Jump to content

Festuclavine

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by JCW-CleanerBot (talk | contribs) at 03:28, 16 November 2018 (task, replaced: Organic & biomolecular chemistry → Organic & Biomolecular Chemistry). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Festuclavine
Names
IUPAC name
(6aR,9R,10aR)-7,9-Dimethyl-6,6a,8,9,10,10a-hexahydro-4H-indolo[4,3-fg]quinoline (cf. agroclavine)
Identifiers
3D model (JSmol)
ChemSpider
  • 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/s1
    Key: VLMZMRDOMOGGFA-WDBKCZKBSA-N
  • C[C@@H]1C[C@@H]2c3cccc4c3c(c[nH]4)C[C@H]2N(C1)C
Properties
C16H20N2
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).

Festuclavine is an ergoline fungal isolate.[1]

See also

Notes

  1. ^ 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.


Stub icon

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Festuclavine&oldid=869056171"