Fumigaclavine A

In today's world, Fumigaclavine A has become a topic of interest to a wide spectrum of society. The relevance of Fumigaclavine A transcends borders and contexts, significantly impacting the way we live and relate. From its influence on politics, the economy, culture and technology, to its impact on people's daily lives, Fumigaclavine A occupies a prominent place on the public agenda. In this article, we will explore the various dimensions of Fumigaclavine A and its importance in the contemporary world, offering a comprehensive analysis that allows a deep understanding of its scope and relevance today.

Fumigaclavine A
Names
IUPAC name
quinoline-10-yl] acetate
Other names
(8α,9β)-6,8-Dimethylergolin-9-ol acetate
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
KEGG
UNII
  • InChI=1S/C18H22N2O2/c1-10-9-20(3)15-7-12-8-19-14-6-4-5-13(16(12)14)17(15)18(10)22-11(2)21/h4-6,8,10,15,17-19H,7,9H2,1-3H3/t10-,15-,17-,18+/m1/s1
    Key: GJSSYQDXZLZOLR-ONUGHKICSA-N
  • C1CN(2CC3=CNC4=CC=CC(=C34)C21OC(=O)C)C
Properties
C18H22N2O2
Molar mass 298.386 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).

Fumigaclavine A is an antibacterial ergoline alkaloid produced by endophytic Aspergillus.[1]

Both 8α and 8β diastereomers (epimers) were named fumigaclavine A in scientific literature.[2]

See also

References

  1. ^ Pinheiro, EA; Carvalho, JM; Dos Santos, DC; Feitosa, AD; Marinho, PS; Guilhon, GM; De Souza, AD; Da Silva, FM; Marinho, AM (2012). "Antibacterial activity of alkaloids produced by endophytic fungus Aspergillus sp. EJC08 isolated from medical plant Bauhinia guianensis". Natural Product Research. 27 (18): 1633–8. doi:10.1080/14786419.2012.750316. PMID 23234304. S2CID 38933742.
  2. ^ Wallwey, Christiane; Li, Shu-Ming (2011-03-01). "Ergot alkaloids: structure diversity, biosynthetic gene clusters and functional proof of biosynthetic genes". Natural Product Reports. 28 (3): 496–510. doi:10.1039/C0NP00060D. ISSN 1460-4752. PMID 21186384.


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