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Agalsidase Beta

CAS No.
104138-64-9
Chemical Name:
Agalsidase Beta
Synonyms
Agalsidase Beta;Research Grade Fabrazyme/Agalsidase Alfa (DHC19529)
CBNumber:
CB82611282
Molecular Formula:
Molecular Weight:
0
MDL Number:
MOL File:
Mol file
Last updated:2023-05-04 17:34:31

Agalsidase Beta Properties

FDA UNII AGALSIDASE ALFA (2HLC17MX9G)
AGALSIDASE BETA (RZD65TSM9U)
ATC code A16AB04

Pharmacokinetic data

Protein binding 0%(Fabrazyme is a protein itself )
Excreted unchanged in urine Negligible
Volume of distribution 8.3-40.8 Litres
Biological half-life 45-100 minutes / No data

Agalsidase Beta price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0026510 AGALSIDASE BETA 95.00% 104138-64-9 5MG $501.34 2021-12-16 Buy
Product number Packaging Price Buy
API0026510 5MG $501.34 Buy

Agalsidase Beta Chemical Properties,Uses,Production

Description

Fabry's disease is a rare genetic glycolipid-storage disorder characterized by the deficiency of the lysosomal enzyme a-galactosidase A. This enzyme participates in the catabolism of the glycosphingolipid globotriaosylceramide (Gb3) by specifically cleaving its terminal s-linked galactose residue. Progressive accumulation of Gb3 and related glycosphingolipids in vascular endothelial lysosomes of the kidneys, heart, skin and brain leads to several chronic symptoms such as debilitating neuropathic pain and characteristic cutaneous lesions called angiokeratomas. As vital organs are affected with age, premature death usually occurs in the fourth or fifth decade of life due to renal, cardiac or cerebral complications. Agalsidase alfa is delivered to its lysosomal site of action via the recognition of its mannose-6-phosphate (M6P) residues by specific M6P receptors on the cell surface followed by endocytosis. In clinical trials, twice weekly intravenous infusions of agalsidase alfa over six months to one year have been found to be safe and effective in reversing the accumulation of microvascular endothelial deposits of globotriaosylceramide in the kidneys, heart and skin.

Originator

Transkaryotic Therapies (US)

Uses

Treatment of Fabry Disease.

Definition

ChEBI: Eliglustat tartrate is a tartrate that is the hemitartrate salt of eliglustat. A ceramide glucosyltransferase inhibitor used (as its tartrate salt) for treatment of Gaucher's disease. It has a role as an EC 2.4.1.80 (ceramide glucosyltransferase) inhibitor. It contains an eliglustat(1+).

brand name

Replagal (Transkaryotic Therapies).

Clinical Use

Treatment of Fabry disease. Only to be prescribed by specialist centres.

Drug interactions

Potentially hazardous interactions with other drugs
Fabrazyme should not be administered with chloroquine, amiodarone, benoquin or gentamicin due to a theoretical risk of inhibition of intra-cellular α-galactosidase activity.

Metabolism

Metabolic degradation pathway similar to other proteins.

Agalsidase Beta Preparation Products And Raw materials

Raw materials

Preparation Products

Agalsidase Beta Suppliers

Global( 2)Suppliers
Supplier Tel Email Country ProdList Advantage
Beijing HuaMeiHuLiBiological Chemical 010-56205725 waley188@sohu.com China 12338 58
AntibodySystem 17762345272 18162686757 biolab-reagents@atagenix.com China 9809 58
Agalsidase Beta Research Grade Fabrazyme/Agalsidase Alfa (DHC19529) 104138-64-9