Date published: 2026-4-23

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SUDD Inhibitors

SUDD inhibitors, also known as suicide inhibitors or mechanism-based inhibitors, are a class of chemical compounds designed to interfere with the activity of specific enzymes within biological systems. These inhibitors are distinct in their mechanism of action, which involves forming a covalent bond with the target enzyme, rendering it permanently inactive. The term suicide inhibitor aptly describes this irreversible binding process, as the inhibitor essentially sacrifices itself in the process of deactivating the enzyme. The mechanism of action of SUDD inhibitors begins with the compound being recognized by the target enzyme, often due to its structural similarity to the enzyme's natural substrate. Once bound to the enzyme's active site, the inhibitor undergoes a chemical transformation, usually involving a reaction that generates a highly reactive intermediate or radical species. This intermediate then reacts with essential amino acid residues within the enzyme's active site, forming a stable covalent bond.

As a result of this covalent modification, the enzyme's catalytic activity is permanently disrupted. This process is akin to a chemical suicide for the inhibitor, as it becomes irreversibly bound to the enzyme and is no longer available for other reactions.SUDD inhibitors find extensive use in biochemical and pharmacological research to elucidate enzyme function and explore potential drug targets. They are invaluable tools for understanding enzyme kinetics, substrate specificity, and the role of specific enzymes in various biological pathways. Overall, SUDD inhibitors play a crucial role in advancing our understanding of enzymatic processes and have broad applications in both basic research and drug development.

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Items 1 to 10 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Aspirin

50-78-2sc-202471
sc-202471A
5 g
50 g
$20.00
$42.00
4
(1)

Irreversibly inhibits cyclooxygenase, reducing prostaglandin production and inflammation.

Omeprazole

73590-58-6sc-202265
50 mg
$67.00
4
(1)

Covalently binds to the H+/K+ ATPase pump in gastric parietal cells, reducing acid secretion in the stomach.

Warfarin

81-81-2sc-205888
sc-205888A
1 g
10 g
$73.00
$246.00
7
(1)

Interferes with vitamin K-dependent clotting factors, inhibiting blood coagulation.

Allopurinol

315-30-0sc-207272
25 g
$131.00
(0)

Inhibits xanthine oxidase, reducing the conversion of xanthine to uric acid and preventing gout attacks.

Imatinib

152459-95-5sc-267106
sc-267106A
sc-267106B
10 mg
100 mg
1 g
$26.00
$119.00
$213.00
27
(1)

Blocks the tyrosine kinase activity of BCR-ABL, inhibiting the growth of cancer cells in chronic myeloid leukemia.

Ivermectin

70288-86-7sc-203609
sc-203609A
100 mg
1 g
$57.00
$77.00
2
(2)

Binds to glutamate-gated chloride channels in parasites, leading to paralysis and death of the parasites.

Ritonavir

155213-67-5sc-208310
10 mg
$124.00
7
(1)

Inhibits HIV protease, preventing the cleavage of viral polyproteins and reducing the production of mature virions.

Donepezil

120014-06-4sc-279006
10 mg
$74.00
3
(1)

Reversibly inhibits acetylcholinesterase, increasing acetylcholine levels.

Tamoxifen

10540-29-1sc-208414
2.5 g
$272.00
18
(2)

Competes with estrogen for binding to the estrogen receptor, inhibiting the growth of estrogen-dependent breast cancer cells.

Captopril

62571-86-2sc-200566
sc-200566A
1 g
5 g
$49.00
$91.00
21
(1)

Blocks angiotensin-converting enzyme (ACE), reducing the formation of angiotensin II and lowering blood pressure.