A series of 1,2,5-oxadiazoles was synthesized as new potential antiproliferative agents. The in vitro cytotoxic activity evaluation of title compounds through MTT-assay revealed that some of them showed significant activity against the HCT-116 cancer cell line. The field-based disparity analysis provided indications about the electrostatic, hydrophobic and shape features underlying the cytotoxicity, suggesting that increasing the negative electrostatic field on the heterocyclic core of the structure has positive effects on the activity. The structure-activity relationships (SAR) around a particular compound can be explained allowing for a structural rationale for the differences in activity. The SAR provided by this series of compounds can be exploited to carry out further lead optimization.

A field-based disparity analysis of new 1,2,5-oxadiazole derivatives endowed with antiproliferative activity / F. Porta, A. Gelain, D. Barlocco, N. Ferri, S. Marchiano', V. Cappello, L. Basile, S. Guccione, F. Meneghetti, S. Villa. - In: CHEMICAL BIOLOGY & DRUG DESIGN. - ISSN 1747-0277. - 90:5(2017 Nov), pp. 820-839. [10.1111/cbdd.13003]

A field-based disparity analysis of new 1,2,5-oxadiazole derivatives endowed with antiproliferative activity

F. Porta;A. Gelain;D. Barlocco;N. Ferri;S. Marchiano';V. Cappello;F. Meneghetti
;
S. Villa
2017

Abstract

A series of 1,2,5-oxadiazoles was synthesized as new potential antiproliferative agents. The in vitro cytotoxic activity evaluation of title compounds through MTT-assay revealed that some of them showed significant activity against the HCT-116 cancer cell line. The field-based disparity analysis provided indications about the electrostatic, hydrophobic and shape features underlying the cytotoxicity, suggesting that increasing the negative electrostatic field on the heterocyclic core of the structure has positive effects on the activity. The structure-activity relationships (SAR) around a particular compound can be explained allowing for a structural rationale for the differences in activity. The SAR provided by this series of compounds can be exploited to carry out further lead optimization.
No
English
SAR; Activity cliff; Anticancer agents; Heteroaryl amide; X-ray
Settore CHIM/08 - Chimica Farmaceutica
Articolo
Esperti anonimi
Ricerca di base
Pubblicazione scientifica
nov-2017
Wiley
90
5
820
839
20
Pubblicato
Periodico con rilevanza internazionale
crossref
pubmed
Aderisco
info:eu-repo/semantics/article
A field-based disparity analysis of new 1,2,5-oxadiazole derivatives endowed with antiproliferative activity / F. Porta, A. Gelain, D. Barlocco, N. Ferri, S. Marchiano', V. Cappello, L. Basile, S. Guccione, F. Meneghetti, S. Villa. - In: CHEMICAL BIOLOGY & DRUG DESIGN. - ISSN 1747-0277. - 90:5(2017 Nov), pp. 820-839. [10.1111/cbdd.13003]
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Prodotti della ricerca::01 - Articolo su periodico
10
262
Article (author)
no
F. Porta, A. Gelain, D. Barlocco, N. Ferri, S. Marchiano', V. Cappello, L. Basile, S. Guccione, F. Meneghetti, S. Villa
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/494369
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