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Updated: Jul 15, 2026

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Published on: June 23, 2019
6-Substituted pyrrolo[3,4-c]pyrazoles: an improved class of CDK2 inhibitors
Maria Gabriella Brasca1, Clara Albanese, Raffaella Amici
1Oncology Business Unit, Department of Chemistry, Nerviano Medical Sciences, Viale Pasteur 10, 20014 Nerviano MI, Italy. gabriella.brasca@nervianoms.com
Abstract:
We have recently reported a new class of CDK2/cyclin A inhibitors based on a bicyclic tetrahydropyrrolo[3,4-c]pyrazole scaffold. The introduction of small alkyl or cycloalkyl groups in position 6 of this scaffold allowed variation at the other two diversity points. Conventional and polymer-assisted solution phase chemistry provided a way of generating compounds with improved biochemical and cellular activity. Optimization of the physical properties and pharmacokinetic profile led to a compound which exhibited good efficacy in vivo on A2780 human ovarian carcinoma.
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