Marmesin
Names | |
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IUPAC name
(2S)-2-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one | |
Other names
Nodakenetin | |
Identifiers | |
13849-08-6 | |
3D model (Jmol) | Interactive image |
ChEMBL | ChEMBL442813 |
ChemSpider | 296611 |
PubChem | 334704 |
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Properties | |
C14H14O4 | |
Molar mass | 246.26 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Marmesin (nodakenetin) is a chemical compound precursor in psoralen and linear furanocoumarins biosynthesis.[1]
References
- ↑ Steck, Warren; Brown, Stewart A. (1971). "Comparison of (+)- and (−)-Marmesin as Intermediates in the Biosynthesis of Linear Furanoconmarins". Biochemistry and Cell Biology. 49 (11): 1213–1216. doi:10.1139/o71-174. ISSN 1208-6002.
External links
- Abu-Mustafa, Effat A.; Fayez, M. B. E. (1961). "Natural Coumarins. I. Marmesin and Marmesinin, Further Products from the Fruits of Ammi majus L.". The Journal of Organic Chemistry. 26 (1): 161–166. doi:10.1021/jo01060a039. ISSN 0022-3263.
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