| Company Name: |
ChemeGen |
| Tel: |
18818260767 |
| Email: |
2625930290@qq.com |
|
| | Betulonicacidmethylester Basic information |
| Product Name: | Betulonicacidmethylester | | Synonyms: | Betulonicacidmethylester;MethylBetulonate;1-isopropenyl-9-keto-5a,5b,8,8,11a-pentamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysene-3a-carboxylic acid methyl ester;methyl 5a,5b,8,8,11a-pentamethyl-9-oxo-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysene-3a-carboxylate;Lup-20(29)-en-28-oic acid, 3-oxo-, methyl ester | | CAS: | 4356-31-4 | | MF: | C31H48O3 | | MW: | 468.71 | | EINECS: | | | Product Categories: | | | Mol File: | 4356-31-4.mol |  |
| | Betulonicacidmethylester Chemical Properties |
| Melting point | 165 °C | | Boiling point | 521.3±33.0 °C(Predicted) | | density | 1.033±0.06 g/cm3(Predicted) | | solubility | DMF: 5 mg/ml | | form | A crystalline solid |
| | Betulonicacidmethylester Usage And Synthesis |
| Uses | Methyl betulonate (Betulonic acid methyl ester) is a triterpenoid. Methyl betulonate inhibits cell growth of eight tumor (including resistant) and two normal fibroblast cell lines with the IC50s >50.0 μM[1]. | | References | [1] Borkova L, et al. Synthesis and Cytotoxic Activity of Triterpenoid Thiazoles Derived from Allobetulin, Methyl Betulonate, Methyl Oleanonate, and Oleanonic Acid. ChemMedChem. 2017;12(5):390-398. DOI:10.1002/cmdc.201600626 |
| | Betulonicacidmethylester Preparation Products And Raw materials |
|