Signal transducer and activator of transcription 3 (STAT3) is a protein constitutively activated by aberrant upstream tyrosine kinase activities in a broad spectrum of human solid and blood tumors. Therefore, the availability of drugs affecting STAT3 may have important therapeutic potential for the treatment of cancer. Pursuing our efforts in exploring the influence of the substitution pattern of the ureido 1,2,5-oxadiazole moiety on the molecular conformation, new compounds substituted at positions 3 and 4 on the furazane ring were synthesized. The inhibition properties vs. STAT3 of the novel compounds were evaluated in a dual-luciferase assay, using HCT-116 cells, and the results evidenced a moderate activity only for the compounds endowed with a planar arrangement. Crystallographic studies of the new derivatives were performed in order to evidence the peculiar chemical behavior and to evaluate how structural modulations affected the biological properties. Copyright

The influence of the substitution pattern on the molecular conformation of ureido 1,2,5-oxadiazoles, related to STAT3 inhibitors: chemical behavior and structural investigation / S. Villa, D. Masciocchi, A. Gelain, F. Meneghetti. - In: CHEMISTRY & BIODIVERSITY. - ISSN 1612-1872. - 9:7(2012), pp. 1240-1253.

The influence of the substitution pattern on the molecular conformation of ureido 1,2,5-oxadiazoles, related to STAT3 inhibitors: chemical behavior and structural investigation

S. Villa
Primo
;
D. Masciocchi
Secondo
;
A. Gelain
Penultimo
;
F. Meneghetti
Ultimo
2012

Abstract

Signal transducer and activator of transcription 3 (STAT3) is a protein constitutively activated by aberrant upstream tyrosine kinase activities in a broad spectrum of human solid and blood tumors. Therefore, the availability of drugs affecting STAT3 may have important therapeutic potential for the treatment of cancer. Pursuing our efforts in exploring the influence of the substitution pattern of the ureido 1,2,5-oxadiazole moiety on the molecular conformation, new compounds substituted at positions 3 and 4 on the furazane ring were synthesized. The inhibition properties vs. STAT3 of the novel compounds were evaluated in a dual-luciferase assay, using HCT-116 cells, and the results evidenced a moderate activity only for the compounds endowed with a planar arrangement. Crystallographic studies of the new derivatives were performed in order to evidence the peculiar chemical behavior and to evaluate how structural modulations affected the biological properties. Copyright
1,2,5-Oxadiazoles, ureido-; Inhibitors; Signal transducer and activator of transcription 3 (STAT3); Structure-activity relationship (SAR); X-Ray crystallography
Settore CHIM/08 - Chimica Farmaceutica
2012
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/212651
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