Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Compound 6q is an experimental small molecule tubulin inhibitor belonging to a series of 1-phenyl-3-(2-phenylpyridin-3-yl)urea congeners. Designed as a structural analog of the anti-cancer agent E7010 (ER-86526), it demonstrates potent anti-proliferative activity against various human cancer cell lines, including prostate (DU-145), lung (A549), cervical (HeLa), and breast (MDA-MB-231) cancers, with IC50 values ranging from 2.03 to 8.14 µM. Mechanistically, compound 6q binds to the colchicine binding site of β-tubulin, disrupting microtubule dynamics and arresting the cell cycle at the G2/M phase. This disruption triggers apoptosis through both nuclear and mitochondrial pathways and has been shown to inhibit cancer cell migration.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on compound 6q.