Marmesin

Marmesin
Names
	Preferred IUPAC name (2S)-2-(2-Hydroxypropan-2-yl)-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one
	Other names Nodakenetin
Identifiers
CAS Number	13849-08-6 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL442813;
ChemSpider	296611;
PubChem CID	334704;
UNII	H5D33D6K5D ;
CompTox Dashboard (EPA)	DTXSID001030448 ;
	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	246.262 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]

Marmesin plays a central role in the biosynthesis of furocoumarins in the plant ruta graveolens, more commonly known as rue. It acts as the natural intermediate in the formation of the furan ring that leads to a 4’,5’-dihydro furocoumarin-derivative. This substance can then be transformed into psoralen and other furocoumarins present in rue. Upon feeding the herb a dose of marmesin, radioactivity became strongly incorporated into psoralen and thus the plant itself.^[2]

Spectra

IR Spectra

IR (ATR): νmax 3480, 2971, 1699, 1631, 1488 cm-1.^[3]

Proton-NMR

1H-NMR (300 MHz, CDCl3): δ 7.59 (d, J = 9.5 Hz, 1H, aromatic), 7.22 (s, 1H, aromatic), 6.75 (d, J = 21.6 Hz, 1H, aromatic), 6.20 (d, J = 9.5 Hz, 1H, aromatic), 4.74 (t, J = 8.8 Hz, 1H, CH), 3.28-3.15 (m, 2H, CH2), 1.87 (s, 1H, OH), 1.37 (s, 3H, CH3), 1.24 (s, 3H, CH3) ppm.^[4]

UV-Vis

UV: [neutral]λmax 217 (ε7420); 338 (ε17700)( MeOH) [neutral]λmax 332( EtOH).^[5]

Production

Synthesis of marmesin has been successfully conducted in the laboratory on multiple occasions. One way of doing so is by a strategy based on the palladium-catalyzed intramolecular coupling reaction. This reaction would construct the dihydropyran ring and synthesize the compound from the intermediate (-)-peucedanol. The key step in the overall synthesis uses catalytic asymmetric epoxidation of an enone.^[6]

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. PMID 5134594.
^ Caporale, G.; Dall’Acqua, F.; Capozzi, A.; Marciani, S.; Crocco, R. Studies on the biosynthesis of some furocoumarins present in Ruta graveolens. Zeitschrift für Naturforschung B 1971, 26, 1256-1259.
^ Ando, T.; Nagumo, M.; Ninomiya, M.; Tanaka, K.; Linhardt, R. J.; Koketsu, M. Synthesis of coumarin derivatives and their cytoprotective effects on t-BHP-induced oxidative damage in HepG2 cells. Bioorg. Med. Chem. Lett. 2018, 28, 2422-2425.
^ Kommera, R.; Bhimapaka, C. R. A simple and efficient approach for the preparation of dihydroxanthyletin, xanthyletin, decursinol and marmesin. Synthetic Communications 2020, 50, 3204-3211.
^ Anonymous Dictionary of natural products; Chapman & Hall: London, 1994.
^ Nemoto, T.; Ohshima, T.; Shibasaki, M. Enantioselective total syntheses of novel PKC activator (+)-decursin and its derivatives using catalytic asymmetric epoxidation of an enone. Tetrahedron Lett. 2000, 41, 9569-9574.

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.

[SteckBrown1971-1] 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. PMID 5134594.

[2] Caporale, G.; Dall’Acqua, F.; Capozzi, A.; Marciani, S.; Crocco, R. Studies on the biosynthesis of some furocoumarins present in Ruta graveolens. Zeitschrift für Naturforschung B 1971, 26, 1256-1259.

[3] Ando, T.; Nagumo, M.; Ninomiya, M.; Tanaka, K.; Linhardt, R. J.; Koketsu, M. Synthesis of coumarin derivatives and their cytoprotective effects on t-BHP-induced oxidative damage in HepG2 cells. Bioorg. Med. Chem. Lett. 2018, 28, 2422-2425.

[4] Kommera, R.; Bhimapaka, C. R. A simple and efficient approach for the preparation of dihydroxanthyletin, xanthyletin, decursinol and marmesin. Synthetic Communications 2020, 50, 3204-3211.

[5] Anonymous Dictionary of natural products; Chapman & Hall: London, 1994.

[6] Nemoto, T.; Ohshima, T.; Shibasaki, M. Enantioselective total syntheses of novel PKC activator (+)-decursin and its derivatives using catalytic asymmetric epoxidation of an enone. Tetrahedron Lett. 2000, 41, 9569-9574.

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