Synthesis of 3-(2-(subsituted-(trifluoromethyl)phenylamino)acetyl)-2H-chromen-2-one derivatives as new anticancer agents

Under solvent free conditions and in presence of a base 3-(2-(subsituted-(trifluoromethyl)phenylamino)acetyl)-2H-chromen-2-one derivatives were synthesized by grinding technique. Structural investigations were carried out with IR studies, HRMS, 1HNMR and 13CNMR. The compounds were checked f...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Anees Pangal, Yusufi Mujahid, Bajarang Desai, Javed A. Shaikh, Khursheed Ahmed
Formato: article
Lenguaje:EN
Publicado: Growing Science 2022
Materias:
Acceso en línea:https://doaj.org/article/a7d048a987514ad3be380889d499943f
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:a7d048a987514ad3be380889d499943f
record_format dspace
spelling oai:doaj.org-article:a7d048a987514ad3be380889d499943f2021-11-12T12:52:42ZSynthesis of 3-(2-(subsituted-(trifluoromethyl)phenylamino)acetyl)-2H-chromen-2-one derivatives as new anticancer agents1927-72961927-730X10.5267/j.ccl.2021.8.004https://doaj.org/article/a7d048a987514ad3be380889d499943f2022-01-01T00:00:00Zhttp://www.growingscience.com/ccl/Vol11/ccl_2021_31.pdfhttps://doaj.org/toc/1927-7296https://doaj.org/toc/1927-730X Under solvent free conditions and in presence of a base 3-(2-(subsituted-(trifluoromethyl)phenylamino)acetyl)-2H-chromen-2-one derivatives were synthesized by grinding technique. Structural investigations were carried out with IR studies, HRMS, 1HNMR and 13CNMR. The compounds were checked for their in vitro anticancer activities against three different human cancer cell lines viz human breast cancer cell line (MCF-7), human cervical cancer cell line (HeLa) and human oral squamous cell carcinoma (SCC-40) using SRB method. All the title compounds showed low toxicity towards non-malignant PBMC cells indicating their tumour selectivity. The compounds exhibited good in vitro anti-proliferative potency at lower concentrations against HeLa and MCF-7 cell lines and remain moderately active against SCC-40.Anees PangalYusufi MujahidBajarang DesaiJaved A. ShaikhKhursheed AhmedGrowing SciencearticleChemistryQD1-999ENCurrent Chemistry Letters, Vol 11, Iss 1, Pp 105-112 (2022)
institution DOAJ
collection DOAJ
language EN
topic Chemistry
QD1-999
spellingShingle Chemistry
QD1-999
Anees Pangal
Yusufi Mujahid
Bajarang Desai
Javed A. Shaikh
Khursheed Ahmed
Synthesis of 3-(2-(subsituted-(trifluoromethyl)phenylamino)acetyl)-2H-chromen-2-one derivatives as new anticancer agents
description Under solvent free conditions and in presence of a base 3-(2-(subsituted-(trifluoromethyl)phenylamino)acetyl)-2H-chromen-2-one derivatives were synthesized by grinding technique. Structural investigations were carried out with IR studies, HRMS, 1HNMR and 13CNMR. The compounds were checked for their in vitro anticancer activities against three different human cancer cell lines viz human breast cancer cell line (MCF-7), human cervical cancer cell line (HeLa) and human oral squamous cell carcinoma (SCC-40) using SRB method. All the title compounds showed low toxicity towards non-malignant PBMC cells indicating their tumour selectivity. The compounds exhibited good in vitro anti-proliferative potency at lower concentrations against HeLa and MCF-7 cell lines and remain moderately active against SCC-40.
format article
author Anees Pangal
Yusufi Mujahid
Bajarang Desai
Javed A. Shaikh
Khursheed Ahmed
author_facet Anees Pangal
Yusufi Mujahid
Bajarang Desai
Javed A. Shaikh
Khursheed Ahmed
author_sort Anees Pangal
title Synthesis of 3-(2-(subsituted-(trifluoromethyl)phenylamino)acetyl)-2H-chromen-2-one derivatives as new anticancer agents
title_short Synthesis of 3-(2-(subsituted-(trifluoromethyl)phenylamino)acetyl)-2H-chromen-2-one derivatives as new anticancer agents
title_full Synthesis of 3-(2-(subsituted-(trifluoromethyl)phenylamino)acetyl)-2H-chromen-2-one derivatives as new anticancer agents
title_fullStr Synthesis of 3-(2-(subsituted-(trifluoromethyl)phenylamino)acetyl)-2H-chromen-2-one derivatives as new anticancer agents
title_full_unstemmed Synthesis of 3-(2-(subsituted-(trifluoromethyl)phenylamino)acetyl)-2H-chromen-2-one derivatives as new anticancer agents
title_sort synthesis of 3-(2-(subsituted-(trifluoromethyl)phenylamino)acetyl)-2h-chromen-2-one derivatives as new anticancer agents
publisher Growing Science
publishDate 2022
url https://doaj.org/article/a7d048a987514ad3be380889d499943f
work_keys_str_mv AT aneespangal synthesisof32subsitutedtrifluoromethylphenylaminoacetyl2hchromen2onederivativesasnewanticanceragents
AT yusufimujahid synthesisof32subsitutedtrifluoromethylphenylaminoacetyl2hchromen2onederivativesasnewanticanceragents
AT bajarangdesai synthesisof32subsitutedtrifluoromethylphenylaminoacetyl2hchromen2onederivativesasnewanticanceragents
AT javedashaikh synthesisof32subsitutedtrifluoromethylphenylaminoacetyl2hchromen2onederivativesasnewanticanceragents
AT khursheedahmed synthesisof32subsitutedtrifluoromethylphenylaminoacetyl2hchromen2onederivativesasnewanticanceragents
_version_ 1718430514212241408