li et al.
Journal of cellular biochemistry (2018-11-06)
Glioblastoma (GBM) is a common and aggressive brain tumor that is associated with significant increase in glycolysis for energy production. Icaritin is a natural compound and exhibits anticancer activity in GBM. However, the effect of icaritin on glycolysis in GBM
Jing-Shan Tong et al.
PloS one, 6(3), e16781-e16781 (2011-03-17)
Icaritin, a compound from Epimedium Genus, has selective estrogen receptor (ER) modulating activities, and possess anti-tumor activity. Here, we examined icaritin effect on cell growth of human endometrial cancer Hec1A cells and found that icaritin potently inhibited proliferation of Hec1A
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