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Substrate Report for: Me-GlcA-X

Name Class
Me-GlcA-XTypeGlucuronoyl
Carbohydrate
Glycoside
Other_Namemethyl(5-Bromo-4-chloro-3-indolyl beta-d-glucuronide)uronate
Chemical_NomenclatureMethyl (5-bromo-4-chloro-3-indolyl beta-D-glucopyranosid)uronate
FormulaC15H15BrClNO7
MW436.64
PaperFranova_2016_Anal.Biochem_510_114
Kiernan_2007_Biotech.Histochem_82_73
CommentWhen hydrolysed by Glucuronoyl_esterase (removal of the methyl group) gives a chromogenic substrate for beta-Glucuronidase. The product 5-bromo-4-chloro-3-indolyl react rapidly with oxygen to yield insoluble blue indigo
FamilyGlucuronoyl_esterase
InChIKeyHKXDXRGOJKQXDY-UHFFFAOYSA-N
CanonicalSMILESC1(C(C(C(C(O1)OC2=C[N]C3=CC=C(C(=C23)Cl)Br)O)O)O)C(=O)OC
InChIInChI=1S/C15H15BrClNO7/c1-23-14(22)13-11(20)10(19)12(21)15(25-13)24-7-4-18-6-3-2-5(16)9(17)8(6)7/h2-4,10-13,15,18-21H,1H3

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Please cite: Lenfant 2013 Nucleic.Acids.Res. or Marchot Chatonnet 2012 Prot.Pept Lett.
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