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| licarin B Basic information |
Product Name: | licarin B | Synonyms: | 1,3-Benzodioxole,5-[(2R,3R)-2,3-dihydro-7-Methoxy-3-Methyl-5-(1E)-1-propenyl-2-benzofuranyl]-(9CI);licarin B;5-[(2S)-2,3-Dihydro-7-methoxy-3β-methyl-5-[(E)-1-propenyl]benzofuran-2-yl]-1,3-benzodioxole;5-((2R,3R)-2,3-Dihydro-7-methoxy-3-methyl-5-(1E)-1-propenyl-2-benzofuranyl)-1,3-benzodioxole;5-[(3S)-7-methoxy-3-methyl-5-[(E)-prop-1-enyl]-2,3-dihydro-1-benzofuran-2-yl]-1,3-benzodioxole;Licarine B;1,3-Benzodioxole, 5-[(2R,3R)-2,3-dihydro-7-methoxy-3-methyl-5-(1E)-1-propen-1-yl-2-benzofuranyl]-;(-)-Licarin B | CAS: | 51020-87-2 | MF: | C20H20O4 | MW: | 324.37 | EINECS: | 2017-001-1 | Product Categories: | chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;reagent;standard substance | Mol File: | 51020-87-2.mol | |
| licarin B Chemical Properties |
Boiling point | 428.5±45.0 °C(Predicted) | density | 1.201±0.06 g/cm3(Predicted) | storage temp. | 2-8°C | solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | form | powder | color | White |
| licarin B Usage And Synthesis |
Chemical Properties | White crystals, soluble in methanol, ethanol, DMSO and other organic solvents, derived from nutmeg, Lauraceae (Lauraceae) Licarin aritu Ducke trunk (yield: 0.35%) Machilus japonica Sieb.et Zucc. Ye Hongnan Machilus thunbergii Sieb.et Zucc. Bark, wood, leaves. | Uses | Licarin B has antibacterial, anti-inflammatory, sedative and anti-tumor effects. | Biological Activity | Licarin B, derived from the seeds of Myristica fragrans, is an inhibitor of NO production and improves insulin sensitivity by activating PPARγ and GLUT4 in the IRS-1/PI3K/AKT pathway. | in vitro | Licarin B (5 μM, 10 μM, 15 μM. 8 days) moderately increases TG accumulation during adipogenic differentiation and showed partial PPARg agonist activity in 3T3-L1 preadipocytes. Cell Viability Assay < /p> Cell Line: | 3T3-L1 cell. | Concentration: | 1-500 μM. | Incubation Time: | 48 h. | Result: | Did not cause significant cell death up to 500 μM concentration. | Cell Viability Assay Cell Line: | 3T3-L1 cell. | Concentration: | 5 μM, 10 μM, 15 μM. | Incubation Time: | 8 days (replaced every 2 days). | 8 days (replaced every 2 days). | td> Result: | LB at 15 μM concentration significantly promoted adipocyte differentiation and caused intracellular TG accumulation. | < span class="view_more"> | target | PPAR | GLUT | PI3K | Akt | IRS-1 |
| licarin B Preparation Products And Raw materials |
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