Date published: 2026-5-9

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MAN1A2 Inhibitors

MAN1A2 inhibitors are a class of chemical compounds that specifically target and inhibit the enzyme alpha-mannosidase 1A2 (MAN1A2), which is a glycosyl hydrolase involved in the processing of N-linked glycans in the Golgi apparatus. MAN1A2 plays a crucial role in the trimming of mannose residues from glycoproteins during their maturation and trafficking through the secretory pathway. The inhibition of MAN1A2 disrupts this glycosylation process, leading to alterations in the structure and function of glycoproteins. This, in turn, can affect various cellular processes, including protein folding, stability, and transport, as glycosylation is essential for the proper functioning and localization of many proteins within the cell.Structurally, MAN1A2 inhibitors can be diverse, often incorporating functional groups that interact with the active site of the enzyme to prevent its catalytic activity. These inhibitors may mimic the natural substrates of MAN1A2, binding to the enzyme in a competitive manner, or they may interact with other critical regions of the enzyme to exert an allosteric effect. The development of MAN1A2 inhibitors often involves extensive studies on the enzyme's structure to identify key binding sites and to optimize the affinity and specificity of the inhibitor. Inhibition of MAN1A2 has significant implications for the glycosylation pathways, and the detailed study of these inhibitors provides insights into the broader aspects of glycan processing and protein modification. Researchers continue to explore the biochemical interactions and consequences of MAN1A2 inhibition to better understand the enzyme's role in cellular homeostasis and its broader impact on glycoprotein biology.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Kifunensine

109944-15-2sc-201364
sc-201364A
sc-201364B
sc-201364C
1 mg
5 mg
10 mg
100 mg
$135.00
$540.00
$1025.00
$6248.00
25
(2)

Kifunensine acts as a selective inhibitor of the MAN1A2 enzyme, exhibiting unique molecular interactions that disrupt glycan maturation. Its specific binding affinity to the enzyme's active site alters the conformational dynamics, leading to a significant reduction in mannose trimming efficiency. This compound's distinct stereochemical arrangement influences the reaction kinetics, resulting in a pronounced effect on glycan structures and their subsequent biological implications.

Swainsonine

72741-87-8sc-201362
sc-201362C
sc-201362A
sc-201362D
sc-201362B
1 mg
2 mg
5 mg
10 mg
25 mg
$138.00
$251.00
$631.00
$815.00
$1832.00
6
(1)

Swainsonine inhibits alpha-mannosidase 2 by directly binding to its active site, preventing the enzymatic cleavage of mannose residues from glycoproteins, a key function of alpha-mannosidase 2.

Deoxymannojirimycin hydrochloride

84444-90-6sc-201360
sc-201360A
1 mg
5 mg
$93.00
$239.00
2
(0)

Deoxymannojirimycin acts as a competitive inhibitor of alpha-mannosidase 2 by mimicking the structure of mannose. It binds to the enzyme's active site, blocking the access of natural substrates.

Deoxynojirimycin

19130-96-2sc-201369
sc-201369A
1 mg
5 mg
$73.00
$145.00
(0)

1-Deoxynojirimycin competitively inhibits alpha-mannosidase 2 by resembling the structure of mannose, effectively blocking the enzyme's active site and hindering its function.

Castanospermine

79831-76-8sc-201358
sc-201358A
100 mg
500 mg
$184.00
$632.00
10
(1)

Castanospermine inhibits alpha-mannosidase 2 by binding to the enzyme's active site, thereby preventing the breakdown of mannose-containing oligosaccharides.

AM 580

102121-60-8sc-203505
sc-203505A
5 mg
25 mg
$99.00
$390.00
2
(1)

AM 580 directly inhibits alpha-mannosidase 2 by mimicking the substrate and binding to the enzyme's active site, obstructing its normal enzymatic activity.