54322-38-2
Chemical Structure
4-Methylumbelliferyl α-L-fucopyranoside
- CAS No.: 54322-38-2
- Formula:C16H18O7
- Molecular Weight:322.31
IUPAC Name: 4-methyl-7-(((2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-2H-chromen-2-one
InChIKey: CQKHENXHLAUMBH-CRLRYRHBSA-N
SMILES: CC(C1=CC=C(O[C@H]2[C@H]([C@@H]([C@@H]([C@@H](O2)C)O)O)O)C=C1O3)=CC3=O
Biological Activity: 4-Methylumbelliferyl α-L-fucopyranoside is an α-L-fucosidase. α-L-fucosidase can enhance capacitation of porcine sperm and protect sperm from premature acrosome reaction. Compared with human liver α-L-fucosidase, 4-Methylumbelliferyl α-L-fucopyranoside has considerable hydrophobicity and isoelectric focusing properties[1][2].
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4-Methylumbelliferyl α-L-fucopyranoside | 4-Methylumbelliferyl α-L-fucopyranoside is an α-L-fucosidase. α-L-fucosidase can enhance capacitation of porcine sperm and protect sperm from premature acrosome reaction. Compared with human liver α-L-fucosidase, 4-Methylumbelliferyl α-L-fucopyranoside has considerable hydrophobicity and isoelectric focusing properties. | |||||||||||||||||||||
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References
- [1]. Hopfer RL, et al. Solubilization and characterization of pellet-associated human brain alpha-L-fucosidase activity. Biochem J. 1985 Aug 1;229(3):679-85. [Content Brief]
- [2]. Romero-Aguirregomezcorta J, et al. α-L-fucosidase enhances capacitation-associated events in porcine spermatozoa. Vet J. 2015 Jan;203(1):109-14. [Content Brief]
