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| | DEACETYLNOMILIN Basic information |
| Product Name: | DEACETYLNOMILIN | | Synonyms: | 1-Hydroxy-1,2-dihydroobacunoic acid 3,4-lactone;1-Hydroxy-1,2-dihydroobacunoic acid ε-lactone;Desacetylnomilin;Oxireno[4,4a]-2-benzopyrano[6,5-g][2]benzoxepin-3,5,9(3aH,4bH,6H)-trione, 1-(3-furanyl)decahydro-11-hydroxy-4b,7,7,11a,13a-pentamethyl-, (1S,3aS,4aR,4bR,6aR,11S,11aR,11bR,13aS)- | | CAS: | 3264-90-2 | | MF: | C26H32O8 | | MW: | 472.53 | | EINECS: | | | Product Categories: | Coumarins | | Mol File: | 3264-90-2.mol |  |
| | DEACETYLNOMILIN Chemical Properties |
| Melting point | 253-255 °C (decomp) | | Boiling point | 659.1±55.0 °C(Predicted) | | density | 1.35±0.1 g/cm3(Predicted) | | pka | 13.50±0.70(Predicted) |
| | DEACETYLNOMILIN Usage And Synthesis |
| Uses | Deacetylnomilin can be isolated from Citrus reticulata and has antibacterial and antifungal activity. Deacetylnomilin is a potent inhibitor of cell proliferation with an IC50 value of 0.005 ug/mL against estrogen receptor-positive (ER+) cells[1][2]. | | References | [1] Guthri N, et al. Inhibition of human breast cancer cells by citrus limonoids[M]. 2000.
[2] Khalil AT, et al. Limonoids from Citrus reticulata. Z Naturforsch C J Biosci. 2003 Mar-Apr;58(3-4):165-70. DOI:10.1515/znc-2003-3-403 |
| | DEACETYLNOMILIN Preparation Products And Raw materials |
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