To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

How to transfigure the Wikipedia

Would you like Wikipedia to always look as professional and up-to-date? We have created a browser extension. It will enhance any encyclopedic page you visit with the magic of the WIKI 2 technology.

Try it — you can delete it anytime.

Install in 5 seconds
4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
Great Wikipedia has got greater.
.
Leo
Newton
Brights
Milds

3-Deoxy-D-manno-oct-2-ulosonic acid

From Wikipedia, the free encyclopedia

3-Deoxy-d-manno-oct-2-ulosonic acid
Names
IUPAC name
(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
3D model (JSmol)
Abbreviations D-KDO; KDO; dOclA
ChEBI
ChemSpider
UNII
  • InChI=1S/C8H14O8/c9-2-5(12)7(14)6(13)3(10)1-4(11)8(15)16/h3,5-7,9-10,12-14H,1-2H2,(H,15,16)/t3-,5-,6-,7-/m1/s1 checkY
    Key: KYQCXUMVJGMDNG-SHUUEZRQSA-N checkY
  • InChI=1/C8H14O8/c9-2-5(12)7(14)6(13)3(10)1-4(11)8(15)16/h3,5-7,9-10,12-14H,1-2H2,(H,15,16)/t3-,5-,6-,7-/m1/s1
    Key: KYQCXUMVJGMDNG-SHUUEZRQBC
  • O[C@@H]([C@@H]([C@@H](CC(C(O)=O)=O)O)O)[C@H](O)CO
  • O=C(O)C(=O)C[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
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).
☒N verify (what is checkY☒N ?)

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.

The cyclization of 3-deoxy-d-manno-oct-2-ulosonic acid to the β-anomer. The chiral centers are indicated by asterisks.

References

  1. ^ 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.


Stub icon

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

This page was last edited on 18 March 2021, at 18:13
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.
Contact WIKI 2
Introduction
Terms of Service
Privacy Policy