De novo design of chiral organotin cancer drug candidates: Validation of enantiopreferential binding to molecular target DNA and 5′-GMP by UV–visible, fluorescence, 1H and 31P NMR-Reference-Cited by-同舟云学术

De novo design of chiral organotin cancer drug candidates: Validation of enantiopreferential binding to molecular target DNA and 5′-GMP by UV–visible, fluorescence, 1H and 31P NMR

Published:2011-12 Issue:3 Volume:105 Page:167-174
ISSN:1011-1344
Container-title:Journal of Photochemistry and Photobiology B: Biology
language:en
Short-container-title:Journal of Photochemistry and Photobiology B: Biology

Author:

Arjmand Farukh,Sharma Girish Chandra,Sayeed Fatima,Muddassir Mohd.,Tabassum Sartaj

Publisher

Elsevier BV

Subject

Radiology, Nuclear Medicine and imaging,Biophysics,Radiological and Ultrasound Technology,Radiation

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5. Synthesis, characterization and DNA binding studies of penta- and hexa-coordinated diorganotin (IV) 4-(4-nitrophenyl)piperazine-1-carbodithioates;Rehman;J. Organomet. Chem.,2009

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