EC Number |
Substrates |
Organism |
Products |
Reversibility |
---|
3.2.1.76 | 2,5-anhydro-3-O-alpha-L-idopyranuronosyl-D-mannitol + H2O |
- |
Homo sapiens |
? |
- |
? |
3.2.1.76 | 2,5-anhydro-4-O-alpha-L-idopyranuronosyl-D-mannitol 6-sulfate + H2O |
- |
Homo sapiens |
? |
- |
? |
3.2.1.76 | 4-methylcoumarin-7-yl-alpha-L-iduronic acid + H2O |
design and development of an improved and less expensive synthesis method for the fluorogenic substrate, overview. The method is based on the double ketal fixation of the 1,2 and 3,5-hydroxy groups of D-glucose to form a cis-anti-cis-fused tricyclic D-glucofuranosyl derivative, which could undergo elimination to form a 5-exo-double bond followed by electrophilic addition, a Mitsunobu-type glycosylation reaction is used for the coupling of the hemiacetal with the acceptor |
Homo sapiens |
4-methylcoumarin + alpha-L-iduronic acid |
- |
? |
3.2.1.76 | 4-methylumbelliferyl alpha-L-iduronide + H2O |
- |
Homo sapiens |
4-methylumbelliferone + alpha-L-iduronic acid |
- |
? |
3.2.1.76 | 4-methylumbelliferyl-alpha-L-iduronide + H2O |
- |
Homo sapiens |
? |
- |
? |
3.2.1.76 | 4-methylumbelliferyl-alpha-L-iduronide + H2O |
- |
Rattus norvegicus |
? |
- |
? |
3.2.1.76 | 4-methylumbelliferyl-alpha-L-iduronide + H2O |
- |
Sus scrofa |
? |
- |
? |
3.2.1.76 | 4-methylumbelliferyl-alpha-L-iduronide + H2O |
- |
Bos taurus |
? |
- |
? |
3.2.1.76 | 4-methylumbelliferyl-alpha-L-iduronide + H2O |
- |
Mus musculus |
4-methylumbelliferone + alpha-L-iduronic acid |
- |
? |
3.2.1.76 | 4-methylumbelliferyl-alpha-L-iduronide + H2O |
- |
Homo sapiens |
4-methylumbelliferone + alpha-L-iduronic acid |
- |
? |