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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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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1725640398394621952 |