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Investigation of the Click-Chemical Space for Drug Design Using ZINClick.
Massarotti, Alberto.
Afiliación
  • Massarotti A; Dipartimento di Scienze del Farmaco, Università degli Studi del Piemonte Orientale "A. Avogadro", Novara, Italy. alberto.massarotti@uniupo.it.
Methods Mol Biol ; 2266: 3-10, 2021.
Article en En | MEDLINE | ID: mdl-33759118
ABSTRACT
This chapter provides a brief overview of the applications of ZINClick virtual library. In the last years, we have investigated the click-chemical space covered by molecules containing the triazole ring and generated a database of 1,2,3-triazoles called ZINClick, starting from literature reported alkynes and azides synthesizable in no more than three synthetic steps from commercially available products. This combinatorial database contains millions of 1,4-disubstituted 1,2,3-triazoles that are easily synthesizable. The library is regularly updated and can be freely downloaded from http//www.ZINClick.org . This virtual library is a good starting point to explore a new portion of chemical space.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Triazoles / Descubrimiento de Drogas / Química Clic Idioma: En Revista: Methods Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2021 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Triazoles / Descubrimiento de Drogas / Química Clic Idioma: En Revista: Methods Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2021 Tipo del documento: Article País de afiliación: Italia