Angustmycin A
Appearance
Names | |
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IUPAC name
2-(6-aminopurin-9-yl)-2-(hydroxymethyl)-5-methylideneoxolane-3,4-diol[1]
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Other names
Decoyinine
4′,5′-Didehydro-1′-C-(hydroxymethyl)adenosine | |
Identifiers | |
3D model (JSmol)
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ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.213.257 |
EC Number |
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PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C11H13N5O4 | |
Molar mass | 279.256 g·mol−1 |
Hazards | |
GHS labelling:[2] | |
Warning | |
H315, H319, H335 | |
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Angustmycin A is a purine antibiotic and metabolite from Streptomyces bacteria with the molecular formula C11H13N5O4.[3][1] Angustmycin A is also a cytokinin.[4][5][6]
References
[edit]- ^ a b "Angustmycin A". Pubchem.ncbi.NLM.nih.gov.
- ^ "Decoyinine". pubchem.ncbi.nlm.nih.gov. Retrieved 18 May 2022.
- ^ Scott, Thomas (20 January 2020). Concise encyclopedia of biochemistry. Walter de Gruyter GmbH & Co KG. p. 32. ISBN 978-3-11-171099-0.
- ^ Yu, Le; Zhou, Wenting; She, Yixuan; Ma, Hongmin; Cai, You-Sheng; Jiang, Ming; Deng, Zixin; Price, Neil P. J.; Chen, Wenqing (17 November 2021). "Efficient biosynthesis of nucleoside cytokinin angustmycin A containing an unusual sugar system". Nature Communications. 12 (1): 6633. Bibcode:2021NatCo..12.6633Y. doi:10.1038/s41467-021-26928-y. ISSN 2041-1723. PMC 8599513. PMID 34789759.
- ^ Gottlieb, David; Shaw, Paul D. (6 December 2012). Mechanism of Action. Springer Science & Business Media. p. 465. ISBN 978-3-642-46051-7.
- ^ Korzybski, Tadeusz; Kowszyk-Gindifer, Zuzanna; Kurylowicz, Wlodzimierz (3 September 2013). Antibiotics: Origin, Nature and Properties. Elsevier. ISBN 978-1-4832-2305-6.
Further reading
[edit]- Hoeksema, H.; Slomp, G.; van Tamelen, E. E. (1 January 1964). "Angustmycin A and decoyinine". Tetrahedron Letters. 5 (27): 1787–1795. doi:10.1016/S0040-4039(01)89489-2. ISSN 0040-4039.
- McCarthy, James R.; Robins, Roland K.; Robins, Morris J. (August 1968). "Purine nucleosides. XXII. Synthesis of angustmycin A (decoyinine) and related unsaturated nucleosides". Journal of the American Chemical Society. 90 (18): 4993–4999. doi:10.1021/ja01020a038. PMID 5665542.