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| HOMOORIENTIN Basic information |
Product Name: | HOMOORIENTIN | Synonyms: | 2-(3,4-Dihydroxyphenyl)-6-β-D-glucopyranosyl-5,7-dihydroxy-4H-1-benzopyran-4-one;6-(β-D-Glucopyranosyl)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one;Isoorientin/HoMoorientin;lespecapittoside;2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one;2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-methylol-tetrahydropyran-2-yl]chromone;HoMoorientin, froM PolygonuM orientale;IsoorientinI | CAS: | 4261-42-1 | MF: | C21H20O11 | MW: | 448.38 | EINECS: | | Product Categories: | Tetra-substituted Flavones;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract | Mol File: | 4261-42-1.mol | |
| HOMOORIENTIN Chemical Properties |
Melting point | 245-246°C | Boiling point | 856.7±65.0 °C(Predicted) | density | 1.759±0.06 g/cm3(Predicted) | storage temp. | 2-8°C | solubility | methanol: soluble5mg/mL, clear, colorless to yellow | form | powder | pka | 5.90±0.40(Predicted) | color | yellow | Stability: | Hygroscopic | InChIKey | ODBRNZZJSYPIDI-VJXVFPJBSA-N | LogP | 1.580 (est) |
Safety Statements | 24/25 | WGK Germany | 3 | HS Code | 29389090 |
| HOMOORIENTIN Usage And Synthesis |
Chemical Properties | Pale Yellow Solid | Uses | Isoorientin is a flavonoid compound that can be isolated from the passion flower, and several other species of plants. Isoorientin has also shown to exert antioxidant, anti-nociceptive, anti-inflammat
ory and gastroprotective activities in several studies. | Uses | Reference Standard in the analysis of herbal medicinal products | Definition | ChEBI: A flavone C-glycoside consisting of luteolin having a beta-D-glucosyl residue at the 6-position. | General Description | Produced and qualified by HWI pharma services GmbH. Exact content by quantitative NMR can be found on the certificate. | Biochem/physiol Actions | C-glycosyl flavone with anti-inflammatory, antimicrobial and antioxidant properties. Induces antioxidant response through PI3K singaling. |
| HOMOORIENTIN Preparation Products And Raw materials |
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