Artemisin

In this article, we will explore the importance of Artemisin in today's society. From its relevance in history to its impact on the modern world, Artemisin has been a topic of constant interest for academics, experts, and everyday people alike. Through a detailed and exhaustive analysis, we will examine the various facets of Artemisin and its influence on different aspects of society, culture and everyday life. Additionally, we will address the controversies and debates that have surrounded Artemisin, as well as its evolution over time. This article aims to provide a complete and balanced view of Artemisin, in order to deepen its understanding and appreciation in the current context.

Not to be confused with Artemisinin.
Artemisin
Names
Preferred IUPAC name
(3S,3aR,4S,5aS,9bS)-4-Hydroxy-3,5a,9-trimethyl-3a,5,5a,9b-tetrahydronaphthofuran-2,8(3H,4H)-dione
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
KEGG
UNII
  • Key: LUHMMHZLDLBAKX-DBIGVJDZSA-N
  • InChI=1S/C15H18O4/c1-7-9(16)4-5-15(3)6-10(17)11-8(2)14(18)19-13(11)12(7)15/h4-5,8,10-11,13,17H,6H2,1-3H3/t8-,10-,11+,13-,15+/m0/s1
  • C=1C(=O)C(C)=C2(C1)(C(1(C(O21)=O)C)O)C
Properties
C15H18O4
Molar mass 262.305 g·mol−1
Melting point 203 °C (397 °F; 476 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).

Artemisin is a sesquiterpene lactone, similar in structure to α-santonin.[1][2]

See also

References

  1. ^ SUMI, Masao (1956). "The Structure of Artemisin". Proceedings of the Japan Academy. 32 (9): 684–687. doi:10.2183/pjab1945.32.684.
  2. ^ ApSimon, John (2009). The Total Synthesis of Natural Products. John Wiley & Sons. ISBN 9780470129517.
  • Media related to Artemisin at Wikimedia Commons


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