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Design, Synthesis and Tumour-Selective Toxicity of Novel 1-[3-{3,5-Bis(benzylidene)-4-oxo-1-piperidino}-3-oxopropyl]-4-piperidone Oximes and Related Quaternary Ammonium Salts

A novel series of 1-[3-{3,5-bis(benzylidene)-4-oxo-1-piperidino}-3-oxopropyl]-4-piperidone oximes - and related quaternary ammonium salts - were prepared as candidate antineoplastic agents. Evaluation against neoplastic Ca9-22, HSC-2 and HSC-4 cells revealed the compounds in series and to be potent...

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Published in:Molecules (Basel, Switzerland) Switzerland), 2021-11, Vol.26 (23), p.7132
Main Authors: Roayapalley, Praveen K, Dimmock, Jonathan R, Contreras, Lisett, Balderrama, Karol S, Aguilera, Renato J, Sakagami, Hiroshi, Amano, Shigeru, Sharma, Rajendra K, Das, Umashankar
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cited_by cdi_FETCH-LOGICAL-c493t-1f836134c3f9532e5038900d9597cb6b46772d65154d8bcab4b27432b00c8ad03
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creator Roayapalley, Praveen K
Dimmock, Jonathan R
Contreras, Lisett
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Sakagami, Hiroshi
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Sharma, Rajendra K
Das, Umashankar
description A novel series of 1-[3-{3,5-bis(benzylidene)-4-oxo-1-piperidino}-3-oxopropyl]-4-piperidone oximes - and related quaternary ammonium salts - were prepared as candidate antineoplastic agents. Evaluation against neoplastic Ca9-22, HSC-2 and HSC-4 cells revealed the compounds in series and to be potent cytotoxins with submicromolar CC values in virtually all cases. In contrast, the compounds were less cytocidal towards HGF, HPLF and HPC non-malignant cells revealing their tumour-selective toxicity. Quantitative structure-activity relationships revealed that, in general, both cytotoxic potency and selectivity index figures increased as the magnitude of the Hammett sigma values rose. In addition, - are cytotoxic towards a number of leukemic and colon cancer cells. , lowered the mitochondrial membrane potential in CEM cells, and induced transient G2/M accumulation in Ca9-22 cells. Five compounds, namely , and , were identified as lead molecules that have drug-like properties.
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Evaluation against neoplastic Ca9-22, HSC-2 and HSC-4 cells revealed the compounds in series and to be potent cytotoxins with submicromolar CC values in virtually all cases. In contrast, the compounds were less cytocidal towards HGF, HPLF and HPC non-malignant cells revealing their tumour-selective toxicity. Quantitative structure-activity relationships revealed that, in general, both cytotoxic potency and selectivity index figures increased as the magnitude of the Hammett sigma values rose. In addition, - are cytotoxic towards a number of leukemic and colon cancer cells. , lowered the mitochondrial membrane potential in CEM cells, and induced transient G2/M accumulation in Ca9-22 cells. 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subjects Ammonium
Ammonium salts
Antineoplastic Agents - chemical synthesis
Antineoplastic Agents - chemistry
Antineoplastic Agents - pharmacology
Apoptosis - drug effects
Cancer
Cell cycle
Cell Line, Tumor
Cell Proliferation - drug effects
Colon
Colon cancer
Colonic Neoplasms - drug therapy
Colorectal cancer
conjugated unsaturated ketones
Cytotoxicity
Cytotoxins
Fibroblasts
Humans
Laboratories
Leukemia
Membrane potential
Mitochondria
mitochondrial membrane potential
Nitrogen
Oximes
Oximes - chemical synthesis
Oximes - chemistry
Oximes - pharmacology
QSAR
Quantitative Structure-Activity Relationship
Quaternary Ammonium Compounds - chemical synthesis
Quaternary Ammonium Compounds - chemistry
Quaternary Ammonium Compounds - pharmacology
Quaternary ammonium salts
Salts
Selectivity
Toxicity
Tumors
title Design, Synthesis and Tumour-Selective Toxicity of Novel 1-[3-{3,5-Bis(benzylidene)-4-oxo-1-piperidino}-3-oxopropyl]-4-piperidone Oximes and Related Quaternary Ammonium Salts
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