InChI=1S/C16H18O8/c1-7-4-12(18)23-10-5-8(2-3-9(7)10)22-16-15(21)14(20)13(19)11(6-17)24-16/h2-5,11,13-17,19-21H,6H2,1H3/t11-,13+,14+,15-,16-/m1/s1 |
YUDPTGPSBJVHCN-DZQJYWQESA-N |
O(C=1C=C2OC(=O)C=C(C2=CC1)C)[C@H]3[C@@H]([C@@H](O)[C@H]([C@H](O3)CO)O)O |
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chromogenic compound
Colourless, endogenous or exogenous pigment precursors that may be transformed by biological mechanisms into coloured compounds. They are used in biochemical assays and in diagnosis as indicators, particularly in the form of enzyme substrates.
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View more via ChEBI Ontology
4-methyl-2-oxo-2H-1-benzopyran-7-yl β-D-galactopyranoside
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4-Methylumbelliferyl beta-galactoside
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ChemIDplus
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4-Methylumbelliferyl-galactopyranoside
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ChemIDplus
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7-(beta-D-Galactopyranosyloxy)-4-methyl-2H-1-benzopyran-2-one
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ChemIDplus
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6160-78-7
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CAS Registry Number
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ChemIDplus
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94673
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Reaxys Registry Number
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Reaxys
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HEYWORTH R, DAHLQVIST A (1962) Pig intestinal beta-glucosidase activities. II. Evidence for the hydrolysis of 4-methylumbelliferyl beta-D-glucoside and beta-D-galactoside at the same enzyme site. Biochimica et biophysica acta 64, 182-184 [PubMed:13954348] |
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