Drug intelligence / Profile preview

dihydrocucurbitacin b

Development stage
Preclinical
Modality
Small Molecules
Administration
Intraperitoneal, Oral
01

Overview

Dihydrocucurbitacin B is a naturally occurring cucurbitane triterpenoid isolated from various plants of the Cucurbitaceae family, including *Cayaponia tayuya*, *Wilbrandia ebracteata*, and *Trichosanthes kirilowii*. It exhibits a wide range of pharmacological activities, including anti-inflammatory, immunosuppressive, lipid-lowering, and anticancer properties. Mechanistically, dihydrocucurbitacin B has been shown to selectively inhibit the nuclear factor of activated T cells (NFAT) in human lymphocytes and suppress cyclooxygenase-2 (COX-2) activity. In lipid metabolism, it promotes LDL clearance by upregulating low-density lipoprotein receptor (LDLR) expression and downregulating proprotein convertase subtilisin/kexin type 9 (PCSK9) expression. In oncology models, it induces G2/M cell-cycle arrest and apoptosis, potentially through the downregulation of the PI3K/Akt/mTOR signaling pathway and cyclins such as cyclin B1.

Other names
23,24-dihydrocucurbitacin BDHCBdihydrocucurbitacin B
02

Targets

PTGS2 (Prostaglandin-Endoperoxide Synthase 2)HNF1A (Hepatocyte nuclear factor 1-alpha)LDLR (Low-density lipoprotein receptor)NFAT (NFAT family)PCSK9 (Proprotein convertase subtilisin/kexin type 9)SREBP-2 / SREBF2 (SREBP-2)

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