43:
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560:"The biosynthesis of cell wall lipopolysaccharide in Escherichia coli. III. The isolation and characterization of 3-deoxyoctulosonic acid"
17:
639:
315:
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670:
632:
324:
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
620:
334:
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
257:
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42:
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8:
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513:
prefix indicates that the four chiral centers have the same configuration as
490:
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558:
Ghalambor, Mohammad Ali; Levine, Edward M.; Heath, Edward C. (1966).
420:
Except where otherwise noted, data are given for materials in their
604:
498:
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155:
284:
657:
540:. The chiral centers are indicated by asterisks.
245:
140:
640:
75:)-4,5,6,7,8-pentahydroxy-2-oxooctanoic acid
647:
633:
299:
220:
575:
265:
523:
295:
14:
658:
327:Key: KYQCXUMVJGMDNG-SHUUEZRQSA-N
200:
599:
337:Key: KYQCXUMVJGMDNG-SHUUEZRQBC
236:
24:
25:
682:
603:
428:
390:
41:
564:Journal of Biological Chemistry
424:(at 25 °C , 100 kPa).
551:
536:-oct-2-ulosonic acid to the β-
396:
384:
13:
1:
577:10.1016/S0021-9258(18)96516-6
544:
619:. You can help Knowledge by
7:
528:The cyclization of 3-deoxy-
10:
687:
598:
363:O=C(O)C(=O)C(O)(O)(O)(O)CO
358:O(((CC(C(O)=O)=O)O)O)(O)CO
418:
371:
346:
311:
124:
109:-manno-2-octulosonic acid
80:
54:
49:
40:
18:Ketodeoxyoctulosonic acid
671:Organic compound stubs
611:This article about an
541:
527:
475:ketodeoxyoctonic acid
36:-oct-2-ulosonic acid
501:in the synthesis of
471:-oct-2-ulosonic acid
503:lipopolysaccharides
414: g·mol
270: (linear form)
145: (linear form)
103:-mannooctanoic acid
37:
542:
451:Infobox references
187:D-KDO; KDO; dOclA
87:-mannooctonic acid
27:
628:
627:
497:which is used by
459:Chemical compound
457:
456:
280:CompTox Dashboard
174:Interactive image
167:Interactive image
119:-octulosonic acid
16:(Redirected from
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613:organic compound
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379:Chemical formula
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570:(13): 3207–15.
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297:DTXSID501265068
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99:2-Keto-3-deoxy-
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90:
89:2-Keto-3-Deoxy-
88:
84:
76:
29:
23:
22:
15:
12:
11:
5:
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422:standard state
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184:Abbreviations
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146:
137:
135:
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83:2-Oxo-3-deoxy-
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78:
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58:
52:
51:
47:
46:
9:
6:
4:
3:
2:
683:
672:
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561:
554:
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539:
535:
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520:
512:
504:
500:
496:
492:
491:ulosonic acid
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476:
472:
470:
452:
445:
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423:
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118:
96:
79:
74:
70:
66:
62:
57:
53:
48:
44:
39:
35:
19:
621:expanding it
610:
595:
567:
563:
553:
533:
510:
495:2-ketooctose
486:
478:
474:
468:
462:
461:
125:Identifiers
116:
94:
81:Other names
72:
68:
64:
60:
33:
666:Sugar acids
372:Properties
202:CHEBI:32817
660:Categories
545:References
407:Molar mass
267:ZWK96OG89F
213:ChemSpider
154:3D model (
142:10149-14-1
132:CAS Number
56:IUPAC name
97:-octonate
499:bacteria
489:) is an
463:3-Deoxy-
111:3-Deoxy-
105:3-Deoxy-
28:3-Deoxy-
586:4287911
519:mannose
485:symbol
444:what is
442: (
412:238.192
234:PubChem
584:
538:anomer
505:. The
439:verify
436:
351:SMILES
247:445569
222:106511
50:Names
615:is a
534:manno
511:manno
493:of a
483:IUPAC
469:manno
316:InChI
193:ChEBI
156:JSmol
117:manno
95:manno
34:manno
617:stub
582:PMID
258:UNII
572:doi
568:241
487:Kdo
479:KDO
285:EPA
237:CID
662::
580:.
566:.
562:.
521:.
481:;
477:;
394:14
71:,7
67:,6
63:,5
59:(4
648:e
641:t
634:v
623:.
588:.
574::
532:-
530:d
517:-
515:d
509:-
507:d
473:(
467:-
465:d
434:N
400:8
397:O
391:H
388:8
385:C
287:)
283:(
158:)
115:-
113:d
107:d
101:d
93:-
91:d
85:d
73:R
69:R
65:R
61:R
32:-
30:d
20:)
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