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| | 2',4'-Dihydroxy-3',6'-dimethoxychalcone Basic information |
| Product Name: | 2',4'-Dihydroxy-3',6'-dimethoxychalcone | | Synonyms: | 1-(2,4-Dihydroxy-3,6-diMethoxyphenyl)-3-phenylprop-2-en-1-one;2',4'-DIHYDROXY-3',6'-DIMETHOXYC;2-Propen-1-one, 1-(2,4-dihydroxy-3,6-dimethoxyphenyl)-3-phenyl-, (2E)-;4'-Dihydroxy-3';6'-dimethoxychalcone;(2E)-1-(2,4-Dihydroxy-3,6-dimethoxyphenyl)-3-phenyl-2-propen-1-one | | CAS: | 129724-43-2 | | MF: | C17H16O5 | | MW: | 300.31 | | EINECS: | | | Product Categories: | | | Mol File: | 129724-43-2.mol |  |
| | 2',4'-Dihydroxy-3',6'-dimethoxychalcone Chemical Properties |
| | 2',4'-Dihydroxy-3',6'-dimethoxychalcone Usage And Synthesis |
| Uses | 2',4'-Dihydroxy-3',6'-dimethoxychalcone is a natural product that can be isolated from Polygonum Lapathifolium. 2',4'-Dihydroxy-3',6'-dimethoxychalcone inhibits the growth of CCRF-CEM leukaemia cells and CEM/ADR5000 cells, with IC50 values of 10.67 and 18.60 μM, respectively[1][2]. | | References | [1] Ahmed M, et al. Isoflavan-4-ol, dihydrochalcone and chalcone derivatives from Polygonum Lapathifolium. Phytochemistry, 1990, 29(6):2009-2011.
[2] Nkuété AH, et al. Anti-leukemia activity of semi-synthetic phenolic derivatives from Polygonum limbatum Meisn. Chem Cent J. 2015 Jun 24;9:40. DOI:10.1186/s13065-015-0115-2 |
| | 2',4'-Dihydroxy-3',6'-dimethoxychalcone Preparation Products And Raw materials |
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