^Wallwey, C; Matuschek, M; Xie, XL; Li, SM (2010). "Ergot alkaloid biosynthesis in Aspergillus fumigatus: Conversion of chanoclavine-I aldehyde to festuclavine by the festuclavine synthase FgaFS in the presence of the old yellow enzyme FgaOx3". Organic & Biomolecular Chemistry. 8 (15): 3500–8. doi:10.1039/c003823g. PMID 20526482.
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festuclavine, ergoline, fungal, isolate, names, iupac, name, dimethylergoline, systematic, iupac, name, 10ar, dimethyl, octahydroindolo, quinoline, identifiers, number, model, jsmol, interactive, image, chemspider, 294963, pubchem, 332915, unii, gls7y869av, co. Festuclavine is an ergoline fungal isolate 1 Festuclavine Names IUPAC name 6 8b Dimethylergoline Systematic IUPAC name 6aR 9R 10aR 7 9 Dimethyl 4 6 6a 7 8 9 10 10a octahydroindolo 4 3 fg quinoline Identifiers CAS Number 436 41 9 Y 3D model JSmol Interactive image ChemSpider 294963 PubChem CID 332915 UNII GLS7Y869AV Y CompTox Dashboard EPA DTXSID00205432 InChI InChI 1S C16H20N2 c1 10 6 13 12 4 3 5 14 16 12 11 8 17 14 7 15 13 18 2 9 10 h3 5 8 10 13 15 17H 6 7 9H2 1 2H3 t10 13 15 m1 s1Key VLMZMRDOMOGGFA WDBKCZKBSA N SMILES C C H 1C C H 2c3cccc4c3c c nH 4 C C H 2N C1 C Properties Chemical formula C 16H 20N 2 Molar mass 240 350 g mol 1 Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa Infobox referencesSee also editFestuclavine dehydrogenaseNotes edit Wallwey C Matuschek M Xie XL Li SM 2010 Ergot alkaloid biosynthesis in Aspergillus fumigatus Conversion of chanoclavine I aldehyde to festuclavine by the festuclavine synthase FgaFS in the presence of the old yellow enzyme FgaOx3 Organic amp Biomolecular Chemistry 8 15 3500 8 doi 10 1039 c003823g PMID 20526482 nbsp This article about an alkaloid is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Festuclavine amp oldid 1152635511, wikipedia, wiki, book, books, library,
