Date published: 2025-11-22

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KAT II Inhibitors

KAT II inhibitors, also known as Kynurenine aminotransferase II inhibitors, belong to a specific class of compounds that target enzymes involved in the kynurenine pathway, a critical metabolic route for tryptophan degradation. The kynurenine pathway plays a pivotal role in the metabolism of tryptophan, an essential amino acid, and its dysregulation has been implicated in various neurological and inflammatory disorders. KAT II, one of the key enzymes in this pathway, catalyzes the conversion of kynurenine to kynurenic acid, a metabolite that can modulate glutamatergic neurotransmission.The chemical structure of KAT II inhibitors is characterized by their ability to selectively bind and inhibit the activity of the Kynurenine aminotransferase II enzyme. These compounds typically feature specific functional groups and molecular motifs that interact with the active site of KAT II, disrupting its catalytic function. By modulating the enzymatic activity of KAT II, these inhibitors have the potential to influence the balance of metabolites in the kynurenine pathway, leading to downstream effects on neurotransmitter systems and cellular processes.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

(S)-ESBA hydrochloride

sc-222282
sc-222282A
1 mg
5 mg
$58.00
$170.00
1
(0)

(S)-ESBA hydrochloride exhibits distinctive reactivity as an acid halide, characterized by its ability to form stable acyl derivatives through nucleophilic acyl substitution. Its chiral nature influences stereoselectivity in reactions, allowing for the formation of enantiomerically enriched products. The compound's strong electrophilic character enhances its reactivity with amines and alcohols, facilitating rapid esterification and amidation processes. Additionally, its solubility in organic solvents supports diverse synthetic applications.

(S)-2-(4-(4-Chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl)-N-(4-hydroxyphenyl)acetamide

202590-98-5sc-501130
2.5 mg
$330.00
(0)

BFF-816 is an irreversible inhibitor of KAT II that forms a covalent bond with the active site of the enzyme.

Zinc

7440-66-6sc-213177
100 g
$47.00
(0)

ZINC58496327 inhibits KAT II by binding to the enzyme's active site and preventing substrate binding.

A 922500

959122-11-3sc-203793
10 mg
$265.00
2
(1)

A-922500 is a potent, bioavailable, and selective inhibitor of KAT II. It inhibits KAT II by binding to the active site of the enzyme.