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Novel pyrazolo[4,3-d]pyrimidine microtubule targeting agents (MTAs): Synthesis, structure–activity relationship, in vitro and in vivo evaluation as antitumor agents

The design, synthesis, and biological evaluation of a series novel N1‑methyl pyrazolo[4,3-d]pyrimidines as inhibitors of tubulin polymerization and colchicine binding were described here. Synthesis of target compounds involved alkylation of the pyrazolo scaffold, which afforded two regioisomers. The...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Bioorg Med Chem Lett
Päätekijät: Islam, Farhana, Quadery, Tasdique M., Bai, Ruoli, Luckett-Chastain, Lerin R., Hamel, Ernest, Ihnat, Michael A., Gangjee, Aleem
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2021
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC8113149/
https://ncbi.nlm.nih.gov/pubmed/33705908
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmcl.2021.127923
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