Synthesis and evaluation of anticancer activity of 6-pyrazolinylcoumarin derivatives

A series of novel 6-pyrazolinylcoumarins has been synthesized via multi-step protocol. The synthetic procedure was based on the acetylation of hydroxycoumarins; Fries rearrangement and Claisen–Schmidt condensation; the target 6-[5-aryl-4,5-dihydropyrazol-3-yl]-5-hydroxy-7-methylcoumarins (33–49) wer...

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Main Authors: Yana Garazd, Myroslav Garazd, Roman Lesyk
Format: Article
Language:English
Published: Elsevier 2017-02-01
Series:Saudi Pharmaceutical Journal
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1319016416300330
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spelling doaj-76844607550a4981b9f7b67773e14eda2020-11-24T23:01:12ZengElsevierSaudi Pharmaceutical Journal1319-01642017-02-0125221422310.1016/j.jsps.2016.05.005Synthesis and evaluation of anticancer activity of 6-pyrazolinylcoumarin derivativesYana Garazd0Myroslav Garazd1Roman Lesyk2Eximed, Kharkivske shose 50, Kyiv 02160, UkraineEximed, Kharkivske shose 50, Kyiv 02160, UkraineDepartment of Pharmaceutical, Organic and Bioorganic Chemistry, Danylo Halytsky Lviv National Medical University, Pekarska 69, Lviv 79010, UkraineA series of novel 6-pyrazolinylcoumarins has been synthesized via multi-step protocol. The synthetic procedure was based on the acetylation of hydroxycoumarins; Fries rearrangement and Claisen–Schmidt condensation; the target 6-[5-aryl-4,5-dihydropyrazol-3-yl]-5-hydroxy-7-methylcoumarins (33–49) were obtained under reactions of hydrazine and 2-aryl-5-methyl-2,3-dihydropyrano[2,3-f]chromen-4,8-diones as the last phase of the protocol. Anticancer activity screening in NCI60-cell lines assay allowed identification of compound 47 with the highest level of antimitotic activity with mean GI50 value of 10.20 μM and certain sensitivity profile toward the Leukemia cell lines CCRF-CEM and MOLT-4 (GI50/TGI values 1.88/5.06 μM and 1.92/4.04 μM respectively).http://www.sciencedirect.com/science/article/pii/S1319016416300330CoumarinsPyronoflavanonesPyrazolinesAnticancer activity
collection DOAJ
language English
format Article
sources DOAJ
author Yana Garazd
Myroslav Garazd
Roman Lesyk
spellingShingle Yana Garazd
Myroslav Garazd
Roman Lesyk
Synthesis and evaluation of anticancer activity of 6-pyrazolinylcoumarin derivatives
Saudi Pharmaceutical Journal
Coumarins
Pyronoflavanones
Pyrazolines
Anticancer activity
author_facet Yana Garazd
Myroslav Garazd
Roman Lesyk
author_sort Yana Garazd
title Synthesis and evaluation of anticancer activity of 6-pyrazolinylcoumarin derivatives
title_short Synthesis and evaluation of anticancer activity of 6-pyrazolinylcoumarin derivatives
title_full Synthesis and evaluation of anticancer activity of 6-pyrazolinylcoumarin derivatives
title_fullStr Synthesis and evaluation of anticancer activity of 6-pyrazolinylcoumarin derivatives
title_full_unstemmed Synthesis and evaluation of anticancer activity of 6-pyrazolinylcoumarin derivatives
title_sort synthesis and evaluation of anticancer activity of 6-pyrazolinylcoumarin derivatives
publisher Elsevier
series Saudi Pharmaceutical Journal
issn 1319-0164
publishDate 2017-02-01
description A series of novel 6-pyrazolinylcoumarins has been synthesized via multi-step protocol. The synthetic procedure was based on the acetylation of hydroxycoumarins; Fries rearrangement and Claisen–Schmidt condensation; the target 6-[5-aryl-4,5-dihydropyrazol-3-yl]-5-hydroxy-7-methylcoumarins (33–49) were obtained under reactions of hydrazine and 2-aryl-5-methyl-2,3-dihydropyrano[2,3-f]chromen-4,8-diones as the last phase of the protocol. Anticancer activity screening in NCI60-cell lines assay allowed identification of compound 47 with the highest level of antimitotic activity with mean GI50 value of 10.20 μM and certain sensitivity profile toward the Leukemia cell lines CCRF-CEM and MOLT-4 (GI50/TGI values 1.88/5.06 μM and 1.92/4.04 μM respectively).
topic Coumarins
Pyronoflavanones
Pyrazolines
Anticancer activity
url http://www.sciencedirect.com/science/article/pii/S1319016416300330
work_keys_str_mv AT yanagarazd synthesisandevaluationofanticanceractivityof6pyrazolinylcoumarinderivatives
AT myroslavgarazd synthesisandevaluationofanticanceractivityof6pyrazolinylcoumarinderivatives
AT romanlesyk synthesisandevaluationofanticanceractivityof6pyrazolinylcoumarinderivatives
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