Drug intelligence / Profile preview

dibenzyl trisulphide

Development stage
Phase 1
Lead developer
Loma Linda University Health
Modality
Small Molecules
Administration
Oral
01

Overview

Dibenzyl trisulphide (DTS) is a naturally occurring organosulfur compound isolated primarily from the plant *Petiveria alliacea* (commonly known as guinea hen weed or anamu). It has demonstrated potent anti-proliferative and cytotoxic activity against a wide range of cancer cell lines, including non-small cell lung cancer, breast, pancreatic, and prostate cancers. Mechanistically, DTS acts as a selective small-molecule kinase inhibitor—most notably inhibiting the C-terminal kinase domain of Ribosomal S6 kinase 1—and modulates key signaling pathways such as mitogen-activated protein kinases ERK1/2 (MAPK/ERK pathway), leading to hyper-phosphorylation events critical for cell proliferation and neuronal growth[1][5][6]. DTS also inhibits the Janus kinase/signal transducer and activator of transcription 3 pathway in cancer cells[8], induces apoptosis by upregulating pro-apoptotic genes like Bax while downregulating anti-apoptotic genes like Bcl-2[8], and causes disassembly of microtubules resulting in anti-mitotic effects[7]. Additionally, it competitively inhibits Cytochrome P450 1A1 enzyme activity with potential chemopreventive properties[3]. Immunomodulatory effects include cytokine switching—downregulating pro-inflammatory Th1 cytokines while upregulating Th2 cytokines—and stimulation of reticuloendothelial system parameters such as granulocyte counts and thymic mass[6]. While not currently approved for pharmaceutical use or marketed under any brand name, DTS is under investigation for its broad anticancer potential.

Other names
DTSdibenzyl trisulfide
02

Targets

CYP1A1 (Cytochrome P450 1A1)RPS6KB1 (Ribosomal protein S6 kinase beta-1)

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