Drug intelligence / Profile preview

S-p-bromobenzylglutathione cyclopentyl diester

Development stage
Unknown
Modality
Small Molecules
Administration
Intraperitoneal
01

Overview

S-p-bromobenzylglutathione cyclopentyl diester (BBGC, also known as BrBzGCp2) is a cell-permeable, selective small molecule inhibitor of glyoxalase 1 (GLO1). GLO1 is a rate-limiting enzyme in the glyoxalase system responsible for detoxifying methylglyoxal (MG), a reactive dicarbonyl byproduct of glycolysis. By inhibiting GLO1, BBGC induces the accumulation of cytotoxic methylglyoxal, leading to dicarbonyl stress, activation of stress-activated protein kinases (such as JNK1 and p38 MAPK), and subsequent apoptosis. BBGC has been widely utilized as a preclinical research tool to investigate the role of GLO1 and methylglyoxal in cancer biology, neurobiology (including anxiety and epilepsy), and metabolic diseases such as diabetes.

Other names
S-4-bromobenzylglutathione cyclopentyl diesterS4-bromobenzylglutathione cyclopentyl diesterS 4-bromobenzylglutathione cyclopentyl diesterS-p-bromobenzyl-glutathione cyclopentyl diester
02

Targets

GLO1 (Glyoxalase 1)MAPK14 (p38 mitogen-activated protein kinase alpha)JNK (Mitogen-activated protein kinase kinase kinase family)

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