Design, synthesis, and anticancer evaluation of 1,2,4-oxadiazole functionalized quinoline derivatives
- 1. Acharya Nagarjuna University. Department of Chemistry (India)
- 2. Adikavi Nannaya University. Department of Chemistry (India)
Description
A library of 1,2,4-oxadiazole functionalized quinoline derivatives (13a–j) were synthesized and their structures were confirmed by 1H NMR, 13C NMR and Mass Spectral analysis. Further, these compounds were evaluated for their anticancer activity against four human cancer cell lines, namely MCF-7 (breast), A549 (lung), DU-145 (prostate) and MDA MB-231 (breast) using Etoposide as the positive control. Most of these derivatives exhibited more potent activity towards the four cancer cell lines compared to Etoposide. Amongst all the compounds tested, compounds 13b, 13c, 13h, 13i and 13j exhibited promising activity. Further of these compounds 13b, 13i and 13j exhibited excellent activity, when compared with Etoposide.
Additional details
Identifiers
Publishing Information
- Journal Title
- Medicinal Chemistry Research (Print)
- Journal Volume
- 29
- Journal Issue
- 1
- Journal Page Range
- p. 136-144
- ISSN
- 1054-2523
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 55088653
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- BENZIMIDAZOLES; BIOSYNTHESIS; CARBON 13; CHEMICAL SHIFT; EVALUATION; HYDROGEN 1; LUNGS; MAMMARY GLANDS; MASS SPECTRA; NEOPLASMS; PROSTATE; TUMOR CELLS
- Descriptors DEC
- ANIMAL CELLS; AZOLES; BODY; CARBON ISOTOPES; DISEASES; EVEN-ODD NUCLEI; GLANDS; HETEROCYCLIC COMPOUNDS; HYDROGEN ISOTOPES; IMIDAZOLES; ISOTOPES; LIGHT NUCLEI; MALE GENITALS; NUCLEI; ODD-EVEN NUCLEI; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANS; RESPIRATORY SYSTEM; SPECTRA; STABLE ISOTOPES; SYNTHESIS
Optional Information
- Copyright
- Copyright (c) 2019 © Springer Science+Business Media, LLC, part of Springer Nature 2019