N. Dastagiri Reddy
Pondicherry University
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RSC Advances | 2014
A. Haleel; P. Arthi; N. Dastagiri Reddy; V. Veena; N. Sakthivel; Y. Arun; P. T. Perumal; A. Kalilur Rahiman
Six mononuclear copper(II), nickel(II) and zinc(II) complexes, [ML1Cl2] (1–3) and [M(L2)2Cl2] (4–6), of two biologically active tetrazolo[1,5-a]pyrimidine core ligands, ethyl 5-methyl-7-pyridine-2-yl-4,7-dihydrotetrazolo[1,5-a]pyrimidine-6-carboxylate (L1) and ethyl-5-methyl-7-pyridine-4-yl-4,7-dihydrotetrazolo[1,5-a]pyrimidine-6-carboxylate (L2), have been synthesized and characterized. The molecular structure of the ligands (L1&2) and complex 6 were determined by single crystal X-ray diffraction. The X-ray crystal structure of 6 confirms that it has a distorted tetrahedral structure with a ZnN2Cl2 coordination environment. All of the complexes exhibit an unusually strong luminescence at room temperature. Electroparamagnetic resonance spectra of copper(II) complexes (2 and 5) show four lines, characteristic of square planar geometry, with nuclear hyperfine spin 3/2. DNA binding studies of complexes with calf-thymus DNA suggest that complexes 2 and 5 bind in the grooves of the DNA. These results were further supported by molecular docking studies. In vitro cytotoxic activities of the ligands (L1&2) and complexes (1–6) against human cancer cell lines such as lung (A549), cervical (HeLa), colon (HCT-15) and a non-cancer human embryonic kidney cell line revealed that the complexes selectively inhibit the growth of cancer cells and are inactive against non-cancer cell lines, whereas the ligands were found to be inactive with both cancer and non-cancer cell lines. The IC50 values of the complexes revealed that the copper(II) complexes (2 and 5) exhibit high cytotoxic activity against colon (HCT-15) cells when compared to the standard drug cisplatin. Furthermore, the live cell and fluorescent imaging of cancer cells show that complexes 2 and 5 induce cell death through apoptosis.
Archive | 2017
B. Raghavendra; K. Bakthavachalam; Buthanapalli Ramakrishna; N. Dastagiri Reddy
Related Article: B. Raghavendra, K. Bakthavachalam, Buthanapalli Ramakrishna, N. Dastagiri Reddy|2017|Organometallics|||doi:10.1021/acs.organomet.7b00617
Archive | 2017
B. Raghavendra; K. Bakthavachalam; Buthanapalli Ramakrishna; N. Dastagiri Reddy
Related Article: B. Raghavendra, K. Bakthavachalam, Buthanapalli Ramakrishna, N. Dastagiri Reddy|2017|Organometallics|36|4005|doi:10.1021/acs.organomet.7b00617
Inorganic Chemistry | 2003
Marcus Schiefer; N. Dastagiri Reddy; Hans‐Jürgen Ahn; Andreas Stasch; Herbert W. Roesky; A. Christine Schlicker; Hans-Georg Schmidt; Mathias Noltemeyer; Denis Vidovic
Organometallics | 2003
Marcus Schiefer; N. Dastagiri Reddy; Herbert W. Roesky; Denis Vidovic
Organometallics | 2013
K. Bakthavachalam; N. Dastagiri Reddy
Inorganic Chemistry | 2002
N. Dastagiri Reddy; Herbert W. Roesky; Mathias Noltemeyer; Hans-Georg Schmidt
Dalton Transactions | 2010
N. Dastagiri Reddy; Anukul Jana; Herbert W. Roesky; Prinson P. Samuel; Carola Schulzke
Organometallics | 2003
S. Shravan Kumar; N. Dastagiri Reddy; Herbert W. Roesky; Denis Vidovic; Jörg Magull; Rainer F. Winter
Organometallics | 2010
K. Maheswari; N.M. Rajendran; Jens Meyer; N. Dastagiri Reddy