Kopsanone
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| Names | |
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| IUPAC name
5,14-diazaheptacyclo[12.5.3.01,13.04,12.04,18.06,11.012,16]docosa-6,8,10-trien-17-one
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| Other names
Kopsan-22-one
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| Identifiers | |
3D model (
JSmol ) |
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| ChemSpider | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C20H22N2O | |
| Molar mass | 306.409 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Kopsanone is an alkaloid isolated from Aspidosperma.[1]
References
- PMID 17252481.
Extra reading
- Klein-Júnior, Lc; Bannwart, G; Kato, L; Oliveira, Cma; Gontijo, B; Silva, Cc; Ferreira, Hd; Vander Heyden, Y; Passos, Cs; Henriques, At; Santin, Smo (25 November 2015). "Kopsanone and N(4)-oxide-kopsanone: two β-carbolinic indole alkaloids with monoamine oxidase A inhibitory activity". Planta Medica. 81 (16): s–0035–1565743. .
- Craven, B. M. (1 October 1969). "The crystal structure and absolute configuration of the N ( b )-methiodide of (−)-kopsanone". Acta Crystallographica Section B: Structural Crystallography and Crystal Chemistry. 25 (10): 2131–2139. .
- Leng, Lingying; Zhou, Xiaohan; Liao, Qi; Wang, Falu; Song, Hao; Zhang, Dan; Liu, Xiao-Yu; Qin, Yong (20 March 2017). "Asymmetric Total Syntheses of Kopsia Indole Alkaloids". Angewandte Chemie International Edition. 56 (13): 3703–3707. .
- Layne, Tanya H.; Roach, Joy S.; Tinto, Winston F. (January 2015). "Review of β-carboline Alkaloids from the Genus Aspidosperma". Natural Product Communications. 10 (1): 1934578X1501000.
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