Synthesis and in vitro cytotoxicity evaluation of isatin-pyrrole derivatives against HepG2 cell line
This paper reports the synthesis and in vitro cytotoxicity evaluation of isatin-pyrrole derivatives 5–8, obtained from the appropriate isatins with pyrrole, with good yields and purity. The product structures were confirmed through spectroscopy methods. Furthermore, the MTT assay on the human liver...
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De Gruyter
2021
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oai:doaj.org-article:c1178cb56fdc4d81a52514ff1686c7d52021-12-05T14:10:43ZSynthesis and in vitro cytotoxicity evaluation of isatin-pyrrole derivatives against HepG2 cell line2391-542010.1515/chem-2021-0023https://doaj.org/article/c1178cb56fdc4d81a52514ff1686c7d52021-02-01T00:00:00Zhttps://doi.org/10.1515/chem-2021-0023https://doaj.org/toc/2391-5420This paper reports the synthesis and in vitro cytotoxicity evaluation of isatin-pyrrole derivatives 5–8, obtained from the appropriate isatins with pyrrole, with good yields and purity. The product structures were confirmed through spectroscopy methods. Furthermore, the MTT assay on the human liver cancer HepG2 cell lines revealed moderate activity in all compounds, which was highest in sample 6 (IC50 0.47 µM). The anticancer activity was affiliated with the presence of a nitro group at C-5 and N-methyl of the isatin scaffold.Santoso MardiFadlan ArifFahmi Muhammad Riza GhulamRahmayanti ArdhanaDe Gruyterarticleisatinisatin-pyrrole derivativesanticancerhepg2 cell lineChemistryQD1-999ENOpen Chemistry, Vol 19, Iss 1, Pp 199-204 (2021) |
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isatin isatin-pyrrole derivatives anticancer hepg2 cell line Chemistry QD1-999 |
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isatin isatin-pyrrole derivatives anticancer hepg2 cell line Chemistry QD1-999 Santoso Mardi Fadlan Arif Fahmi Muhammad Riza Ghulam Rahmayanti Ardhana Synthesis and in vitro cytotoxicity evaluation of isatin-pyrrole derivatives against HepG2 cell line |
description |
This paper reports the synthesis and in vitro cytotoxicity evaluation of isatin-pyrrole derivatives 5–8, obtained from the appropriate isatins with pyrrole, with good yields and purity. The product structures were confirmed through spectroscopy methods. Furthermore, the MTT assay on the human liver cancer HepG2 cell lines revealed moderate activity in all compounds, which was highest in sample 6 (IC50 0.47 µM). The anticancer activity was affiliated with the presence of a nitro group at C-5 and N-methyl of the isatin scaffold. |
format |
article |
author |
Santoso Mardi Fadlan Arif Fahmi Muhammad Riza Ghulam Rahmayanti Ardhana |
author_facet |
Santoso Mardi Fadlan Arif Fahmi Muhammad Riza Ghulam Rahmayanti Ardhana |
author_sort |
Santoso Mardi |
title |
Synthesis and in vitro cytotoxicity evaluation of isatin-pyrrole derivatives against HepG2 cell line |
title_short |
Synthesis and in vitro cytotoxicity evaluation of isatin-pyrrole derivatives against HepG2 cell line |
title_full |
Synthesis and in vitro cytotoxicity evaluation of isatin-pyrrole derivatives against HepG2 cell line |
title_fullStr |
Synthesis and in vitro cytotoxicity evaluation of isatin-pyrrole derivatives against HepG2 cell line |
title_full_unstemmed |
Synthesis and in vitro cytotoxicity evaluation of isatin-pyrrole derivatives against HepG2 cell line |
title_sort |
synthesis and in vitro cytotoxicity evaluation of isatin-pyrrole derivatives against hepg2 cell line |
publisher |
De Gruyter |
publishDate |
2021 |
url |
https://doaj.org/article/c1178cb56fdc4d81a52514ff1686c7d5 |
work_keys_str_mv |
AT santosomardi synthesisandinvitrocytotoxicityevaluationofisatinpyrrolederivativesagainsthepg2cellline AT fadlanarif synthesisandinvitrocytotoxicityevaluationofisatinpyrrolederivativesagainsthepg2cellline AT fahmimuhammadrizaghulam synthesisandinvitrocytotoxicityevaluationofisatinpyrrolederivativesagainsthepg2cellline AT rahmayantiardhana synthesisandinvitrocytotoxicityevaluationofisatinpyrrolederivativesagainsthepg2cellline |
_version_ |
1718371806118674432 |