글루론산

글루론산
글루론산 구조식 이미지
카스 번호:
15769-56-9
한글명:
글루론산
동의어(한글):
글루론산
상품명:
guluronic acid
동의어(영문):
G2013;guluronic acid;Einecs 239-860-9;Guluronic acid sodium salt;L-Guluronic Acid Sodium Salt/Guluronic acid;L-Monoguluronic Acid Sodium Salt, Mono-Guluronic Acid Sodium Salt
CBNumber:
CB8930228
분자식:
C6H10O7
포뮬러 무게:
194.14
MOL 파일:
15769-56-9.mol

글루론산 속성

물리적 상태
Solid
색상
White to off-white
InChI
InChI=1S/C6H10O7/c7-1-2(8)3(9)4(10)5(11)6(12)13/h1-5,8-11H,(H,12,13)/t2-,3-,4+,5-/m0/s1
InChIKey
IAJILQKETJEXLJ-KLVWXMOXSA-N
SMILES
O=C[C@@H]([C@@H]([C@H]([C@@H](C(O)=O)O)O)O)O

안전

글루론산 C화학적 특성, 용도, 생산

개요

Glucuronic acid is a sugar acid derived from glucose, with its sixth carbon atom oxidized to a carboxylic acid. In living beings, this primary oxidation occurs with UDP-α-D-glucose (UDPG), not with the free sugar.
Glucuronic acid, like its precursor glucose, can exist as a linear (carboxo-)aldohexose (<1%), or as a cyclic hemiacetal (furanose or pyranose). Aldohexoses such as D-glucose are capable of forming two furanose forms (α and β) and two pyranose forms (α and β). By the Fischer convention, glucuronic acid has two stereoisomers (enantiomers), D- and L-glucuronic acid, depending on its configuration at C-5. Most physiological sugars are of the D-configuration. Due to ring closure, cyclic sugars have another asymmetric carbon atom (C-1), resulting in two more stereoisomers, named anomers. Depending on the configuration at C-1, there are two anomers of glucuronic acid, α- and β-form. In β-D-glucuronic acid the C-1 hydroxy group is on the same side of the pyranose ring as the carboxyl group. In the free sugar acid, the β-form is prevalent (~64%), whereas in the organism, the α-form UDP-α-D-glucuronic acid (UDPGA) predominates.

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