-
(±)-γ-Tocopherol
- names:
3,4-dihydro-2,7,8-trimethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-ol
- CAS號:
7616-22-0
MDL Number: - MF(分子式): C28H48O2 MW(分子量): 416.69
- EINECS: Reaxys Number:
- Pubchem ID: Brand:BIOFOUNT
| 貨品編碼 | 規(guī)格 | 純度 | 價格 (¥) | 現(xiàn)價(¥) | 特價(¥) | 庫存描述 | 數(shù)量 | 總計 (¥) |
|---|
| 中文別名 | 3,4-dihydro-2,7,8-trimethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-ol |
| 英文別名 | (±)-γ-Tocopherol, 7,8-Dimethyltocol, all-rac-γ-Tocopherol, DL-γ-Tocopherol |
| CAS號 | 7616-22-0 |
| Inchi | InChI=1S/C28H48O2/c1-20(2)11-8-12-21(3)13-9-14-22(4)15-10-17-28(7)18-16-25-19-26(29)23(5)24(6)27(25)30-28/h19-22,29H,8-18H2,1-7H3 |
| InchiKey | QUEDXNHFTDJVIY-UHFFFAOYSA-N |
| 分子式 Formula | C28H48O2 |
| 分子量 Molecular Weight | 416.69 |
| 溶解度Solubility | |
| 性狀 | A solution in hexane |
| 儲藏條件 Storage conditions | Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years). |
| 產(chǎn)品說明 | (±)-γ-Tocopherol(CAS:7616-22-0):僅限應(yīng)用于工業(yè)或者科學(xué)研究過程中非醫(yī)療目的,不應(yīng)用于人類或動物的臨床診斷以及治過程療,該產(chǎn)品非藥用,非食用。 |
| Introduction | (±)-γ-Tocopherol is a form of vitamin E with antioxidant and anti-inflammatory properties. It traps and detoxifies reactive nitrogen oxide species, including nitrogen dioxide, in cell-free assays. It also reduces the synthesis of prostaglandin E2 (PGE2) induced by LPS in RAW 264.7 macrophages and by IL-1β in A549 cells. (±)-γ-Tocopherol inhibits LPS-induced nitrite release and inducible nitric oxide synthase (iNOS) expression in RAW 264.7 cells and reduces COX-2 activity in A549 cells pretreated with IL-1β. Serum levels of (±)-γ-tocopherol are decreased in patients with cardiovascular disease. |
| Application1 | |
| Application2 | |
| Application3 |
| [1]Jiang, Q., Christen, S., Shigenaga, M.K., et al. γ-Tocopherol, the major form of vitamin E in the US diet, deserves more attention. American Journal of Clinical Nutrition 74, 714-722 (2001).2. Cooney, R.V., Franke, A.A., Harwood, P.J., et al. γ-Tocopherol detoxification of nitrogen dioxide: Superiority to α-tocopherol. Proceedings of the National Academy of Sciences of the United States of America 90, 1771-1775 (1993).3. Jiang, Q., Elson-Schwab, I., Courtemanche, C., et al. γ-Tocopherol and its major metabolite, in contrast to α-tocopherol, inhibit cyclooxygenase activity in macrophages and epithelial cells. Proceedings of the National Academy of Sciences of the United States of America 97, 11494-11499 (2000). |
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