32449-92-6
Chemical Structure
D-Glucuronic acid lactone
Synonym(s): D-Glucurono-6,3-lactone; D-Glucurono-γ-lactone; D-Glucuronolactone; Dicurone; Glucoxy; Glucurolactone; Glucurone
- CAS No.: 32449-92-6
- Formula:C6H8O6
- Molecular Weight:176.12
IUPAC Name: (R)-2-((2S,3R,4S)-3,4-dihydroxy-5-oxotetrahydrofuran-2-yl)-2-hydroxyacetaldehyde
InChIKey: UYUXSRADSPPKRZ-SKNVOMKLSA-N
SMILES: O=C1[C@@H](O)[C@@H](O)[C@]([C@@H](O)C=O)([H])O1
Biological Activity: D-Glucuronic acid lactone (D-Glucurono-6,3-lactone; D-Glucurono-γ-lactone; D-Glucuronolactone; Dicurone; Glucoxy; Glucurolactone; Glucurone) is an endogenous metabolite and a glucuronic acid derivative. D-Glucuronic acid lactone serves as a starting reagent for the synthesis of 2,3,4-tris (tert-butyldimethylsilyl) glucuronic acid trichloroethyl ester, which is used to prepare 1-O-acyl glucuronic acids for the anti-inflammatory agent mL-3000 (HY-B1452), synthesize optically active glucuronic acids, and produce long-chain alkyl glucuronides. D-Glucuronic acid lactone shows potential for use in studies of reversible cerebral vasoconstriction syndrome (RCVS)[1][2][3].
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D-Glucuronic acid lactone | 98.0% | D-Glucuronic acid lactone (D-Glucurono-6,3-lactone; D-Glucurono-γ-lactone; D-Glucuronolactone; Dicurone; Glucoxy; Glucurolactone; Glucurone) is an endogenous metabolite and a glucuronic acid derivative. D-Glucuronic acid lactone serves as a starting reagent for the synthesis of 2,3,4-tris (tert-butyldimethylsilyl) glucuronic acid trichloroethyl ester, which is used to prepare 1-O-acyl glucuronic acids for the anti-inflammatory agent mL-3000 (HY-B1452), synthesize optically active glucuronic acids, and produce long-chain alkyl glucuronides. D-Glucuronic acid lactone shows potential for use in studies of reversible cerebral vasoconstriction syndrome (RCVS). | ||||||||||||||||||||
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D-Glucuronic acid lactone (Standard) | 99.96% | D-Glucuronic acid lactone (Standard) is the analytical standard of D-Glucuronic acid lactone. This product is intended for research and analytical applications. D-Glucuronic acid lactone is an endogenous metabolite. | ||||||||||||||||||||
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- [1]. Florio P, et al. Rapid access to uronic acid-based mimetics of Kdn2en from D-glucurono-6,3-lactone. Carbohydr Res. 2000;328(4):445-448. [Content Brief]
- [2]. Dr. Wilhelm V. Dahlhoff, et al. L-Gulose or D-gluco-Hexodialdose from D-Glucurono-6,3-lactone by Controlled Reductions. Verlag Chemie. GmbH. 6940 Weinheim, 1980
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[3]. Đorđe Glišin, et al. D-GLUCURONO-6,3-LACTONE AS AN INTERESTING COMPOUND IN THE SYNTHETIC CHEMISTRY OF CARBOHYDRATES RELATED TARGETS. (SHORT COMMUNICATION)
UDC 547.454:542.913
