- IKarisoside A
-
- $63.00
-
2026-07-15
- CAS:55395-07-8
- Purity: 99.83%
- Supply Ability: 10g
- Baohuoside II
-
-
2023-02-24
- CAS:55395-07-8
- Min. Order: 5mg
- Purity: ≥98%(HPLC)
- Supply Ability: 10 g
|
| | baohuoside II Basic information |
| Product Name: | baohuoside II | | Synonyms: | 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 | | CAS: | 55395-07-8 | | MF: | C26H28O10 | | MW: | 500.49 | | EINECS: | | | Product Categories: | | | Mol File: | 55395-07-8.mol |  |
| | baohuoside II Chemical Properties |
| Boiling point | 782.1±60.0 °C(Predicted) | | density | 1.53 | | form | Solid | | pka | 6.31±0.40(Predicted) | | color | Light yellow to yellow |
| | baohuoside II Usage And Synthesis |
| 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 |
|