Marmesin

Marmesin
Names
	IUPAC name (2S)-2-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one
	Other names Nodakenetin
Identifiers
CAS Number	13849-08-6;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL442813;
ChemSpider	296611;
PubChem CID	334704;
	InChI InChI=1S/C14H14O4/c1-14(2, 16)12-6-9-5-8-3-4-13(15)18-10(8)7-11(9)17-12/h3-5,7,12,16H,6H2, 1-2H3/t12-/m0/s1 Key: FWYSBEAFFPBAQU-LBPRGKRZSA-N;
	SMILES CC(C)([C@@H]1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O;
Properties
Chemical formula	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.

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.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.