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Icaritin

Icaritin Suppliers list
Company Name: Shaanxi Cuikang Pharmaceutical Technology Co., Ltd
Tel: +8618829768577
Email: gao490372054@gamil.com
Products Intro: Product Name:Icaritin
CAS:118525-40-9
Purity:0.95;0.97;0.98;0.99 Package:mg;g;kg;t
Company Name: PNP Biotech Co. Ltd
Tel: +8618516098983
Email: sales@pnpbiotech.com
Products Intro: Product Name:Icaritin
CAS:118525-40-9
Purity:Inquiry Package:25kg;0.00;USD
Company Name: Shaanxi Cuikang Pharmaceutical Technology Co., Ltd
Tel: +86-19164747840 +86-13119157289
Email: 13119157289@163.com
Products Intro: Product Name:Icaritin
CAS:118525-40-9
Purity:>=0.98 Package:G/bottle; Kg/bag; 25kg/barrel Remarks:Purity: 98%+ | in stock
Company Name: Shaanxi Haibo Biotechnology Co., Ltd
Tel: +undefined18602966907
Email: qinhe02@xaltbio.com
Products Intro: Product Name:Icaritin
CAS:118525-40-9
Purity:99% Package:25kg Remarks:White Powder
Company Name: Chongqing Zhihe Biopharmaceutical Co., Ltd.
Tel: +86-18580541567 +86-17782035140
Email: sales@zhswyy.com
Products Intro: Product Name:Icaritin
CAS:118525-40-9
Purity:>=98% Package:1kg;|5kg;|25kg

Icaritin manufacturers

  • Icaritin
  • Icaritin pictures
  • $0.00 / 1kg
  • 2024-04-24
  • CAS:118525-40-9
  • Min. Order: 0.10000000149011612kg
  • Purity: ≥98%
  • Supply Ability: 20tons
  • Icaritin
  • Icaritin pictures
  • $1.00 / 1kg
  • 2024-04-15
  • CAS:118525-40-9
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 5ton/month
  • Icaritin
  • Icaritin pictures
  • $0.00 / 25kg
  • 2024-04-12
  • CAS:118525-40-9
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 2000ton
Icaritin Basic information
Product Name:Icaritin
Synonyms:ICARITIN;3,5,7-Trihydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one;3,7-bis(2-hydroxyethyl)icaritin;Icaritin, >98%;3,5,7-trihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one;Icaritin(Anhydroicaritin);Icaritin>;4H-1-Benzopyran-4-one,3,5,7-trihydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-buten-1-yl)-
CAS:118525-40-9
MF:C21H20O6
MW:368.38
EINECS:
Product Categories:plant extract;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals
Mol File:118525-40-9.mol
Icaritin Structure
Icaritin Chemical Properties
Melting point 239℃
Boiling point 582.0±50.0 °C(Predicted)
density 1.359
Fp 206.7℃
storage temp. 2-8°C
solubility DMSO: soluble5mg/mL, clear (warmed)
form powder
pka6.44±0.40(Predicted)
color light yellow to dark yellow
λmax368nm(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
Safety Information
WGK Germany 3
RTECS DJ3100870
HS Code 29329990
MSDS Information
Icaritin Usage And Synthesis
Chemical PropertiesYellow crystalline powder, soluble in methanol, ethanol, DMSO and other organic solvents, derived from epimedium.
UsesIcaritin 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).
Biochem/physiol ActionsIcaritin is a component of Epimedium flavonoid isolated from Herba Epimedii, which enhances osteoblastic differentiation of mesenchymal stem cells (MSCs) while it inhibits adipogenic differentiation of MSCs by inhibiting PPAR-g pathway. Icaritin has no effect on MSCs proliferation. Also, icaritin potently inhibits chronic myeloid leukemia (CML) and breast cancer cells proliferation most likely by modulation of MAPK/ERK/JNK and JAK2/STAT3 /AKT signaling. As other flavonoids, icaritin may exert estrogen-like activities.
SynthesisThe 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
Mode of actionIcaritin 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 Preparation Products And Raw materials
Raw materialsIcaritin-->Icariin-->Icariside I-->baohuoside I-->KAEMPFEROLTETRAACETATE-->Dimethyl sulfate
Preparation ProductsDesmethylanhydroicaritin
Tag:Icaritin(118525-40-9) Related Product Information
Baohuoside V (+/-)-Naringenin Quercetin Epimedium Extract Shikonin Icariin epimedoside A 4H-1-Benzopyran-4-one, 3-[(6-deoxy-α-L-mannopyranosyl)oxy]-5,7-dihydroxy-8-(3-hydroxy-3-methylbutyl)-2-(4-methoxyphenyl)- Genipin Icariside I Peimine 13,14-Didehydromatridin-15-one Catalpol Cabazitaxel ASTRAGALIN Paclitaxel Anhydroicaritin Docetaxel