(+)-marmesin
Sign in to saveAlso known as S-(+)-marmesin, (+)-2,3-dihydro-2-(1-hydroxy-1-methylethyl)-7H-furo[3,2-g][1]benzopyran-7-one, (S)-(+)-2,3-dihydro-2-(1-hydroxy-1-methylethyl)-7H-furo[3,2-g][1]benzopyran-7-one, (S)-2,3-dihydro-2-(1-hydroxy-1-methylethyl)-7H-furo[3,2-g][1]benzopyran-7-one, (S)-marmesin
Marmesin (nodakenetin) is a chemical compound precursor in psoralen and linear furanocoumarins biosynthesis.
Wikidata facts
- Subclass of
- furanocoumarin
- Mass
- 246.089
Show 5 more facts
- found in taxon
- Rutaceae
- chemical formula
- C₁₄H₁₄O₄
- canonical SMILES
- CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O
- isomeric SMILES
- CC(C)([C@@H]1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O
- Commons category
- Marmesin
Sources (2)
via Wikidata · CC0
~2 min read
Encyclopedic overview
7 sectionsContents
- Spectra
- IR Spectra
- Proton-NMR
- UV-Vis
- Production
- References
- External links
Marmesin (nodakenetin) is a chemical compound precursor in psoralen and linear furanocoumarins biosynthesis.
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. It is constituent of Aegle marmelos, Ammi majus, Poncirus trifoliata and Prangos bucharica and others
Excerpted from Wikipedia’s “(+)-marmesin” article, available under the CC BY-SA 4.0 licence.