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street names for ketamine (同)jet, super acid, special K, honey oil, green, cat valium, super C
the 11th letter of the Roman alphabet (同)k

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/12/25 00:40:39」(JST)

Synthesis of Chlamydia Lipopolysaccharide Haptens through the use of α-Specific 3-Iodo-Kdo Fluoride Glycosyl Donors.

Pokorny B1, Kosma P.
Chemistry (Weinheim an der Bergstrasse, Germany).Chemistry.2014 Oct 29. doi: 10.1002/chem.201405424. [Epub ahead of print]
A scalable approach towards high-yielding and (stereo)selective glycosyl donors of the 2-ulosonic acid Kdo (3-deoxy-D-manno-oct-2-ulosonic acid) is a fundamental requirement for the development of vaccines against Gram-negative bacteria. Herein, we disclose a short synthetic route to 3-iodo Kdo fluo
PMID 25354167

Impact of conjugation chemistry on the immunogenicity of S. Typhimurium conjugate vaccines.

Stefanetti G1, Rondini S1, Lanzilao L1, Saul A1, MacLennan CA1, Micoli F2.
Vaccine.Vaccine.2014 Oct 21;32(46):6122-9. doi: 10.1016/j.vaccine.2014.08.056. Epub 2014 Sep 3.
Salmonella Typhimurium is major cause of invasive nontyphoidal Salmonella disease in Africa. Conjugation of S. Typhimurium O-antigen to an appropriate carrier protein constitutes a possible strategy for the development of a vaccine against this disease, for which no vaccines are currently available.
PMID 25192974

Structural analysis of arabinose-5-phosphate isomerase from Bacteroides fragilis and functional implications.

Chiu HJ, Grant JC, Farr CL, Jaroszewski L, Knuth MW, Miller MD, Elsliger MA, Deacon AM, Godzik A, Lesley SA, Wilson IA.
Acta crystallographica. Section D, Biological crystallography.Acta Crystallogr D Biol Crystallogr.2014 Oct 1;70(Pt 10):2640-51. doi: 10.1107/S1399004714017052. Epub 2014 Sep 27.
The crystal structure of arabinose-5-phosphate isomerase (API) from Bacteroides fragilis (bfAPI) was determined at 1.7 Å resolution and was found to be a tetramer of a single-domain sugar isomerase (SIS) with an endogenous ligand, CMP-Kdo (cytidine 5'-monophosphate-3-deoxy-D-manno-oct-2-ulosonate
PMID 25286848

4-2-10 ホウ素ラムノガラクツロナンII複合体の機能に関する研究 : 特異的構成糖KDOの合成経路とその変異株の解析(4-2 植物の微量栄養素,2015年度京都大会)

Sugar Activation for Production of Nucleotide Sugars as Substrates for Glycosyltransferases in Plants

リンク元	「3-デオキシ-D-マンノオクツロソン酸」
関連記事	「KD」「K」

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
CAS Number	10149-14-1 linear form
Abbreviations	D-KDO; KDO; dOclA
ChEBI	CHEBI:32817
ChemSpider	106511
Jmol interactive 3D	Image; Image
PubChem	445569
	InChI 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 Key: KYQCXUMVJGMDNG-SHUUEZRQSA-N ; 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 ;
	SMILES 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
Chemical formula	C8H14O8
Molar mass	238.19 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references