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Inhibitor Report for: D-glucuronate

product of hydrolysis of Glucuronoyl ester. enantiomer of a L-glucopyranuronic acid


General
Type Glucuronoyl, Carbohydrate, Glycoside
Chemical_Nomenclature (2S,3S,4S,5R)-3,4,5,6-tetrahydroxyoxane-2-carboxylic acid
Canonical SMILES C1(C(C(OC(C1O)O)C(=O)O)O)O
InChI InChI=1S/C6H10O7/c7-1-2(8)4(5(10)11)13-6(12)3(1)9/h1-4,6-9,12H,(H,10,11)/t1-,2-,3+,4-,6?/m0/s1
InChIKey AEMOLEFTQBMNLQ-AQKNRBDQSA-N
Other name(s) D-Glucuronic acid ; DB01982 ; GCU ; Glucuronic Acid ; D-Glucopyranuronic Acid ; Glucuronate
________________________________________________________________________________________________
MW|194.14
Formula|C6H10O7
CAS_number|
PubChem|94715
UniChem|AEMOLEFTQBMNLQ-AQKNRBDQSA-N
IUPHAR|
Wikipedia|

Target
Families | D-glucuronate ligand of proteins in family: Glucuronoyl_esterase
Stucture | 1 structure: 6T0E: The glucuronoyl esterase OtCE15A S267A variant from Opitutus terrae in complex with benzyl D-glucuronoate and D-glucuronate
Protein | opitp-b1zmf4

References:
Search PubMed for references concerning: D-glucuronate
    Title: Structural and biochemical studies of the glucuronoyl esterase OtCE15A illuminate its interaction with lignocellulosic components
    Mazurkewich S, Poulsen JN, Lo Leggio L, Larsbrink J
    Ref: Journal of Biological Chemistry, 294:19978, 2019 : PubMed