Literature DB >> 26347024

Synthesis, characterization and in vitro evaluation of novel enantiomerically-pure sulphonamide antimalarials.

Sebastian Anusha1, Ameya Sinha2, C P Babu Rajeev1, Trang T T Chu2, Jessin Mathai3, Huang Ximei4, Julian E Fuchs5, NanjundaSwamy Shivananju6, Andreas Bender7, Peter Rainer Preiser4, Kanchugarakoppal S Rangappa6, Rajesh Chandramohanadas2.   

Abstract

Malaria parasites are currently gaining drug-resistance rapidly, across countries and continents. Hence, the discovery and development of novel chemical scaffolds, with superior antimalarial activity remain an important priority, for the developing world. Our report describes the development, characterization and evaluation of novel bepotastine-based sulphonamide antimalarials inhibiting asexual stage development of Plasmodium falciparum parasites in vitro. The screening results showed potent inhibitory activity of a number of novel sulphonamides against P. falciparum at low micromolar concentrations, in particular in late-stage parasite development. Based on computational studies we hypothesize N-myristoyltransferase as the target of the compounds developed here. Our results demonstrate the value of novel bepotastine-based sulphonamide compounds for targeting the asexual developmental stages of P. falciparum.

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Year:  2015        PMID: 26347024     DOI: 10.1039/c5ob01479d

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  Targeted Phenotypic Screening in Plasmodium falciparum and Toxoplasma gondii Reveals Novel Modes of Action of Medicines for Malaria Venture Malaria Box Molecules.

Authors:  Gowtham Subramanian; Meenakshi A Belekar; Anurag Shukla; Jie Xin Tong; Ameya Sinha; Trang T T Chu; Akshay S Kulkarni; Peter R Preiser; D Srinivasa Reddy; Kevin S W Tan; Dhanasekaran Shanmugam; Rajesh Chandramohanadas
Journal:  mSphere       Date:  2018-01-17       Impact factor: 4.389

2.  Synthesis, carbonic anhydrase I and II inhibition studies of the 1,3,5-trisubstituted-pyrazolines.

Authors:  Halise Inci Gul; Ebru Mete; Parham Taslimi; Ilhami Gulcin; Claudiu T Supuran
Journal:  J Enzyme Inhib Med Chem       Date:  2016-10-24       Impact factor: 5.051

  2 in total

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