Chronophysiological features of the normal mineral composition of human saliva

Fused pyrimidine derivatives R 0515Synthesis Leading to Novel 2,4,6-Trisubstituted Quinazoline Derivatives, Their Antibacterial and Cytotoxic Activity Against THP-1, HL-60 and A375 Cell Lines.-Twelve 2,4,6-Trisubstituted quinazoline derivatives of type (V) are prepared and screened for their antibacterial and cytotoxic effects against the title cell lines. Derivative (Vd) exhibits the highest activity against THP-1 and HL-60 cell lines, whereas (Va) and (Vb) show moderate activity. -(CHANDRIKA, P. M.; YAKAIAH, T.; NARSAIAH*, B.; SRIDHAR, V.; VENUGOPAL, G.; RAO, J. V.; KUMAR, K. P.; MURTHY, U. S. N.; RAO, A. R. R.; Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 48 (2009) 6, 840-847; Fluoroorg. Div., Indian Inst. Chem. Technol., Hyderabad 500 007, India; Eng.) -M. Bohle 43-171

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Anti-inflammatory potential of thienopyridines as possible alternative to NSAIDs

Kuncha

Boyapati

Naidu

et al. 2012

European Journal of Pharmacology

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Click chemistry: Studies on the synthesis of novel fluorous tagged triazol-4-yl substituted quinazoline derivatives and their biological evaluation – Theoretical and experimental validation

Chandrika

Yakaiah

Gayatri

et al. 2010

European Journal of Medicinal Chemistry

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Synthesis and structure–activity relationships of novel pyrimido[1,2-b]indazoles as potential anticancer agents against A-549 cell lines

Yakaiah

Lingaiah

Narsaiah

et al. 2007

Bioorganic & Medicinal Chemistry Letters

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ChemInform Abstract: Synthesis Leading to Novel 2,4,6‐Trisubstituted Quinazoline Derivatives, Their Antibacterial and Cytotoxic Activity Against THP‐1, HL‐60 and A375 Cell Lines.

Anti-inflammatory potential of thienopyridines as possible alternative to NSAIDs

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Synthesis and structure–activity relationships of novel pyrimido[1,2-b]indazoles as potential anticancer agents against A-549 cell lines

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