Мы используем файлы cookie.
Продолжая использовать сайт, вы даете свое согласие на работу с этими файлами.
Продолжая использовать сайт, вы даете свое согласие на работу с этими файлами.
Azirinomycin
Подписчиков: 0, рейтинг: 0
Names | |
---|---|
IUPAC name
3-Methyl-2H-azirine-2-carboxylic acid
| |
Identifiers | |
3D model (JSmol)
|
|
PubChem CID
|
|
CompTox Dashboard (EPA)
|
|
| |
| |
Properties | |
C4H5NO2 | |
Molar mass | 99.089 g·mol−1 |
Related compounds | |
Related compounds
|
Azirine Motualevic acid F |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Azirinomycin is an antibiotic azirine derivative with the molecular formula C4H5NO2 which is produced by the bacterium Streptomyces aureus. Azirinomycin was first isolated in 1971. Azirinomycin is toxic and therefore it cannot not be used in human medicine.
Further reading
- Miller, TW; Tristram, EW; Wolf, FJ (January 1971). "Azirinomycin. II. Isolation and chemical characterization as 3-methyl-2(2H) azirinecarboxylic acid". The Journal of Antibiotics. 24 (1): 48–50. doi:10.7164/antibiotics.24.48. PMID 5541332.
- Stapley, EO; Hendlin, D; Jackson, M; Miller, AK; Hernandez, S; Mata, JM (January 1971). "Azirinomycin. I. Microbial production and biological characteristics". The Journal of Antibiotics. 24 (1): 42–7. doi:10.7164/antibiotics.24.42. PMID 5541331.
- Williams, R. M. (22 October 2013). Synthesis of Optically Active Alpha-Amino Acids. Elsevier. p. 126. ISBN 978-1-4832-9295-3.
- Carreira, Erick M. (14 May 2014). Science of Synthesis Knowledge Updates 2011 Vol. 3. Georg Thieme Verlag. p. 137. ISBN 978-3-13-178751-4.