3-Deoxy-D-manno-oct-2-ulosonic acid
3-Deoxy-D-manno-oct-2-ulosonic acid | |
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(4R,5R,6R,7R)-4,5,6,7,8-pentahydroxy-2-oxooctanoic acid | |
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 | |
Abbreviations | D-KDO; KDO; dOclA |
CAS number | 10149-14-1, linear form |
PubChem | 445569 |
ChemSpider | 106511 |
ChEBI | CHEBI:32817 |
Jmol-3D images | {{#if:O[C@@H]([C@@H]([C@@H](CC(C(O)=O)=O)O)O)[C@H](O)COO=C(O)C(=O)C[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO|Image 1 Image 2 |
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Properties | |
Molecular formula | C8H14O8 |
Molar mass | 238.19 g mol−1 |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
Infobox references | |
3-Deoxy-D-manno-oct-2-ulosonic acid or 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 four chiral centers have the same configuration as D-mannose.