Recommanded Product: 123-11-5. Authors De, S; Kumar, RS; Gauthaman, A; Kumar, SKA; Paira, P; Moorthy, A; Banerjee, S in ELSEVIER SCIENCE SA published article about in [De, Sourav; Kumar, R. Selva; Kumar, S. K. Ashok; Paira, Priyankar] Vellore Inst Technol, Sch Adv Sci, Dept Chem, Vellore 632014, Tamil Nadu, India; [Gauthaman, Ashna; Moorthy, Anbalagan] Vellore Inst Technol, Sch Biosci & Technol, Dept Biotechnol, Vellore 632014, Tamil Nadu, India; [Banerjee, Subhasis] Gupta Coll Technol Sci, Dept Pharmaceut Chem, Asansol 713301, W Bengal, India in 2021, Cited 78. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5
Ruthenium complexes are currently significant attention in medicinal chemistry as they offer various properties which make them an appropriate choice for drug development. Herein, a series of ruthenium(II)-p-cymene-2aryl-imidazo-1,10-phenanthroline derivatives have been prepared and characterised by elemental analysis, infrared, LC-mass and NMR techniques. The structural and chemical properties shows that Ru(II) complexes have got rigidity, planarity, aromaticity, hydrogen donating and accepting capability which aids both solubility and interaction with biomolecules. The binding strength of these complexes with DNA and BSA were found to be 10(4)-10(6) M-1. The competitive displacement of ethidium bromide (EtBr) from DNA in the presence of complex reveals an intercalation or groove binding further this was supported by viscosity and in-silico studies. The cytotoxicity study of these Ru(II) complexes were conducted with two cancer cell lines (MDA-MB-231 and HeLa) and one human embryonic kidney cells (HEK-293). The study revealed that [(eta(6)-p-cymene)RuCl (kappa(2)-N,N-2-(4-fluorophenyl)-1H-imidazo[4,5-f][1,10]Phenanthroline]center dot PF6 (4e), [(eta(6)-p-cymene)RuCl(kappa(2)-N,N-2-(4-bromophenyl)-1H-imidazo[4,5-f][1,10]Phenanthroline]center dot PF6 (4f) and [(eta(6)-p-cymene)RuCl(kappa(2)-N,N-2-(4-nitrophenyl)1H-imidazo[4,5-f][1,10]Phenanthro line]center dot PF6 (4g) were found exhibit least inhibitory concentration (IC50) and high selectivity with respect to HeLa and MDA-MB-231. The activity of the Ru(II) complexes were position and substituents dependent.
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Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles