Date published: 2026-4-24

1-800-457-3801

SCBT Portrait Logo
Seach Input

Trehalase Inhibitors

Trehalase inhibitors are a category of chemical compounds that interact with the enzyme trehalase, which is responsible for the hydrolysis of trehalose, a disaccharide sugar consisting of two glucose molecules. Trehalose is prevalent in many organisms, including bacteria, fungi, plants, invertebrates, and some vertebrates, serving as an energy source and stress protectant. The enzyme trehalase catalyzes the conversion of trehalose to glucose, thus facilitating the utilization of trehalose as an energy source. Inhibitors of trehalase are designed to obstruct this enzymatic action, thereby affecting the breakdown of trehalose within cells. By binding to the active site or another critical region of the trehalase enzyme, these inhibitors impede the proper interaction between the enzyme and its substrate, trehalose, modulating the biochemical pathways that rely on this sugar for energy and protection. The structural diversity of trehalase inhibitors is significant, reflecting the complexity of enzyme-inhibitor interactions and the varying contexts in which trehalase operates. These inhibitors may be found in different chemical classes, with some mimicking the structure of trehalose to compete with it for the enzyme's active site, while others are designed based on the enzyme's other functional domains. The mechanism by which these inhibitors function may involve reversible or irreversible binding to trehalase, with some forming a temporary interaction that can be displaced by an excess of substrate, and others forming a permanent bond, effectively inactivating the enzyme.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Validamycin A

37248-47-8sc-281183
sc-281183A
sc-281183B
sc-281183C
1 g
5 g
10 g
25 g
$156.00
$298.00
$544.00
$738.00
2
(1)

Validamycin A functions as a trehalase, exhibiting a unique ability to hydrolyze trehalose into glucose units. Its specific binding affinity for trehalose enhances substrate recognition, leading to efficient catalytic activity. The compound's structural features facilitate the stabilization of transition states, optimizing reaction kinetics. Furthermore, Validamycin A's selectivity for trehalose over other disaccharides underscores its distinct role in carbohydrate metabolism, influencing energy release and cellular processes.

Castanospermine

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

An indolizidine alkaloid that inhibits trehalase by acting as a competitive inhibitor.

Deoxynojirimycin

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

An iminosugar that inhibits trehalase by mimicking the transition state of the hydrolysis reaction.

Miglitol

72432-03-2sc-221943
10 mg
$161.00
1
(1)

A pseudo-tetrasaccharide that inhibits trehalase by competitive inhibition.

Voglibose

83480-29-9sc-204384
sc-204384A
10 mg
50 mg
$198.00
$681.00
(1)

An oligosaccharide that inhibits trehalase by occupying the active site of the enzyme.

Acarbose

56180-94-0sc-203492
sc-203492A
1 g
5 g
$226.00
$605.00
1
(1)

A pseudo-tetrasaccharide that inhibits trehalase by competitively inhibiting the enzyme.

1,6-Anhydro-β-D-glucopyranose

498-07-7sc-220561
sc-220561A
sc-220561B
sc-220561C
2 g
5 g
25 g
100 g
$141.00
$270.00
$255.00
$525.00
(0)

A pyrrolidine derivative that inhibits trehalase by mimicking the transition state of its substrate.