Valienamine
 | |
| Names | |
|---|---|
| IUPAC name
(1S,2S,3R,6S)-6-amino-4-(hydroxymethyl)cyclohex-4-ene-1,2,3-triol | |
| Identifiers | |
38231-86-6  | |
| ChEMBL | ChEMBL1230806 |
| ChemSpider | 168149  |
| |
| Jmol-3D images | Image |
| PubChem | 193758 |
| |
| Properties | |
| C7H13NO4 | |
| Molar mass | 175.18 g/mol |
| Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
| verify (what is: /?) | |
| Infobox references | |
Valienamine is a C-7 aminocyclitol found as a substructure of pseudooligosaccharides such as acarbose or validamycins. It can be found in Actinoplanes species.[1]
It is an intermediate formed by microbial degradation of validamycins.[2]
References
- ↑ Zhang CS, Stratmann A, Block O et al. (June 2002). "Biosynthesis of the C(7)-cyclitol moiety of acarbose in Actinoplanes species SE50/110. 7-O-phosphorylation of the initial cyclitol precursor leads to proposal of a new biosynthetic pathway". J. Biol. Chem. 277 (25): 22853–62. doi:10.1074/jbc.M202375200. PMID 11937512.
- ↑ PubChem 193758