Solvent-dependent crystallization and anti-cancer activities based on Ni(II) and Co(II) complexes of 1-picolinoyl-4-phenyl-3-thiosemicarbazide: Synthesis, crystal structure, and photoluminescence study
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Chandra, Suryansh
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Banaras Hindu Univ, Dept Chem, Varanasi 221005, IndiaBanaras Hindu Univ, Dept Chem, Varanasi 221005, India
Chandra, Suryansh
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Jaiswal, Shubham
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Banaras Hindu Univ, Dept Chem, Varanasi 221005, IndiaBanaras Hindu Univ, Dept Chem, Varanasi 221005, India
Jaiswal, Shubham
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Shukla, Alok
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Banaras Hindu Univ, Dept Zool, Varanasi 221005, IndiaBanaras Hindu Univ, Dept Chem, Varanasi 221005, India
Shukla, Alok
[2
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Singh, Ankit Kumar
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Garai, Somenath
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Banaras Hindu Univ, Dept Chem, Varanasi 221005, IndiaBanaras Hindu Univ, Dept Chem, Varanasi 221005, India
Garai, Somenath
[1
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Bharti, A.
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Univ Delhi, Kirori Mal Coll, Dept Chem, Delhi 110007, IndiaBanaras Hindu Univ, Dept Chem, Varanasi 221005, India
Bharti, A.
[3
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Acharya, A.
[2
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Bharty, M. K.
[1
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[1] Banaras Hindu Univ, Dept Chem, Varanasi 221005, India
[2] Banaras Hindu Univ, Dept Zool, Varanasi 221005, India
[3] Univ Delhi, Kirori Mal Coll, Dept Chem, Delhi 110007, India
In search of alternative of platinum-based drugs for the treatment of cancer, lead to the development of other potential metallodrug of transition metal complexes. The efficacious and novel experimental content of this paper reports the synthesis of [Ni(Hppts)(2)].CHCl3 (1a), [Ni(Hppts)(2)].(CH3)(2)SO (1b) and [Co(Hppts)(2)] (2) complexes of 1-picolinoyl-4-phenyl-3-thiosemicarbazide (H2ppts). The synthesized complexes have been characterized by UV-vis., Infrared, and NMR spectrometry. Furthermore, complexes 1a and 1b were characterized by single-crystal X-ray diffraction data. Emission spectra show that, complex 1a exhibits higher fluorescence intensity as compared to that of ligand H2ppts and complex 2. The order of fluorescence intensity was found as complex 1a > complex 2 > H2ppts. Moreover, Complexes 1a and 1b are stabilized via various types of intermolecular interactions. The cytotoxicity of complexes 1a, 2, and ligand was evaluated against Dalton's Lymphoma cells using standard MTT Assay. The anticancer activity results showed that complex 1a significantly reduced cell viability in a dose-dependent manner, whereas H2ppts and complex 2 did not show significant reduction in cell viability of DL cells when compared with the control. The complex 1a IC50 value was determined to be around 40 mu g/mL. The anti-tumor activity concludes that the complex 1a has high anti-neoplastic activity on DL cells at low doses.
机构:
Inorganic Chemistry Section, Department of Chemistry, Jadavpur University, Kolkata,700032, IndiaInorganic Chemistry Section, Department of Chemistry, Jadavpur University, Kolkata,700032, India
Naskar, Rahul
Ghosh, Paramita
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Department of Signal Transduction and Biogenic Amines (STBA), Chittaranjan National Cancer Institute, Kolkata,700026, IndiaInorganic Chemistry Section, Department of Chemistry, Jadavpur University, Kolkata,700032, India
Ghosh, Paramita
Manna, Chandan Kumar
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Inorganic Chemistry Section, Department of Chemistry, Jadavpur University, Kolkata,700032, IndiaInorganic Chemistry Section, Department of Chemistry, Jadavpur University, Kolkata,700032, India
Manna, Chandan Kumar
Murmu, Nabendu
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Department of Signal Transduction and Biogenic Amines (STBA), Chittaranjan National Cancer Institute, Kolkata,700026, IndiaInorganic Chemistry Section, Department of Chemistry, Jadavpur University, Kolkata,700032, India
Murmu, Nabendu
Mondal, Tapan Kumar
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Inorganic Chemistry Section, Department of Chemistry, Jadavpur University, Kolkata,700032, IndiaInorganic Chemistry Section, Department of Chemistry, Jadavpur University, Kolkata,700032, India
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Southern Fed Univ, Res Inst Phys & Organ Chem, Pr Stachki 194-2, Rostov Na Donu 344090, RussiaSouthern Fed Univ, Res Inst Phys & Organ Chem, Pr Stachki 194-2, Rostov Na Donu 344090, Russia
Burlov, A. S.
Koshchienko, Yu. V.
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Southern Fed Univ, Res Inst Phys & Organ Chem, Pr Stachki 194-2, Rostov Na Donu 344090, RussiaSouthern Fed Univ, Res Inst Phys & Organ Chem, Pr Stachki 194-2, Rostov Na Donu 344090, Russia
Koshchienko, Yu. V.
Vlasenko, V. G.
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Southern Fed Univ, Inst Phys Res, Pr Stachki 194, Rostov Na Donu 344090, RussiaSouthern Fed Univ, Res Inst Phys & Organ Chem, Pr Stachki 194-2, Rostov Na Donu 344090, Russia
Vlasenko, V. G.
Chesnokov, V. V.
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Southern Fed Univ, Res Inst Phys & Organ Chem, Pr Stachki 194-2, Rostov Na Donu 344090, RussiaSouthern Fed Univ, Res Inst Phys & Organ Chem, Pr Stachki 194-2, Rostov Na Donu 344090, Russia
Chesnokov, V. V.
Revinskii, Yu. V.
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Russian Acad Sci, Southern Sci Ctr, Ul Chekhova 41, Rostov Na Donu 344006, RussiaSouthern Fed Univ, Res Inst Phys & Organ Chem, Pr Stachki 194-2, Rostov Na Donu 344090, Russia
Revinskii, Yu. V.
Zubavichus, Ya. V.
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Natl Res Ctr, Kurchatov Inst, Pl Akad Kurchatova 1, Moscow 123182, RussiaSouthern Fed Univ, Res Inst Phys & Organ Chem, Pr Stachki 194-2, Rostov Na Donu 344090, Russia
Zubavichus, Ya. V.
Trigub, A. L.
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Natl Res Ctr, Kurchatov Inst, Pl Akad Kurchatova 1, Moscow 123182, RussiaSouthern Fed Univ, Res Inst Phys & Organ Chem, Pr Stachki 194-2, Rostov Na Donu 344090, Russia
Trigub, A. L.
Garnovskii, D. A.
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Russian Acad Sci, Southern Sci Ctr, Ul Chekhova 41, Rostov Na Donu 344006, RussiaSouthern Fed Univ, Res Inst Phys & Organ Chem, Pr Stachki 194-2, Rostov Na Donu 344090, Russia
Garnovskii, D. A.
Uraev, A. I.
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Southern Fed Univ, Res Inst Phys & Organ Chem, Pr Stachki 194-2, Rostov Na Donu 344090, RussiaSouthern Fed Univ, Res Inst Phys & Organ Chem, Pr Stachki 194-2, Rostov Na Donu 344090, Russia