Isoxazolyl(isothiazolyl)pyridyl substituted 1,2,4- and 1,3,4-oxadiazoles as potential inhibitors of HA-CD44 interaction: Synthesis and anticancer activity

Authors: Ekaterina A. Akishina, Yury V. Kornoushenko, Alexander M. Andrianov et al.
Publication: Tetrahedron
Published: Jul 1, 2026
Source: Crossref
Back to Search View Original Cite This Article

Related Articles

Sulfur- and water-tolerant vanadium-substituted phosphomolybdic acid catalysts for NH3-SCR: Combined experimental and DFT studies

Lina Guo, Qi Ding et al. - Nov 2026

Read More
Theoretical design of novel selenium-substituted meso-aryl-BODIPYs as singlet‑oxygen photosensitizers with biomedical applicability

Mónica Moral, Antonio Fernández et al. - Sep 2026

Read More
Photo- and thermal transformations of α-substituted β-ethoxyvinyl trifluoromethyl ketones

Sergey I. Vdovenko, Igor I. Gerus - Sep 2026

Read More
Investigation of in vitro photodynamic activities of PEG and glycosyl group substituted BODIPY compounds

Lamia Sevire Sekban, Ekrem Kaplan et al. - Sep 2026

Read More
Countercurrent chromatographic isolation of α′-propyl-substituted furan fatty acid ethyl esters from an eicosapentaenoic acid ethyl ester oil

Felix Rüttler, Vanessa Bauer et al. - Aug 2026

Read More