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baohuoside I

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baohuoside I manufacturers

  • Baohuoside I
  • Baohuoside I pictures
  • $60.00
  • 2026-08-20
  • CAS:113558-15-9
  • Purity: 98.14%
  • Supply Ability: 10g
  • baohuoside I
  • baohuoside I pictures
  • 2026-05-22
  • CAS:113558-15-9
  • Min. Order: 1kg
  • Purity: 99.8%
  • Supply Ability: 1000 kg
baohuoside I Basic information
Product Name:baohuoside I
Synonyms:3-(α-L-Rhamnopyranosyloxy)-4'-methoxy-5,7-dihydroxy-8-prenylflavone;5,7-Dihydroxy-4'-methoxy-8-prenyl-3-(α-L-rhamnopyranosyloxy)flavone;Baohuoside-1;Icarisid II;BAOHUOSIDE I; ANHYDROICARITIN; ICARISIDE II;Baohuoside I(Icariside II);baohuoside I;3-[(6-Deoxy-alpha-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one
CAS:113558-15-9
MF:C27 H30 O10
MW:514.52
EINECS:246-914-5
Product Categories:phytochemical;pharmaceutical intermediate;chemical reagent;standardized herbal extract;reference standards from Chinese medicinal herbs (TCM).
Mol File:113558-15-9.mol
baohuoside I Structure
baohuoside I Chemical Properties
Melting point 202-203 °C
Boiling point 759.4±60.0 °C(Predicted)
density 1.46
storage temp. Inert atmosphere,Room Temperature
solubility DMSO, Methanol
pka6.29±0.40(Predicted)
form Solid
color Light Yellow
Optical Rotation[α]/D -101 to -129°, c =0.5 in ethanol
Cosmetics Ingredients FunctionsSKIN PROTECTING
BLEACHING
SKIN CONDITIONING
SKIN CONDITIONING - EMOLLIENT
ANTIOXIDANT
InChIKeyNGMYNFJANBHLKA-MNYOFVDPNA-N
SMILESC(C1C(=CC(O)=C2C(C(O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)=C(C3C=CC(OC)=CC=3)OC=12)=O)O)C=C(C)C |&1:10,12,14,16,18,r|
Safety Information
WGK Germany WGK 3
HS Code 29329990
Storage Class11 - Combustible Solids
MSDS Information
baohuoside I Usage And Synthesis
Chemical PropertiesYellow needle-shaped crystals, soluble in methanol, derived from the whole herb of Epimedium.
UsesBaohuoside I is an inhibitor of cell growth and also is a down-regulator of durvivin and cyclin D1 expression. Used in the treatment of esophageal cancer. Anti-cancer agent.
DefinitionChEBI: A glycosyloxyflavone that is 3,5,7-trihydroxy-4'-methoxy-8-prenylflavone in which the hydroxy group at position 3 has been converted to its alpha-L-rhamnopyranoside.
Biological ActivityIcariside II (Baohuoside-I) is a flavonoid with cytoprotective, neuroprotective, antiproliferative, and erectile function properties.
Synthesis
Icariin

489-32-7

baohuoside I

113558-15-9

The general procedure for the synthesis of 5,7-dihydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-buten-1-yl)-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-4H-benzopyran-4-one from Icariin was performed as follows: firstly, mycelia from agar slants ( 2 cm2) of C. blakesleeana mycelium was transferred to 100 mL of medium and incubated at 30 °C and 175 rpm for 36 h to prepare the inoculum. Subsequently, 10 mL of inoculum was added to 1000 mL of liquid medium and the flasks were placed on a rotary shaker and pre-cultured for 36 h at 175 rpm, 30°C. After completion of the pre-culture, 100 mg of Icariin was dissolved in 2 mL of methanol and added to 2 L of medium for preparative biotransformation to reach a final concentration of 50 mg/L. After continuing the culture for 5 days, the culture was filtered, and the filtrate was extracted five times with equal volumes of EtOAc. At the same time, suspension cells of C. blakesleeana (5.2 g) were extracted using 1000 mL EtOAc. All EtOAc extracts were combined and concentrated under reduced pressure. The resulting residue (1.6 g) was upsampled onto an ODS column (200 g, 10 cm × 50 cm) and eluted with MeOH-HO (10% to 90% gradient, flow rate 2.0 mL/min). Finally, 90.1 mg of icariside II was obtained from the 60% MeOH-eluted grade (500 mL) with a purity of 96.5%.

References[1] Journal of Molecular Catalysis B: Enzymatic, 2015, vol. 122, p. 141 - 146
[2] Patent: CN104530127, 2016, B. Location in patent: Paragraph 0156-0159
[3] Patent: CN104387430, 2017, B. Location in patent: Paragraph 0109; 0110; 0111; 0112
[4] Journal of Natural Products, 2008, vol. 71, # 9, p. 1513 - 1517
[5] Journal of Asian Natural Products Research, 2015, vol. 17, # 6, p. 656 - 661
baohuoside I Preparation Products And Raw materials
Raw materialsIcariin-->Methanol
Preparation ProductsIcaritin
Tag:baohuoside I(113558-15-9) Related Product Information
Epmedin B PULCHINENOSIDE B4 1-[2-Hydroxy-4-methoxy-5-(3-methyl-2-butenyl)phenyl]-3-(4-hydroxyphenyl)-2-propen-1-one hydroxysafflor yellow A Epmedin C AURANTIO-OBTUSIN daurisoline Periplocoside Bakuchiol ATRACTYLON Psoralen HINOKIFLAVONE Epimedin A Musk ketone Glabridin Wogonin Kaempferol Icariin