baohuoside II

Product Name: baohuoside II
CAS No.: 55395-07-8
Chemical Name: baohuoside II
Synonyms: Icarisoside-A;baohuoside II;IKarisoside A (Icarisoside-A;4H-1-Benzopyran-4-one,3-[(6-deoxy-a-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-;4H-1-Benzopyran-4-one, 3-[(6-deoxy-α-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-;3-[(6-Deoxy-alpha-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one;5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one;5,7-Dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-en-1-yl)-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one
CBNumber: CB61365562
Molecular Formula: C26H28O10
Formula Weight: 500.49
MOL File: 55395-07-8.mol

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baohuoside II Property

Boiling point:: 782.1±60.0 °C(Predicted)
Density: 1.53
form: Solid
pka: 6.31±0.40(Predicted)
color: Light yellow to yellow

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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Biosynth Carbosynth

Product number: FB74420
Product name: Baohuoside II
Packaging: 1mg
Price: $86
Updated: 2021/12/16

Biosynth Carbosynth

Product number: FB74420
Product name: Baohuoside II
Packaging: 2mg
Price: $150
Updated: 2021/12/16

Biosynth Carbosynth

Product number: FB74420
Product name: Baohuoside II
Packaging: 5mg
Price: $300
Updated: 2021/12/16

Biosynth Carbosynth

Product number: FB74420
Product name: Baohuoside II
Packaging: 10mg
Price: $510
Updated: 2021/12/16

AK Scientific

Product number: 9109AF
Product name: BaohuosideII
Packaging: 10mg
Price: $738
Updated: 2021/12/16

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baohuoside II Chemical Properties,Usage,Production

Uses

IKarisoside A (Icarisoside-A) is a natural flavonol glycoside and has anti-inflammatory properties.

References

[1] Choi HJ, et al. Ikarisoside A inhibits inducible nitric oxide synthase in lipopolysaccharide-stimulated RAW 264.7 cells via p38 kinase and nuclear factor-kappaB signaling pathways. Eur J Pharmacol. 2008 Dec 28;601(1-3):171-8. DOI:10.1016/j.ejphar.2008.09.032
[2] Choi HJ, eta l. Inhibition of osteoclastogenic differentiation by Ikarisoside A in RAW 264.7 cells via JNK and NF-kappaB signaling pathways. Eur J Pharmacol. 2010 Jun 25;636(1-3):28-35. DOI:10.1016/j.ejphar.2010.03.023
[3] Li X, Toyohira Y, Horisita T, et al. Ikarisoside A inhibits acetylcholine-induced catecholamine secretion and synthesis by suppressing nicotinic acetylcholine receptor-ion channels in cultured bovine adrenal medullary cells. Naunyn Schmiedebergs Arch Pharmacol. 2015;388(12):1259-1269. DOI:10.1007/s00210-015-1161-y

baohuoside II Preparation Products And Raw materials

Raw materials

Preparation Products

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baohuoside II Suppliers

China 134 India 1 United Kingdom 1 United States 12 Global 148

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View Lastest Price from baohuoside II manufacturers

Shanghai Standard Technology Co., Ltd.

Product: Baohuoside II 55395-07-8
Price: US $0.00/mg
Min. Order: 5mg
Purity: ≥98%(HPLC)
Supply Ability: 10 g
Release date: 2020-03-30

55395-07-8, baohuoside IIRelated Search:

Bismuth hydroxide nitrate oxide, BiO5.1 Baohuoside V Epmedin C Epimedin A baohuoside VII 3-[(6-Deoxy-3-O-beta-D-glucopyranosyl-alpha-L-mannopyranosyl)oxy]-7-(beta-D-glucopyranosyloxy)-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one IKARISOSIDE F Sagittatosdie B Epmedin B baohuoside I

3-[(6-Deoxy-alpha-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one

baohuoside II

Icarisoside-A

IKarisoside A (Icarisoside-A

4H-1-Benzopyran-4-one,3-[(6-deoxy-a-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-

4H-1-Benzopyran-4-one, 3-[(6-deoxy-α-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

5,7-Dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-en-1-yl)-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

55395-07-8

C26H28O10