Drug intelligence / Profile preview

4-farnesyloxycoumarin

Development stage
Preclinical
Modality
Small Molecules
01

Overview

4-farnesyloxycoumarin is a **natural coumarin derivative** characterized by a farnesyl group at the 4-position of the coumarin core. Isolated primarily from Apiaceae and Rutaceae plants, it demonstrates multiple pharmacological activities. Recent studies highlight its **antitumor potential**, particularly as a **pro-apoptotic and anti-proliferative agent against cancer cells**. Mechanistically, it induces apoptosis via upregulation of caspase 3, p21, and p53, and may interfere with key oncogenic proteins including **GTPase KRas, Focal Adhesion Kinase 1, and Snail1**. It also displays **antioxidant properties** through free radical scavenging. 4-farnesyloxycoumarin’s main pharmaceutical challenge is low bioavailability, and current research focuses on nanoparticle and liposomal drug delivery systems to enhance its antitumor efficacy, especially against pancreatic, breast, and prostate cancer cells[1][3].

Other names
4-farnesyloxycoumarin4-FOC4-FLC
02

Targets

FAK (Focal adhesion kinase)15-LOX (Lysyl Oxidase)KRAS (Kirsten rat sarcoma viral oncogene homolog)SNAI1 (Snail family transcriptional repressor 1)PqsR (Pseudomonas quinolone signal receptor)

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