Synthesis, structural characterization and biological activity of 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives: <i>In vitro</i> and <i>in vivo</i> antineoplastic activity

In the present work few novel 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives and the basic compound 2-(4-methylphenylsulfonamido)pentanedioic acid have been synthesized, characterized and screened for their possible antineoplastic activity both in vitro and in vivo. The in vitro...

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Main Authors: Satyajit Dutta, G. Raghava Ravali, Supratim Ray, K. Nagarajan
Format: Article
Language:English
Published: Bangladesh Pharmacological Society 2015-01-01
Series:Bangladesh Journal of Pharmacology
Subjects:
Online Access:https://www.banglajol.info/index.php/BJP/article/view/20748
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author Satyajit Dutta
G. Raghava Ravali
Supratim Ray
K. Nagarajan
author_facet Satyajit Dutta
G. Raghava Ravali
Supratim Ray
K. Nagarajan
author_sort Satyajit Dutta
collection DOAJ
description In the present work few novel 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives and the basic compound 2-(4-methylphenylsulfonamido)pentanedioic acid have been synthesized, characterized and screened for their possible antineoplastic activity both in vitro and in vivo. The in vitro activity was performed against five human cell lines like human breast cancer (MCF-7), leukemia (K-562), ovarian cancer (OVACAR-3), human colon adenocarcinoma (HT-29) and Human kidney carcinoma (A-498). The in vivo activity was performed in female swiss albino mice against Ehrlich ascites carcinoma (EAC). Among the synthesized compounds, ureide, p-bromoanilide, p-nitoanilide, o-bromoanilide and p-methylanilide derivatives of 2-(4-methyl benzene sulphonyl)-pentanedioic acid amides showed encouraging activity in both the in vitro and in vivo compared to other compounds. It was noticed that final derivative compounds show a better activity than the parent compound and it may be due to the substituents present in those compounds.
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spelling doaj.art-2edf13768d454fe08f8d0afcb8e2f1472022-12-22T02:44:58ZengBangladesh Pharmacological SocietyBangladesh Journal of Pharmacology1991-00882015-01-01101Synthesis, structural characterization and biological activity of 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives: <i>In vitro</i> and <i>in vivo</i> antineoplastic activitySatyajit Dutta0G. Raghava Ravali1Supratim Ray2K. Nagarajan3Department of Pharmaceutical Chemistry, IIMT College of Medical Sciences, Meerut 250001, Uttar PradeshDepartment of Pharmaceutical Chemistry, Dr. B. C. Roy College of Pharmacy & Allied Health Sciences, Durgapur 713206, West BengalDepartment of Pharmaceutical Sciences, Assam University, Silchar 788011, AssamDepartment of Pharmaceutical Chemistry, KIET School of Pharmacy, Muradnagar, Ghaziabad 201206, Uttar PradeshIn the present work few novel 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives and the basic compound 2-(4-methylphenylsulfonamido)pentanedioic acid have been synthesized, characterized and screened for their possible antineoplastic activity both in vitro and in vivo. The in vitro activity was performed against five human cell lines like human breast cancer (MCF-7), leukemia (K-562), ovarian cancer (OVACAR-3), human colon adenocarcinoma (HT-29) and Human kidney carcinoma (A-498). The in vivo activity was performed in female swiss albino mice against Ehrlich ascites carcinoma (EAC). Among the synthesized compounds, ureide, p-bromoanilide, p-nitoanilide, o-bromoanilide and p-methylanilide derivatives of 2-(4-methyl benzene sulphonyl)-pentanedioic acid amides showed encouraging activity in both the in vitro and in vivo compared to other compounds. It was noticed that final derivative compounds show a better activity than the parent compound and it may be due to the substituents present in those compounds.https://www.banglajol.info/index.php/BJP/article/view/20748Glutamic acid (2-amino pentanedioic acid)AnticancerMTT assayEhrlich ascites carcinoma.
spellingShingle Satyajit Dutta
G. Raghava Ravali
Supratim Ray
K. Nagarajan
Synthesis, structural characterization and biological activity of 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives: <i>In vitro</i> and <i>in vivo</i> antineoplastic activity
Bangladesh Journal of Pharmacology
Glutamic acid (2-amino pentanedioic acid)
Anticancer
MTT assay
Ehrlich ascites carcinoma.
title Synthesis, structural characterization and biological activity of 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives: <i>In vitro</i> and <i>in vivo</i> antineoplastic activity
title_full Synthesis, structural characterization and biological activity of 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives: <i>In vitro</i> and <i>in vivo</i> antineoplastic activity
title_fullStr Synthesis, structural characterization and biological activity of 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives: <i>In vitro</i> and <i>in vivo</i> antineoplastic activity
title_full_unstemmed Synthesis, structural characterization and biological activity of 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives: <i>In vitro</i> and <i>in vivo</i> antineoplastic activity
title_short Synthesis, structural characterization and biological activity of 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives: <i>In vitro</i> and <i>in vivo</i> antineoplastic activity
title_sort synthesis structural characterization and biological activity of 2 4 methylbenzenesulphonamido pentanedioic acid amide derivatives i in vitro i and i in vivo i antineoplastic activity
topic Glutamic acid (2-amino pentanedioic acid)
Anticancer
MTT assay
Ehrlich ascites carcinoma.
url https://www.banglajol.info/index.php/BJP/article/view/20748
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