4-Methylumbelliferyl nonanoate
4-Mu-Nonanoate; Nonanoic acid 4-methylumbelliferyl ester
4-Methylumbelliferyl nonanoate is a synthetic substrate that can be used in the study of glycoconjugates. It reacts with taurocholate to form an activated ester, which can be used to measure the activity of various enzymes. This compound has been shown to be a functional probe for bladder cancer and has been used as a synthetic substrate in studies of oligosaccharides. 4-Methylumbelliferyl nonanoate is also able to detect glycoconjugates on cells, including those found in cancerous tissues. This molecule has been used to analyze the distribution of glycoproteins on cell surfaces by fluorimetric chromatography.
CAS Number | 18319-93-2 |
Product Name | 4-Methyl-2-oxo-2H-1-benzopyran-7-yl nonan-1-oate |
IUPAC Name | (4-methyl-2-oxochromen-7-yl) nonanoate |
Molecular Formula | C19H24O4 |
Molecular Weight | 316.4 g/mol |
InChI | InChI=1S/C19H24O4/c1-3-4-5-6-7-8-9-18(20)22-15-10-11-16-14(2)12-19(21)23-17(16)13-15/h10-13H,3-9H2,1-2H3 |
InChI Key | IEJIWAFZZKFSFV-UHFFFAOYSA-N |
SMILES | CCCCCCCCC(=O)OC1=CC2=C(C=C1)C(=CC(=O)O2)C |
Canonical SMILES | CCCCCCCCC(=O)OC1=CC2=C(C=C1)C(=CC(=O)O2)C |