BGT-002 (326E) is an orally active dual ACLY inhibitor and PPARalpha agonist. BGT-002 reduces lipogenesis by inhibiting synthesis and promoting efflux. BGT-002 demonstrates efficacy in ameliorating metabolic dysfunction-associated steatohepatitis (MASH) and improving hyperlipidemia in vivo. BGT-002 can be used for hypercholesterolemia and MASH research[1][2][3].
Molekulargewicht:
326.47
Reinheit:
99.35
CAS Nummer:
[2127387-94-2]
Formel:
C19H34O4
Target-Kategorie:
ATP Citrate Lyase,PPAR
Anwendungsbeschreibung:
MCE Product type: Reference compound
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