Synthesis, characterization, DFT studies and evaluation of the potential anti-tumour activity of nicotinic hydrazide based Schiff base using in vitro and molecular …

V Preethi, VG Vijukumar, S AnilaRaj, VG Vidya - Heliyon, 2024 - cell.com
Breast cancer, one of the most serious issues worldwide, has been raising day by day. It has
now become a necessary to develop a suitable drug to combat this terrible illness. Schiff …

Experimental, spectroscopic, and theoretical investigation on structural and anticancer activities of Schiff bases derived from isonicotinohydrazide

S Gupta, SK Pandey, S Kumar, RN Gautam… - Journal of Molecular …, 2023 - Elsevier
Isoniazid hydrazones are promising possibilities as medicines since they have preserved
efficacy and are less toxic and resistant to resistance than parent Isoniazid (INH). Here, we …

In-silico molecular docking, ADMET and DFT evaluation of piperidin-4-one furoic hydrazone derivatives as antimicrobial, antioxidant and anticancer agents

M Sivanandhan, U Seeman, A Parasuraman - Journal of the Iranian …, 2024 - Springer
Abstract A series of N'-(2, 6-diarylpiperidin-4-ylidene) furan-2-carbohydrazide were
synthesized by incorporating hydrazide group in piperidine moiety and characterized by IR …

Quantum computational, spectroscopic investigation, molecular docking, and in vitro pharmacological studies of sulfonamide Schiff base

S Paul, MA Alam, TK Pal, MN Uddin, MM Islam… - Journal of Molecular …, 2022 - Elsevier
A new Schiff base,(E)-4-((3, 5-dibromo-2-hydroxybenzylidene) amino)-N-(5-methylisoxazol-
3-yl) benzenesulfonamide was synthesized and characterized by various physico-chemical …

A New Schiff Base Molecule Prepared from Pyrimidine-2-thione: Synthesis, Spectral Characterization, Cytotoxic Activity, DFT, and Molecular Docking Studies

Z KÖKBUDAK, B TÜRKMENOĞLU… - … University Journal of …, 2022 - dergipark.org.tr
Schiff base derivatives are some of the most widely used organic compounds for industrial
purposes and they exhibit a broad range of biological activities. In this paper, a new Schiff …

Synthesis, characterization, anti-proliferative activity and chemistry computation of DFT theoretical methods of hydrazine-based Schiff bases derived from methyl …

S Parvarinezhad, M Salehi - Journal of Molecular Structure, 2021 - Elsevier
In this study, the synthesized hydrazine Schiff bases belonging to methyl acetoacetate (1)
and α-hydroxyacetophenone (2) were prepared by simple methods. In addition, FT-IR, UV …

Synthesis, characterization, and biological properties of novel Schiff bases containing pentafluorophenyl hydrazine

F Hamurcu - Journal of Biochemical and Molecular Toxicology, 2023 - Wiley Online Library
In the present study, new Schiff bases derived from pentafluorophenyl‐hydrazine (L1, L2,
L3, L4) were synthesized and their structures were characterized by 1H nuclear magnetic …

Design, synthesis, anti-proliferative, anti-microbial, anti-angiogenic activity and in silico analysis of novel hydrazone derivatives

H Ünver, B Berber, R Demirel… - Anti-Cancer Agents in …, 2019 - ingentaconnect.com
Background: Cancer is the second leading cause of death globally. Hydrazone and
hydrazone derivatives have high activity, and for this reason, these compound are greatly …

Synthesis, structure–activity relationship studies using density functional theory and in silico molecular docking on substituted benzohydrazide derivatives

PM Gurubasavaraj, VP Sajjan, BM Muñoz-Flores… - Journal of Molecular …, 2024 - Elsevier
The present study demonstrates the utility of benzohydrazide derivatives based on an
approach to identify potential targets for a series of synthesized compounds that show potent …

Schiff base (Z)-4-((furan-2-ylmethylene) amino) benzenesulfonamide: synthesis, solvent interactions through hydrogen bond, structural and spectral properties …

S Manivel, BS Gangadharappa, N Elangovan… - Journal of Molecular …, 2022 - Elsevier
A new Schiff base (Z)-4-((furan-2-ylmethylene) amino) benzenesulfonamide (FURNI) was
synthesized by the reaction reaction between furfural and sulfanilamide followed by …