Chemistry:Salbostatin
From HandWiki
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| IUPAC name
(1S,2S,3R,6S)-6-[[(3S,4R,5S,6R)-4,5-Dihydroxy-6-(hydroxymethyl)oxan-3-yl]amino]-4-(hydroxymethyl)cyclohex-4-ene-1,2,3-triol
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3D model (JSmol)
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| Properties | |
| C13H23O8 | |
| Molar mass | 307.319 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Salbostatin is an antibiotic and trehalase inhibitor with the molecular formula C13H23O8.[1][2][3][4] Salbostatin is produced by the bacterium Streptomyces albus.[5]
References
- ↑ Lorbach, Volker (2007) (in de). Von Chorismat abgeleitete funktionalisierte Cyclohexadiene: Verwendung als chirale Synthesebausteine und Erweiterung der mikrobiell zugänglichen Produktpalette um einen Aminoalkohol. Forschungszentrum Jülich. p. 98. ISBN 978-3-89336-500-5.
- ↑ Chapleur, Yves (10 September 1998) (in en). Carbohydrate Mimics: Concepts and Methods. Wiley. p. 91. ISBN 978-3-527-29526-5.
- ↑ Fugmann, Burkhard (14 May 2014) (in de). RÖMPP Lexikon Naturstoffe, 1. Auflage, 1997. Georg Thieme Verlag. p. 565. ISBN 978-3-13-179291-4.
- ↑ Yamagishi, Tatsuya; Uchida, Chikara; Ogawa, Seiichiro (2 March 1995). "Total synthesis of trehalase inhibitor salbostatin" (in en). Bioorganic & Medicinal Chemistry Letters 5 (5): 487–490. doi:10.1016/0960-894X(95)00055-X. ISSN 0960-894X.
- ↑ Vértesy, L.; Fehlhaber, H.; Schulz, A. (1994). "The Trehalase Inhibitor Salbostatin, a Novel Metabolite from Streptomyces albus, ATCC21838". Angew. Chem. Int. Ed. 33 (18): 1844–1846. doi:10.1002/ANIE.199418441.
Further reading
- (in en) Studies in Natural Products Chemistry. Elsevier. 29 November 2018. p. 141. ISBN 978-0-444-64182-3.
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