α-galactosidase
Suppliers
Names
[ CAS No. ]:
9025-35-8
[ Name ]:
α-galactosidase
[Synonym ]:
Agalsidase
E.C. 3.2.1.22
alpha-Galactoside galactohydrolase
Melibiase
2-Quinoxalinecarbonyl chloride
quinoxaline-2-carbonyl chloride
alpha-D-Galactosidase
alpha-GAL 600L
alpha-D-Galactopyranosidase
Alpha-Gal 1000
Validase AGS
alpha-D-Galactoside galactohydrolase
Alpha Gal 500
alpha-Galactosidase A
Sumizyme AGS
Chemical & Physical Properties
[ Density]:
1.4±0.1 g/cm3
[ Boiling Point ]:
324.4±22.0 °C at 760 mmHg
[ Molecular Formula ]:
C9H5ClN2O
[ Molecular Weight ]:
192.602
[ Flash Point ]:
150.0±22.3 °C
[ Exact Mass ]:
192.009033
[ LogP ]:
2.12
[ Appearance of Characters ]:
buffered aqueous solution
[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C
[ Index of Refraction ]:
1.663
[ Storage condition ]:
2-8°C
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Hazard Codes ]:
Xi
[ Risk Phrases ]:
36/37/38
[ Safety Phrases ]:
36/37-26
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
Articles
Curr. Chem. Genomics 4 , 67-73, (2011)
Fabry disease is a rare X-linked lysosomal storage disorder caused by a deficiency in α-galactosidase A (GLA), which catalyzes the hydrolysis of terminal α-galactosyl groups from glycosphingolipids, s...
Am. J. Physiol. Gastrointest. Liver Physiol. 306(2) , G140-6, (2014)
A defect in the gene for the lysosomal enzyme α-galactosidase A (Gla) results in globotriaosylceramide (Gb3) accumulation in Fabry disease and leads to premature death from cardiac and cerebrovascular...
PLoS ONE 7(10) , e47805, (2012)
Enzyme replacement therapy (ERT) with alpha-Galactosidase A (aGal A) may cause antibody (AB) formation against aGal A in males with Fabry disease (FD). Anti agalsidase ABs negatively influence globotr...