Achilles

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Structural formula
Structural formula of Achilles
General
Surname Achilles
other names
  • L -Betonicin
  • L -4-hydroxystachydrin
  • L -4-hydroxyproline betaine
  • (2 S , 4 R ) -4-Hydroxy-1,1-dimethylpyrrolidin-1-ium-2-carboxylate
Molecular formula C 7 H 13 NO 3
External identifiers / databases
CAS number 515-25-3
EC number 208-195-6
ECHA InfoCard 100.007.451
PubChem 375481
ChemSpider 333078
Wikidata Q340267
properties
Molar mass 159.18 g mol −1
Physical state

firmly

density

1.0765 g cm −3 (25 ° C)

Melting point

254-256 ° C

safety instructions
GHS hazard labeling
no classification available
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Achillein (also: L -4-Hydroxystachydrin , L -Betonicin ) is a plant component from the group of pyrrolidine alkaloids . The compound - in the form of its carboxylate - is one of the betaines . Chemically, Achillein is an N , N -dimethylated derivative of the proteinogenic amino acid L - hydroxyproline .

Achilles has anti-inflammatory properties.

Occurrence

Common meadow yarrow ( Achillea millefolium )

Achilles was first found in the medicinal ziest Stachys officinalis , also betonia ; this led to the name "Betonicin". It is also found in various species of the yarrow ( Achillea ) and in the beach bean Canavalia maritima .

Individual evidence

  1. ^ Carl L. Yaws: Thermophysical properties of chemicals and hydrocarbons. William Andrew, 2008, ISBN 978-0-8155-1596-8 , p. 233.
  2. a b Jiaju Zhou, Guirong Xie, Xinjian Yan: Encyclopedia of Traditional Chinese Medicines - Molecular Structures, Pharmacological Activities, Natural Sources and Applications. Volume 1: Isolated Compounds A-C. Springer, 2011, ISBN 978-3-642-16734-8 , p. 273.
  3. This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
  4. ^ E. Nuremberg, P. Surmann: Hager's handbook of pharmaceutical practice. Volume 2, 5th edition. Birkhäuser, 1991, p. 49.