Identification and Biological Characterization of the Pyrazolo[3,4-<i>d</i>]pyrimidine Derivative SI388 Active as Src Inhibitor

Src is a non-receptor tyrosine kinase (TK) whose involvement in cancer, including glioblastoma (GBM), has been extensively demonstrated. In this context, we started from our <i>in-house</i> library of pyrazolo[3,4-<i>d</i>]pyrimidines that are active as Src and/or Bcr-Abl TK...

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Hoofdauteurs: Claudia Contadini (Auteur), Claudia Cirotti (Auteur), Anna Carbone (Auteur), Mehrdad Norouzi (Auteur), Annarita Cianciusi (Auteur), Emmanuele Crespan (Auteur), Cecilia Perini (Auteur), Giovanni Maga (Auteur), Daniela Barilà (Auteur), Francesca Musumeci (Auteur), Silvia Schenone (Auteur)
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Gepubliceerd in: MDPI AG, 2023-07-01T00:00:00Z.
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100 1 0 |a Claudia Contadini  |e author 
700 1 0 |a Claudia Cirotti  |e author 
700 1 0 |a Anna Carbone  |e author 
700 1 0 |a Mehrdad Norouzi  |e author 
700 1 0 |a Annarita Cianciusi  |e author 
700 1 0 |a Emmanuele Crespan  |e author 
700 1 0 |a Cecilia Perini  |e author 
700 1 0 |a Giovanni Maga  |e author 
700 1 0 |a Daniela Barilà  |e author 
700 1 0 |a Francesca Musumeci  |e author 
700 1 0 |a Silvia Schenone  |e author 
245 0 0 |a Identification and Biological Characterization of the Pyrazolo[3,4-<i>d</i>]pyrimidine Derivative SI388 Active as Src Inhibitor 
260 |b MDPI AG,   |c 2023-07-01T00:00:00Z. 
500 |a 10.3390/ph16070958 
500 |a 1424-8247 
520 |a Src is a non-receptor tyrosine kinase (TK) whose involvement in cancer, including glioblastoma (GBM), has been extensively demonstrated. In this context, we started from our <i>in-house</i> library of pyrazolo[3,4-<i>d</i>]pyrimidines that are active as Src and/or Bcr-Abl TK inhibitors and performed a lead optimization study to discover a new generation derivative that is suitable for Src kinase targeting. We synthesized a library of 19 compounds, <b>2a-s</b>. Among these, compound <b>2a</b> (SI388) was identified as the most potent Src inhibitor. Based on the cell-free results, we investigated the effect of SI388 in 2D and 3D GBM cellular models. Interestingly, SI388 significantly inhibits Src kinase, and therefore affects cell viability, tumorigenicity and enhances cancer cell sensitivity to ionizing radiation. 
546 |a EN 
690 |a Src kinase 
690 |a glioblastoma 
690 |a radiotherapy resistance 
690 |a pyrazolo[3,4-<i>d</i>]pyrimidines 
690 |a Medicine 
690 |a R 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceuticals, Vol 16, Iss 7, p 958 (2023) 
787 0 |n https://www.mdpi.com/1424-8247/16/7/958 
787 0 |n https://doaj.org/toc/1424-8247 
856 4 1 |u https://doaj.org/article/cb6c5b3f3a3c4429a456fa6d37613bc6  |z Connect to this object online.