- Vicenin 2
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- $79.00 / 1mg
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2026-02-02
- CAS:23666-13-9
- Min. Order:
- Purity: 99.99%
- Supply Ability: 10g
- Vicenin-2
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- $0.00 / 20mg
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2023-02-24
- CAS:23666-13-9
- Min. Order: 20mg
- Purity: ≥98%(HPLC)
- Supply Ability: 10 g
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| | VICENIN Basic information |
| Product Name: | VICENIN | | Synonyms: | 2-(4-Hydroxyphenyl)-5,7-dihydroxy-6,8-bis(β-D-glucopyranosyl)-4H-1-benzopyran-4-one;6,8-Di(β-D-glucopyranosyl)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one;Apigenin 6,8-C-diglucoside;5,7-Dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one;Vicenin-2;Vicenin-II;4H-1-Benzopyran-4-one,6,8-di-b-D-glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-;6,8-Di-C-β-D-glucopyranosylapigenin | | CAS: | 23666-13-9 | | MF: | C27H30O15 | | MW: | 594.52 | | EINECS: | | | Product Categories: | | | Mol File: | 23666-13-9.mol |  |
| | VICENIN Chemical Properties |
| Melting point | >250 °C (decomp) | | Boiling point | 974.7±65.0 °C(Predicted) | | density | 1.758±0.06 g/cm3(Predicted) | | storage temp. | Hygroscopic, -20°C Freezer, Under inert atmosphere | | solubility | Methanol (Slightly, Heated, Sonicated), DMSO (Slightly) | | pka | 5.68±0.40(Predicted) | | form | Solid | | color | Light Yellow to Yellow | | Water Solubility | sparingly soluble in water | | Stability: | Hygroscopic | | InChIKey | FIAAVMJLAGNUKW-YFDIWHCFNA-N | | SMILES | OC[C@H]1O[C@@H](C2=C(O)C([C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C4C(C(C=C(C5=CC=C(O)C=C5)O4)=O)=C2O)[C@H](O)[C@@H](O)[C@@H]1O |
| WGK Germany | 3 | | Storage Class | 11 - Combustible Solids |
| | VICENIN Usage And Synthesis |
| Chemical Properties | White crystalline powder, soluble in organic solvents such as methanol, ethanol, and DMSO, derived from Desmodium sibiricum. | | Uses | Vicenin 2 (CAS# 23666-13-9) is a biologically active compound extracted from Hypericum salsugineum and displays significant anti-cancer effects on breast carcinoma cell lines. | | Definition | ChEBI: Isovitexin 8-C-beta-glucoside is a C-glycosyl compound that is isovitexin in which the hydrogen at position 8 is replaced by a beta-D-glucosyl residue. It has a role as a metabolite. It is a trihydroxyflavone and a C-glycosyl compound. It is functionally related to an isovitexin. | | Synthesis | A method for simultaneous isolation of schaftoside, vicenin-2, and ecdysterone from Sagina japonica:
1. Ethanol extraction, followed by solvent partitioning to obtain an n-butanol extract.
2. The extract is fractionated on an AB-8 macroporous resin column, eluting with 50% ethanol to enrich the target compounds.
3. The enriched fraction is separated on an ODS reversed-phase column, yielding three preliminary fractions.
4. Impure vicenin-2 and schaftoside are further purified separately on silica gel columns. | | in vivo | Vicenin 2 (50 mg/kg; orally administration; for 7 days) effectively reduces the MPO activity, attenuates the expression of pro-inflammatory cytokines and key inflammatory markers, in DSS-induced colitis mice[3]. | Animal Model: | Male C57BL/6J mice (25 g) treated with Dextran sulfate sodium (DSS)[3] | | Dosage: | 50 mg/kg | | Administration: | Orally administration; for 7 days | | Result: | Effectively suppressed DSS-induced colitis by attenuating expressions of key inflammatory mediators. |
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| | VICENIN Preparation Products And Raw materials |
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