Chemistry:Quinolizidine alkaloids
Quinolizidine alkaloids are natural products that have a quinolizidine structure; this includes the lupine alkaloids.[1][2][3]
Occurrence
Quinolizidine alkaloids can be found in the plant family of legumes, especially in papilionaceous plants. While the lupine alkaloids (following their name) can be found in lupines, tinctorin, for example, was isolated from the dyer's broom.[4][1]
Examples
More than 200 quinolizidine alkaloids are known which can be classified into 6 structural types:
- the lupinine type with 34 known structures, including lupinine and its derivatives
- the camoensine type with 6 known structures, including camoensin
- the spartein type with 66 structures, including sparteine, lupanine, angustifoline
- the α-pyridone type with 25 structures, including anagyrine and cytisine
- the matrine type with 31 structures, including matrine
- and the ormosanin type with 19 structures, including ormosanine.[2]
-Lupinine_Structural_Formula_V2.svg)
-(-)-Sparteine_Structural_Formula_V2.svg)
-(-)-Lupanine_Structural_Formula_V2.svg)
-Anagyrine_Structural_Formula_V1.svg)
-Matrine_Structural_Formula_V2.svg)
Properties
Cytisine is the toxic main alkaloid of laburnum. Similar to nicotine, it has a stimulating to hallucinogenic effect in low doses and a respiratory paralysing effect in higher doses. Cytisine and matrine are active ingredients of the Sophora beans from Mexico and the cow Seng and Shinkyogan drugs from China and Japan.[1]
Quinolizidine alkaloids defend plants against pests and diseases and breeding to reduce QA concentrations lowers these resistances.[5] They have various effects on warm-blooded animals and lead to poisoning of grazing livestock (sheep and cattle). Cytisin and anagyrin are particularly responsible for this. The effects of poisoning are stimulation, coordination disorders , shortness of breath, cramps and finally death from respiratory paralysis. Anagyrin acts teratogenic. The only quinolizidine alkaloid used therapeutically is sparteine,[2] which has an antiarrhythmic and labor-promoting effect.[1]
References
- ↑ 1.0 1.1 1.2 1.3 E. Breitmaier (1997) (in German), Alkaloide, Wiesbaden: Springer Fachmedien, pp. 45ff., ISBN 9783519035428
- ↑ 2.0 2.1 2.2 Entry on Chinolizidin-Alkaloide. at: Römpp Online. Georg Thieme Verlag, retrieved 28. April 2020.
- ↑ Ma, Xiaoqiang; Gang, David R. (2004). "The Lycopodium alkaloids". Natural Product Reports 21 (6): 752–772. doi:10.1039/b409720n. PMID 15565253.
- ↑ D. Knöfel, H. Schütte (1970), "Chinolizidinalkaloide: Konstitution und Konfiguration von Tinctorin aus Genista tinctoria" (in German), Journal fur praktische Chemie 312 (5): pp. 887f., doi:10.1002/prac.19703120521
- ↑
- Kaiser, Natalie; Douches, David; Dhingra, Amit; Glenn, Kevin C.; Herzig, Philip Reed; Stowe, Evan C.; Swarup, Shilpa (2020). "The role of conventional plant breeding in ensuring safe levels of naturally occurring toxins in food crops". Trends in Food Science and Technology (EFSA & IUFoST (Elsevier)) 100: 51–66. doi:10.1016/j.tifs.2020.03.042. ISSN 0924-2244.
- Sadras, Victor; Calderini, Daniel (2021). Crop Physiology : Case Histories for Major Crops. Amsterdam. pp. xxi+756. doi:10.1016/c2018-0-05018-5. ISBN 978-0-12-819195-8. OCLC 1225947369.(pp430-450)
- Gulisano, Agata; Alves, Sofia; Martins, João Neves; Trindade, Luisa M. (2019-10-30). "Genetics and Breeding of Lupinus mutabilis: An Emerging Protein Crop". Frontiers in Plant Science (Frontiers) 10: 1385. doi:10.3389/fpls.2019.01385. ISSN 1664-462X. PMID 31737013.
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