Using Cyclic Ketones to Synthesize New 3,5,6,7,8,9-Hexahydropyrazolo[ 1,5-a]quinoline Derivatives with Antiproliferative Activities: Morphological Studies

The inhibition assays of the tested compounds demonstrated significant activity against c-Met enzymatic activity, with IC<sub>50</sub> values ranging from 0.25 to 10.30 nM. Additionally, potent inhibition was observed in the prostate PC-3 cell line, with IC<sub>50</sub> values ranging from 0.19 to 8.62 μM. These promising results highlight the potential of these compounds and encourage further research to explore their therapeutic applications in the future.

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Publication Details

Journal
Current Cancer Drug Targets
Published
2025-03-04
DOI
https://doi.org/10.2174/0115680096356497250210064209
Primary Topic
Synthesis and biological activity
Type
article
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article

Using Cyclic Ketones to Synthesize New 3,5,6,7,8,9-Hexahydropyrazolo[ 1,5-a]quinoline Derivatives with Antiproliferative Activities: Morphological Studies

Nadia Y. Megally Abdo, Marwa S. Gamaan, Rafat M. Mohareb, Ibram Refat Mikhail
Current Cancer Drug Targets
Synthesis and biological activity
article

Using Cyclic Ketones to Synthesize New 3,5,6,7,8,9-Hexahydropyrazolo[ 1,5-a]quinoline Derivatives with Antiproliferative Activities: Morphological Studies

Nadia Y. Megally Abdo, Marwa S. Gamaan, Rafat M. Mohareb, Ibram Refat Mikhail
article en

Abstract

The inhibition assays of the tested compounds demonstrated significant activity against c-Met enzymatic activity, with IC<sub>50</sub> values ranging from 0.25 to 10.30 nM. Additionally, potent inhibition was observed in the prostate PC-3 cell line, with IC<sub>50</sub> values ranging from 0.19 to 8.62 μM. These promising results highlight the potential of these compounds and encourage further research to explore their therapeutic applications in the future.

Current Cancer Drug TargetsVol. 26(1)
Prince Sattam Bin Abdulaziz University (SA), Cairo University (EG), Alexandria University (EG)
Good health and well-being
Openalex Percentile: Top 97%
Synthesis and biological activity
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