Cardamomin
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| Names | |
|---|---|
| IUPAC name
(E)-1-(2,4-dihydroxy-6-methoxyphenyl)-3-phenylprop-2-en-1-one | |
| Other names
(2E)-1-(2,4-Dihydroxy-6-methoxyphenyl)-3-phenyl-2-propen-1-one | |
| Identifiers | |
19309-14-9  = | |
| ChEMBL | ChEMBL378104  |
| ChemSpider | 557026 |
| |
| Jmol-3D images | Image |
| PubChem | 641785 |
| |
| UNII | H8KP1OJ8JX |
| Properties | |
| C16H14O4 | |
| Molar mass | 270.27 g/mol |
| Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
| verify (what is: /?) | |
| Infobox references | |
Cardamomin (also known as cardamonin) is a chalconoid that has been isolated from several plants including Alpinia katsumadai[1] and Alpinia conchigera.[2] It has received growing attention from the scientific community due to the expectations toward its benefits to human health.[3]
References
- ↑ Kimura, Y.; Takahashi, S.; Yoshida, I. (1968). "Studies on the constituents of Alpinia. XII. On the constituents of the seeds of Alpinia katsumadai hayata. I. The structure of cardamomin". Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 88 (2): 239–241. PMID 5692492.
- ↑ Lee, J. -H.; Jung, H. S.; Giang, P. M.; Jin, X.; Lee, S.; Son, P. T.; Lee, D.; Hong, Y. S.; Lee, K.; Lee, J. J. (2005). "Blockade of Nuclear Factor- B Signaling Pathway and Anti-Inflammatory Activity of Cardamomin, a Chalcone Analog from Alpinia conchigera". Journal of Pharmacology and Experimental Therapeutics 316 (1): 271–278. doi:10.1124/jpet.105.092486. PMID 16183703.
- ↑ Gonçalves, Luís Moreira (2014). "An Overview on Cardamonin". Journal of Medicinal Food 17 (6): 633–640. doi:10.1089/jmf.2013.0061.
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