Drug intelligence / Profile preview

SelSA-1

Development stage
Preclinical
Modality
Small Molecules
Administration
Intraperitoneal
01

Overview

SelSA-1 is a **selenium-containing derivative of SAHA (suberoylanilide hydroxamic acid)** that functions as an **HDAC (histone deacetylase) inhibitor** with enhanced chemotherapeutic properties. The compound was designed by incorporating selenium into the SAHA molecule structure to combine the epigenetic regulatory capabilities of HDAC inhibition with the anti-tumorigenic properties of selenium. SelSA-1 demonstrates **improved efficacy and safety profiles compared to its parent compound SAHA**, showing lower IC50 values in cancer cell lines while maintaining better safety margins in normal cells. The compound exerts its anti-cancer effects through **redox modulation of multiple epigenetic and apoptotic pathways**, inducing oxidative stress in cancer cells while promoting resolution of inflammation. SelSA-1 has been primarily studied in preclinical models of **colorectal cancer**, particularly in colitis-associated cancer (CAC) models, where it demonstrated superior reduction in tumor burden, incidence, and inflammatory markers compared to SAHA.

Other names
Selenium analog of SAHA
02

Targets

HDAC10 (Histone Deacetylase 10)HDAC6 (Histone deacetylase 6)

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