Chemistry:3-Deoxy-D-manno-oct-2-ulosonic acid
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Revision as of 07:11, 29 June 2021 by imported>NBrushPhys (fix)
Names | |
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IUPAC name
(4R,5R,6R,7R)-4,5,6,7,8-pentahydroxy-2-oxooctanoic acid
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Other names
2-Oxo-3-deoxy-d-mannooctonic acid
2-Keto-3-Deoxy-d-manno-octonate 2-Keto-3-deoxy-d-mannooctanoic acid 3-Deoxy-d-manno-2-octulosonic acid 3-Deoxy-d-manno-octulosonic acid | |
Identifiers | |
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3D model (JSmol)
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Abbreviations | D-KDO; KDO; dOclA |
ChEBI | |
ChemSpider | |
PubChem CID
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UNII |
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Properties | |
C8H14O8 | |
Molar mass | 238.192 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Tracking categories (test):
3-Deoxy-d-manno-oct-2-ulosonic acid (ketodeoxyoctonic acid; KDO; IUPAC symbol Kdo) is an ulosonic acid of a 2-ketooctose which is used by bacteria in the synthesis of lipopolysaccharides.[1] The d-manno prefix indicates that the four chiral centers have the same configuration as d-mannose.
References
- ↑ Ghalambor, Mohammad Ali; Levine, Edward M.; Heath, Edward C. (1966). "The biosynthesis of cell wall lipopolysaccharide in Escherichia coli. III. The isolation and characterization of 3-deoxyoctulosonic acid". Journal of Biological Chemistry 241 (13): 3207–15. doi:10.1016/S0021-9258(18)96516-6. PMID 4287911.
Original source: https://en.wikipedia.org/wiki/3-Deoxy-D-manno-oct-2-ulosonic acid.
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