Naveen Shivalingegowda

Bio: Naveen Shivalingegowda is an academic researcher from Jain University. The author has contributed to research in topics: Crystal structure & Monoclinic crystal system. The author has an hindex of 8, co-authored 34 publications receiving 196 citations. Previous affiliations of Naveen Shivalingegowda include University of Mysore.

Synthesis of cocrystals/salts of flucytosine: Structure and stability

Abstract: 5-Fluorocytosine or flucytosine (FLC) is a well-known drug for anti-fungal treatment and is one of the essential medicines needed in a health system. The main disadvantage of FLC drugs is their instability due to hydration under storage conditions. In the present work, cocrystal/salt screening experiments resulted in three molecular salts of FLC with dihydroxybenzoic acid derivatives, 2,3-dihydroxybenzoic acid (2,3HBA), 3,5-dihydroxybenzoic acid (3,5HBA), and 2,6-dihydroxybenzoic acid (2,6HBA), and two cocrystals with gallic acid (GAA) and glutaric acid (GLA). Since FLC drugs are highly susceptible to hydration, the present work concentrated on the stability of the synthesized molecular salts/cocrystals under different relative humidity (RH) conditions. All the newly formed crystalline adducts were characterized structurally, and the crystal structures were determined using single-crystal X-ray diffraction techniques (SCXRD). The FLC–2,6HBA salt was found to be a monohydrate, whereas the FLC–3,5HBA salt was crystallized as a hemipentahydrate. FLC–2,3HBA and FLC–GLA were crystallized in 2 : 1 equimolar ratios of FLC and the coformer. The FLC–GAA cocrystal crystallized in a 1 : 1 equimolar ratio. Two point heterosynthons between FLC and the coformer were observed in all the crystalline structures except FLC–GLA, where the structure was formed through a single point heterosynthon. Stability studies under different relative humidity conditions showed the non-hygroscopicity of the synthesized molecular salts/cocrystals. It was found that the FLC–2,3HBA salt, and the FLC–GAA and FLC–GLA cocrystals did not experience any hydration under the accelerated humidity conditions (both 70–75% RH and 90–95% RH) at ambient temperature (∼30 °C). However, FLC–2,6HBA and FLC–3,5HBA were found to be hygroscopic under 70–75% RH conditions. Furthermore, all the synthesized salts/cocrystals except FLC–3,5HBA were found to be stable for 2 months under ambient conditions (∼30 °C, 60–65% RH). Therefore, the FLC–2,3HBA salt, and the FLC–GAA and FLC–GLA cocrystals are better candidates for the preparation of new drug products of FLC.

Anticancer activity of complexes of the third row transition metals, rhenium, osmium, and iridium

Abstract: The clinical success of the platinum-based chemotherapeutic agents has prompted the investigation of coordination and organometallic complexes of alternative metal centers for use as anticancer agents. Among these alternatives, the third row transition metal neighbors of platinum on the periodic table have only recently been explored for their potential to yield anticancer-active complexes. In this Perspective, we summarize developments within the last six years on the application of rhenium, osmium, and iridium complexes as anticancer drug candidates. This review focuses on studies that discuss the potential mechanisms of action of these complexes. As reflected in this Perspective, complexes of these metal ions induce cancer cell death via a diverse range of mechanisms. Notably, small structural changes can significantly alter the mode of cell death, hindering efforts to elucidate structure–activity relationships. This property may both benefit and hinder the clinical development of these compounds.

Study of Composition and Morphology of Cadmium Oxide (Cdo) Nanoparticles for Eliminating Cancer Cells

Abstract: The effects of substrate temperature on the structural, optical, medical and electrical characteristics of Cadmium Oxide (CdO) films are investigated in the current study. Films are deposited on glass substrate at different temperatures, ranged between 450–600 oC, using Spray Pyrolysis Technique. According to X–Ray Diffraction (XRD), it is found that the films are polycrystalline and Cadmium Oxide (CdO) is of a hexagonal wurtzite structure which the preferred direction of its crystal plane is (002). The maximum optical transmittance of films is more than 85%. The size of crystallites is calculated with the maximum value in 500o C. Furthermore, Cadmium Oxide (CdO) nanoparticles were synthesized in deionized water by laser ablation of Cadmium plate. In the current paper, the effects of laser pulse energy and wavelength on the characteristics of Cadmium Oxide (CdO) nanoparticles were studied. Analyses of Transmission Electron Microscope (TEM) were confirmed that size distribution of Cadmium Oxide (CdO) nanoparticles is reduced by increase in laser pulse energy. Fluorescence spectrum of Cadmium Oxide (CdO) nanoparticles shows violet emission accompanied by blue and green band. UV emission with high intensity shows that nanostructure of Cadmium Oxide (CdO) is of a little deficiency. Also, the current study aims to study the linear and non–linear optical characteristics of Cadmium Oxide (CdO) nanoparticles and their applications. Firstly, fluorescence spectrum, as a linear characteristics of Cadmium Oxide (CdO), as well as second harmonic generation and two photons absorption, as non–linear characteristics of Cadmium Oxide (CdO), are studied. Then, some aspects of medicinal and pharmaceutical applications of Cadmium Oxide (CdO) nanoparticles for eliminating cancer cells such as the effect of Cadmium Oxide (CdO) nanoparticles on DNA of human cancer cells and the interaction of Cadmium Oxide (CdO) nanoparticles with DNA of cancer cells are originally investigated. It should be noted that the range of considered parameters are separately clarified and explained in each of related sections (Figure 1).

Synthesis, characterization, molecular docking and biological activities of novel pyrazoline derivatives.

Abstract: In this study, synthesis of ethyl 2-((4-bromophenyl)diazenyl)-3-oxo-phenylpropanoate 1 was carried out and a series of new 3H-pyrazol-3-ones (P1-7) were synthesized from 1 as well as various hydrazines. The obtained yields of the synthesized compounds were moderate (40-70%) and these compounds were confirmed by spectral data. These novel pyrazoline derivatives were effective inhibitor compounds of the human carbonic anhydrase I and II isozymes (hCAs I and II) and of the acetylcholinesterase (AChE) enzyme, with Ki values in the range of 17.4-40.7 nM for hCA I, 16.1-55.2 nM for hCA II, and 48.2-84.1 nM for AChE. In silico studies were performed on the compounds inhibiting hCA I, hCA II, and AChE receptors. On the basis of the findings, the inhibition profile of the new pyrazoline compounds at the receptors was determined.