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α-Viniferin
🥰Excellent
Catalog No. TN1378Cas No. 62218-13-7
Alias ALPHA-VINIFERIN
α-Viniferin known as 2-arylbenzofuran flavonoids, that are inhibitors of prostaglandin H2 synthetase. α-Viniferin has anti-Alzheimer's disease, anti-tuberculosis, anti-tumor, anti-inflammation, anti-diabetes and other pharmacological activitie
α-Viniferin
🥰Excellent
Catalog No. TN1378Alias ALPHA-VINIFERINCas No. 62218-13-7
α-Viniferin known as 2-arylbenzofuran flavonoids, that are inhibitors of prostaglandin H2 synthetase. α-Viniferin has anti-Alzheimer's disease, anti-tuberculosis, anti-tumor, anti-inflammation, anti-diabetes and other pharmacological activitie
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Product Introduction
Bioactivity
Chemical Properties
| Description | α-Viniferin known as 2-arylbenzofuran flavonoids, that are inhibitors of prostaglandin H2 synthetase. α-Viniferin has anti-Alzheimer's disease, anti-tuberculosis, anti-tumor, anti-inflammation, anti-diabetes and other pharmacological activitie |
| Targets&IC50 | Mycobacterium tuberculosis:4.6 μM(MIC50), Macrophages and pneumocytes:2.3-4.6 μM(MIC50), CYP3A4:1.2μM, CYP2C19:0.93μM |
| In vitro | α-Viniferin at 3 - 10 muM dose-dependently inhibited IFN-gamma-induced production of NO, IFN-gamma-inducible protein-10 (IP-10), or the monokine induced by IFN-gamma (MIG) in RAW 264.7 cells and also that of NO in primary macrophages-derived from C57BL/6 mice. Furthermore, α-Viniferin diminished IFN-gamma-induced protein levels of inducible NO synthase (iNOS), attenuated mRNA levels of iNOS, IP-10, or MIG as well as inhibited promoter activity of the iNOS gene[1].α-viniferin is a bioactive phytochemical compound obtained from Carex humilis, which has the antitubercular activity. α-Viniferin was active against both drug-susceptible and -resistant strains of Mycobacterium tuberculosis at MIC50s of 4.6 μM in culture broth medium and MIC50s of 2.3-4.6 μM inside macrophages and pneumocytes[2]. α-Viniferin strongly inhibited 7 of the 9 P450 (CYP) isoforms (except CYP2A6 and CYP2E1) in human. α-viniferin strongly inhibited CYP2C19-mediated omeprazole 5-hydroxylation and CYP3A4-catalyzed midazolam 1-hydroxylation with IC50 values of 0.93 and 1.2 μM, respectively[3]. |
| In vivo | Oral bioavailability of α-viniferin in mice was 4.2 %.[4] |
| Alias | ALPHA-VINIFERIN |
| Molecular Weight | 678.68 |
| Formula | C42H30O9 |
| Cas No. | 62218-13-7 |
| Smiles | OC(C=C1)=CC=C1[C@@H](O2)[C@@H](C3=CC(O)=CC4=C3[C@@H](C5=CC(O)=CC(O6)=C75)[C@H](C8=CC=C(O)C=C8)O4)C9=C2C=C(O)C=C9[C@H]7[C@@H]6C%10=CC=C(O)C=C%10 |
| Relative Density. | 1.517 g/cm3 (Predicted) |
Storage & Solubility Information
| Storage | store at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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