S
Satish Kumar Awasthi
Researcher at University of Delhi
Publications - 81
Citations - 1919
Satish Kumar Awasthi is an academic researcher from University of Delhi. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 21, co-authored 75 publications receiving 1546 citations. Previous affiliations of Satish Kumar Awasthi include University of Copenhagen & Banaras Hindu University.
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Inhibition of Staphylococcus aureus gene expression and growth using antisense peptide nucleic acids
TL;DR: The present results show that the antisense peptide-PNAs approach can be used to study gene function and requirement in this important pathogen, and further development is needed to raise the antibacterial potential of PNAs.
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Synthesis of newer 1,2,3-triazole linked chalcone and flavone hybrid compounds and evaluation of their antimicrobial and cytotoxic activities.
Rama Kant,Dharmendra Kumar,Drishti Agarwal,Rinkoo D. Gupta,Ragini Tilak,Satish Kumar Awasthi,Alka Agarwal +6 more
TL;DR: The present study was carried out in an attempt to synthesize a new class of antimicrobial and antiplasmodial agents by copper catalyzed click chemistry to afford 25 compounds 10-14(a-e) of 1,4-disubstituted-1,2,3-triazole derivatives of chalcones and flavones.
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Synthesis of novel substituted 1,3-diaryl propenone derivatives and their antimalarial activity in vitro.
Nidhi Mishra,Preeti Arora,Brajesh Kumar,Lokesh C. Mishra,Amit Bhattacharya,Satish Kumar Awasthi,Virendra K. Bhasin +6 more
TL;DR: The synthesis of novel 1,3-diaryl propenone derivatives and their antimalarial activity in vitro against asexual blood stages of human malaria parasite, Plasmodium falciparum, are described and the first report on antiplasmodial activity of chalcones with azoles on acetophenone ring is reported.
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Beta-Hairpin nucleation by Pro-Gly beta-turns. Comparison of D-Pro-Gly and L-Pro-Gly sequences in an apolar octapeptide
TL;DR: The solution conformation of the synthetic octapeptide Boc-Leu-Val-Val, D-Pro-Gly Type II′ β-turns was investigated in organic solvents by NMR spectroscopy as discussed by the authors.
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Design, synthesis and antimicrobial activity of novel benzothiazole analogs.
TL;DR: In an attempt to design and synthesize a new class of antimicrobials, dialkyne substituted 2-aminobenzothiazole was reacted with various substituted aryl azides to generate a small library of 20 compounds by click chemistry, but all compounds were found ineffective against S. boydii (clinical isolate).