Inorganic Chemistry, volume 56, issue 20, pages 12232-12247
Anticancer Activity of Iridium(III) Complexes Based on a Pyrazole-Appended Quinoline-Based BODIPY.
Publication type: Journal Article
Publication date: 2017-09-28
Journal:
Inorganic Chemistry
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 4.6
ISSN: 00201669, 1520510X
Inorganic Chemistry
Physical and Theoretical Chemistry
Abstract
A pyrazole-appended quinoline-based 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (L1, BODIPY) has been synthesized and used as a ligand for the preparation of iridium(III) complexes [Ir(phpy)2(L1)]PF6 (1; phpy = 2-phenylpyridine) and [(η5-C5Me5)Ir(L1)Cl]PF6 (2). The ligand L1 and complexes 1 and 2 have been meticulously characterized by elemental analyses and spectral studies (IR, electrospray ionization mass spectrometry, 1H and 13C NMR, UV/vis, fluorescence) and their structures explicitly authenticated by single-crystal X-ray analyses. UV/vis, fluorescence, and circular dichroism studies showed that complexes strongly bind with calf-thymus DNA and bovine serum albumin. Molecular docking studies clearly illustrated binding through DNA minor grooves via van der Waals forces and their electrostatic interaction and occurrence in the hydrophobic cavity of protein (subdomain IIA). Cytotoxicity, morphological changes, and apoptosis have been explored by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and Hoechst 33342 staining. IC50 values for complexes (1, 30 μM; 2, 50 μM) at 24 h toward the human cervical cancer cell line (HeLa) are as good as that of cisplatin (21.6 μM) under analogous conditions, and their ability to kill cancer cells lies in the order 1 > 2. Because of the inherent emissive nature of the BODIPY moiety, these are apt for intracellular visualization at low concentration and may find potential applications in cellular imaging and behave as a theranostic agent.
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- We do not take into account publications that without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
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Paitandi R. P. et al. Anticancer Activity of Iridium(III) Complexes Based on a Pyrazole-Appended Quinoline-Based BODIPY. // Inorganic Chemistry. 2017. Vol. 56. No. 20. pp. 12232-12247.
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Paitandi R. P., Mukhopadhyay S., Singh R., Sharma V. S., Mobin S. M., Pandey D. S. Anticancer Activity of Iridium(III) Complexes Based on a Pyrazole-Appended Quinoline-Based BODIPY. // Inorganic Chemistry. 2017. Vol. 56. No. 20. pp. 12232-12247.
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TY - JOUR
DO - 10.1021/acs.inorgchem.7b01693
UR - https://doi.org/10.1021%2Facs.inorgchem.7b01693
TI - Anticancer Activity of Iridium(III) Complexes Based on a Pyrazole-Appended Quinoline-Based BODIPY.
T2 - Inorganic Chemistry
AU - Paitandi, Rajendra Prasad
AU - Mukhopadhyay, Sujay
AU - Mobin, Shaikh M.
AU - Pandey, Daya Shankar
AU - Singh, Roop
AU - Sharma, Vinay S.
PY - 2017
DA - 2017/09/28 00:00:00
PB - American Chemical Society (ACS)
SP - 12232-12247
IS - 20
VL - 56
SN - 0020-1669
SN - 1520-510X
ER -
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@article{2017_Paitandi,
author = {Rajendra Prasad Paitandi and Sujay Mukhopadhyay and Shaikh M. Mobin and Daya Shankar Pandey and Roop Singh and Vinay S. Sharma},
title = {Anticancer Activity of Iridium(III) Complexes Based on a Pyrazole-Appended Quinoline-Based BODIPY.},
journal = {Inorganic Chemistry},
year = {2017},
volume = {56},
publisher = {American Chemical Society (ACS)},
month = {sep},
url = {https://doi.org/10.1021%2Facs.inorgchem.7b01693},
number = {20},
pages = {12232--12247},
doi = {10.1021/acs.inorgchem.7b01693}
}
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Paitandi, Rajendra Prasad, et al. “Anticancer Activity of Iridium(III) Complexes Based on a Pyrazole-Appended Quinoline-Based BODIPY..” Inorganic Chemistry, vol. 56, no. 20, Sep. 2017, pp. 12232-12247. https://doi.org/10.1021%2Facs.inorgchem.7b01693.
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