Journals / Organic Communications / 2022 / Cilt: 15 - Sayı: 2

Design, synthesis, in silico and biological evaluation of biotinpyrazole derivatives as cytotoxic agent Rahul

Pages
117–128
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Among target agents, 3a had a considerable activity against human brain cancer cell line U251 (IC50 3.5 μM). 3a could be a promising candidate for the development of new drugs to treat tumours, particularly for brain cancer.

📌 3 Key Takeaways

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Objective & Hypothesis:Modified biotin derivatives are effective in killing cancer.
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Key Findings & Data:Herein we describe the design and synthesis of conjugated biotin-pyrazole derivatives 3a-3h to evaluate as potential anticancer agents.
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Conclusion & Impact:Among target agents, 3a had a considerable activity against human brain cancer cell line U251 (IC50 3.5 μM). 3a could be a promising candidate for the development of new drugs to treat tumours, particularly for brain cancer.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Modified biotin derivatives are effective in killing cancer. Herein we describe the design and synthesis of conjugated biotin-pyrazole derivatives 3a-3h to evaluate as potential anticancer agents. A set of compounds has been prepared by palladium catalysed aminocarbonylation using carbon monoxide in an autoclave. They were well characterized by various spectroscopic techniques and screened for anticancer activity. A cell viability assay (MTT assay) was performed on U251, A549, and HepG2 cell lines and determined their IC50 value. Among target agents, 3a had a considerable activity against human brain cancer cell line U251 (IC50 3.5 μM). 3a could be a promising candidate for the development of new drugs to treat tumours, particularly for brain cancer.

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Cite This Article

RAYANİ, R., SONİ, J. Y., PARMAR, D. R., KUSURKAR, R. V., VALA, A., ZUNJAR, V., BATTULA, S. (2022). Design, synthesis, in silico and biological evaluation of biotinpyrazole derivatives as cytotoxic agent Rahul. Organic Communications, Cilt: 15 - Sayı: 2, 117–128. https://ajindex.com/articles/417557

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