InChI=1S/C19H28O14/c1- 2- 3- 29- 18(16(26) 27) 4- 8(21) 13(25) 15(33- 18) 11- 7- 30- 19(17(28) 31- 11) 5- 9(22) 12(24) 14(32- 19) 10(23) 6- 20/h2,8- 15,20- 25H,1,3- 7H2,(H,26,27) /p- 1/t8- ,9- ,10- ,11- ,12- ,13- ,14- ,15- ,18- ,19- /m1/s1 |
CCSZJBCZZCTGRR-XRXFFOJZSA-M |
OC[C@@H] (O) [C@H] 1O[C@@] 2(C[C@@H] (O) [C@H] 1O) OC[C@@H] (OC2=O) [C@H] 1O[C@@] (C[C@@H] (O) [C@H] 1O) (OCC=C) C([O- ] ) =O |
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Outgoing
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α- Kdo- (2→8)- α- Kdo- OAll(1−) II1,I7- lactone
(CHEBI:77925)
is a
carbohydrate acid derivative anion
(CHEBI:63551)
α- Kdo- (2→8)- α- Kdo- OAll(1−) II1,I7- lactone
(CHEBI:77925)
is conjugate base of
α-Kdo-(2→8)-α-Kdo-OAll II1,I7-lactone
(CHEBI:77926)
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Incoming
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sodium[α-Kdo-(2→8)-α-Kdo-OAll II1,I7-lactone]
(CHEBI:77923)
has part
α- Kdo- (2→8)- α- Kdo- OAll(1−) II1,I7- lactone
(CHEBI:77925)
α-Kdo-(2→8)-α-Kdo-OAll II1,I7-lactone
(CHEBI:77926)
is conjugate acid of
α- Kdo- (2→8)- α- Kdo- OAll(1−) II1,I7- lactone
(CHEBI:77925)
|
3- deoxy- α- D- manno- oct- 2- ulopyranonosyl- (2→8)- (prop- 2- en- 1- yl 3- deoxy- α- D- manno- oct- 2- ulopyranosid)onate
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(2R,4R,5R,6S)- 2- (allyloxy)- 6- {(3R,6R,8R,9R,10R)- 8- [(1R)- 1,2- dihydroxyethyl]- 9,10- dihydroxy- 5- oxo- 1,4,7- trioxaspiro[5.5]undec- 3- yl}- 4,5- dihydroxytetrahydro- 2H- pyran- 2- carboxylate
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IUPAC
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3- deoxy- α- D- manno- oct- 2- ulopyranonosyl- (2→8)- (allyl 3- deoxy- α- D- manno- oct- 2- ulopyranosid)onate II1,I7- lactone
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ChEBI
|
α- Kdo- (2→8)- α- Kdo- OAll(1−) II1,I7- lactone
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ChEBI
|
19665108
|
PubMed citation
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Europe PMC
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