Synthesis, in vitro cytotoxic, anti-Mycobacterium tuberculosis and molecular docking studies of 4-pyridylamino- and 4-(ethynylpyridine)quinazolines

Author:

Dilebo Kabelo B.ORCID,Gumede Njabulo J.ORCID,Nxumalo Winston,Matsebatlela Thabe M.,Mangokoana DikgaleORCID,Moraone Ngaoko R.,Omondi BernardORCID,Mampa Richard M.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference62 articles.

1. Tuberculosis: a disease without boundaries;Fogel;Tuberculosis,2015

2. Global tuberculosis report 2018; Licence: CC BY-NC-SA 3.0 IGO; WHO/CDS/TB/2018.20,2018

3. Quinazolinone and quinazoline derivatives: recent structures with potent antimicrobial and cytotoxic activities;Jafara;Res. Pharm. Sci.,2016

4. Synthesis, biological evaluation and molecular docking of novel indole-aminoquinazoline hybrids for anticancer properties;Mphahlele;Int. J. Mol. Sci.,2018

5. Novel 2, 3-disubstituted quinazoline-4(3H)-one molecules derived from amino acid linked sulphonamide as a potent malarial antifolates for DHFR inhibition;Patel;Eur. J. Med. Chem.,2017

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