Synthesis of new bis-thiosemicarbazones based on 2,2’-[propane-1,3-diil-bis-(oxi)]dibenzaldehyde with biological potential

Cancer is the second most common cause of death. No known drug meets 100% the needs of the medical industry. For these reasons, many researchers are trying to synthesize new molecules with anti-cancer properties. A class of organic compounds called thiosemicarbazones exhibit a broad spectrum of useful biological activities including anticancer and antimicrobial. One of the possible mechanisms of the anticancer action of thiosemicarbazones is the inhibition of topoisomerase IIα. In this article the synthetic procedure of some novel bis-thiosemicarbazones is described. Their topoisomerase IIα inhibition potential was estimated by Molecular Docking method.

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Journal
Studia Universitatis Moldaviae Seria Științe ale Naturii
Published
2024-12-01
DOI
https://doi.org/10.59295/sum6(176)2024_27
Primary Topic
Synthesis and biological activity
Type
article
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article

Synthesis of new bis-thiosemicarbazones based on 2,2’-[propane-1,3-diil-bis-(oxi)]dibenzaldehyde with biological potential

Roman Rusnac, Aurélian Gulea, Andrei Ciursin
Studia Universitatis Moldaviae Seria Științe ale Naturii
Synthesis and biological activity
article

Synthesis of new bis-thiosemicarbazones based on 2,2’-[propane-1,3-diil-bis-(oxi)]dibenzaldehyde with biological potential

Roman Rusnac, Aurélian Gulea, Andrei Ciursin
article en

Abstract

Cancer is the second most common cause of death. No known drug meets 100% the needs of the medical industry. For these reasons, many researchers are trying to synthesize new molecules with anti-cancer properties. A class of organic compounds called thiosemicarbazones exhibit a broad spectrum of useful biological activities including anticancer and antimicrobial. One of the possible mechanisms of the anticancer action of thiosemicarbazones is the inhibition of topoisomerase IIα. In this article the synthetic procedure of some novel bis-thiosemicarbazones is described. Their topoisomerase IIα inhibition potential was estimated by Molecular Docking method.

Studia Universitatis Moldaviae Seria Științe ale Naturii(6 (176))
Moldova State University (MD)
Openalex Percentile: Top 81%
Synthesis and biological activity
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