Drug intelligence / Profile preview

carabrone

Development stage
Preclinical
Lead developer
Nanjing Drum-Tower Hospital
Modality
Small Molecules
Administration
Oral, Intraperitoneal
01

Overview

Carabrone is a natural sesquiterpene lactone isolated from the traditional Chinese herb *Carpesium abrotanoides* L. and other *Carpesium* species. It is being investigated as a preclinical therapeutic candidate for various inflammatory, metabolic, and neurodegenerative disorders. Carabrone acts as a multi-target inhibitor, directly binding to the NACHT domain of the NLR family pyrin domain-containing 3 (NLRP3) inflammasome to prevent its activation and assembly. Additionally, it directly binds to and inhibits signal transducer and activator of transcription 3 (STAT3) activation, and covalently targets ubiquitin-conjugating enzyme E2 D3 (UBE2D3) at the cysteine 85 residue to suppress NF-κB signaling. Through these mechanisms, carabrone has demonstrated therapeutic efficacy in animal models of Alzheimer's disease, multiple sclerosis, metabolic dysfunction-associated steatohepatitis (MASH), gouty arthritis, sepsis, and pancreatic cancer.

Other names
(3aR,4aS,5S,5aR,6aR)-5a-methyl-3-methylidene-5-(3-oxobutyl)octahydro-2H-cyclopropa[f][1]benzofuran-2-oneCAOctahydro-5a-methyl-3-methylene-5-(3-oxobutyl)-2H-cyclopropa[f]benzofuran-2-one
02

Targets

NLRP3 (Nod-like receptor family pyrin domain-containing protein 3)STAT3 (Signal Transducer and Activator of Transcription 3)UBE2D3 (Ubiquitin-conjugating enzyme E2 D3)

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