TY - JOUR
T1 - Multistage inhibitors of the malaria parasite
T2 - Emerging hope for chemoprotection and malaria eradication
AU - Poonam,
AU - Gupta, Yash
AU - Gupta, Nikesh
AU - Singh, Snigdha
AU - Wu, Lidong
AU - Chhikara, Bhupender Singh
AU - Rawat, Manmeet
AU - Rathi, Brijesh
N1 - Funding Information:
Science and Engineering Research Board, Grant/Award Number: ECR/2015/000448; University Grants Commission, Grant/Award Number: F.30-375/2017 (BSR)
Funding Information:
We are thankful to the Science and Engineering Research Board, New Delhi and the Government of India for financial aid (ECR/2015/000448). Poonam is grateful to University Grants Commission for the UGC-BSR Research Start-Up Grant No. F.30-375/2017 (BSR). BR, an UGC-Raman postdoctoral fellow at MIT, is highly grateful to his advisor, Prof. Alexander M Klibanov, Novartis-Chair Professor, Department of Chemistry, MIT, for his suggestions and encouragement. NG acknowledges UGC for DSK Post-Doctoral fellowship.
Funding Information:
Nikesh Gupta earned his Bachelor's and Master's degree in Chemistry from Hindu Col-lege, University of Delhi. He completed his M.Phil. and Ph.D. from Department of Chem-istry, University of Delhi, in the field of material sciences and nanomedicine, respectively. During his Ph.D., he has worked on two different research projects sponsored by Depart-ment of Science and Technology (DST) and University Grants Commission (UGC), India and received the prestigious senior research fellowship (SRF) sponsored by Council of Sci-entific and Industrial Research (CSIR), India. He has been awarded Dr. D.S. Kothari PostDoctoral Research Fellowship by UGC, India. Currently he is pursuing his postdoctoral research at Special Centre for Nanosciences, Jawaharlal Nehru University, India. He has presented his research papers in various national and international conferences for which he has been awarded with best poster awards and published quality papers in reputed international journals of high impact factor. His area of research majorly focuses on synthesis and characterizations of inorganic/magnetic/polymeric nanoparticles with their applications in cancer therapy, gene delivery, and as antibacterial and MRI contrast agents.
Publisher Copyright:
© 2018 Wiley Periodicals, Inc.
PY - 2018/9
Y1 - 2018/9
N2 - Over time, several exciting advances have been made in the treatment and prevention of malaria; however, this devastating disease continues to be a major global health problem and affects millions of people every year. Notably, the paucity of new efficient drug molecules and the inevitable drug resistance of the malaria parasite, Plasmodium falciparum, against frontline therapeutics are the foremost struggles facing malaria eradication initiatives. According to the malaria eradication agenda, the discovery of new chemical entities that can destroy the parasite at the liver stage, the asexual blood stage, the gametocyte stage, and the insect ookinete stage of the parasite life cycle (i.e., compounds exhibiting multistage activity) are in high demand, preferably with novel and multiple modes of action. Phenotypic screening of chemical libraries against the malaria parasite is certainly a crucial step toward overcoming these crises. In the last few years, various research groups, including industrial research laboratories, have performed large-scale phenotypic screenings that have identified a wealth of chemical entities active against multiple life stages of the malaria parasite. Vital scientific and technological developments have led to the discovery of multistage inhibitors of the malaria parasite; these compounds, considered highly valuable starting points for subsequent drug discovery and eradication of malaria, are reviewed.
AB - Over time, several exciting advances have been made in the treatment and prevention of malaria; however, this devastating disease continues to be a major global health problem and affects millions of people every year. Notably, the paucity of new efficient drug molecules and the inevitable drug resistance of the malaria parasite, Plasmodium falciparum, against frontline therapeutics are the foremost struggles facing malaria eradication initiatives. According to the malaria eradication agenda, the discovery of new chemical entities that can destroy the parasite at the liver stage, the asexual blood stage, the gametocyte stage, and the insect ookinete stage of the parasite life cycle (i.e., compounds exhibiting multistage activity) are in high demand, preferably with novel and multiple modes of action. Phenotypic screening of chemical libraries against the malaria parasite is certainly a crucial step toward overcoming these crises. In the last few years, various research groups, including industrial research laboratories, have performed large-scale phenotypic screenings that have identified a wealth of chemical entities active against multiple life stages of the malaria parasite. Vital scientific and technological developments have led to the discovery of multistage inhibitors of the malaria parasite; these compounds, considered highly valuable starting points for subsequent drug discovery and eradication of malaria, are reviewed.
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U2 - 10.1002/med.21486
DO - 10.1002/med.21486
M3 - Review article
C2 - 29372568
AN - SCOPUS:85049716944
SN - 0198-6325
VL - 38
SP - 1511
EP - 1535
JO - Medicinal Research Reviews
JF - Medicinal Research Reviews
IS - 5
ER -