Основные атрибуты  химическое свойство Информация о безопасности химические свойства, назначение, производство запасные части и сырье поставщик Обзор
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Icaritin

  • русский язык имя
  • английское имяIcaritin
  • CAS №118525-40-9
  • CBNumberCB2982508
  • ФормулаC21H20O6
  • мольный вес368.38
  • номер MDLMFCD22422519
  • файл Mol118525-40-9.mol
химическое свойство
Температура плавления 239℃
Температура кипения 582.0±50.0 °C(Predicted)
плотность 1.359
Fp 206.7℃
температура хранения 2-8°C
растворимость DMSO: soluble5mg/mL, clear (warmed)
форма powder
пка 6.44±0.40(Predicted)
цвет light yellow to dark yellow
λмакс 368nm(MeOH)(lit.)
InChI 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
ИнЧИКей TUUXBSASAQJECY-UHFFFAOYSA-N
SMILES C1(C2=CC=C(OC)C=C2)OC2=C(C/C=C(/C)\C)C(O)=CC(O)=C2C(=O)C=1O
FDA UNII UFE666UELY
UNSPSC Code 41116107
NACRES NA.77
Заявления об опасности и безопасности
WGK Германия 3
RTECS DJ3100870
кода HS 29329990

Icaritin химические свойства, назначение, производство

Химические свойства

Yellow crystalline powder, soluble in methanol, ethanol, DMSO and other organic solvents, derived from epimedium.

Использование

Icaritin is a hydrolytic product of Icariin, a traditional Chinese herbal medicine extracted from the Epimedium genus. Icaritin and Desmethylicaritin, is two metabolites of Icariin, dramatically inhibit the growth of most malignant cells. They also have significant antiangiogenesis properties, inhibiting or eliminating entirely the development of new malignant cells. Icaritin has been used in trials studying the treatment of Solid Tumors, Metastatic Breast Cancer, and Hepatocellular Carcinoma (HCC).

Синтез

The novel total synthesis of icaritin, naturally occurring with important bioactive 8-prenylflavonoid, was performed via a reaction sequence of 8 steps including Baker-Venkataraman reaction, chemoselective benzyl or methoxymethyl protection, dimethyldioxirane (DMDO) oxidation, O-prenylation, Claisen rearrangement and deprotection, starting from 2,4,6-trihydroxyacetophenone and 4-hydroxybenzoic acid in overall yields of 23%. The key step was Claisen rearrangement under microwave irradiation.
Total Synthesis of Icaritin via Microwave-assistance Claisen Rearrangement

Способ действия

Icaritin is a flavonoid first isolated from the Chinese herb H. epimedii that demonstrates anticancer activity against a variety of tumor cell lines. Icaritin was shown in vitro to sustain extracellular signal–regulated kinase (ERK) activity through stimulating estrogen receptors. Prolonged ERK activation arrested the cell cycle in the G2 stage and subsequently triggered apoptosis. It has been shown to inhibit fatty acid synthase, reducing IGF-1-induced activation of STAT3 in several melanoma cell lines.

Icaritin запасные части и сырье

Icaritin поставщик

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