Synthesis, spectroscopic, in-vitro and computational analysis of hydrazones as potential antituberculosis agents:(part-I)

BR Thorat, D Rani, RS Yamgar… - … Chemistry & High …, 2020 - ingentaconnect.com
Background: Since the last few decades, the healthcare sector is facing the problem of the
development of multidrug-resistant (MDR-TB) and extensively drug-resistant tuberculosis …

Novel Therapies for Biofilm-Based Candida spp. Infections

L Černáková, C Light, B Salehi… - … Infectious Diseases and …, 2019 - Springer
The presence of fungal infections continue to grow worldwide, mostly in immunosuppressed
patients, and in individuals with continued antimicrobial treatments. Candida spp. are the …

Synthesis and anti-mycobacterium study on halo-substituted 2-aryl oxyacetohydrazones

VJ Desale, SN Mali, HK Chaudhari… - … computer-aided drug …, 2020 - ingentaconnect.com
Background: The treatment of multiple-drug-resistant tuberculosis (MDR-TB) with currently
available marketed drugs remains a global health concern. The cases of resistant …

Synthesis, structures and urease inhibitory activity of cobalt (III) complexes with Schiff bases

C Jing, C Wang, K Yan, K Zhao, G Sheng, D Qu… - Bioorganic & Medicinal …, 2016 - Elsevier
A series of new cobalt (III) complexes were prepared. They are [CoL 1 (py) 3]· NO 3 (1),[CoL
2 (bipy)(N 3)]· CH 3 OH (2),[CoL 3 (HL 3)(N 3)]· NO 3 (3), and [CoL 4 (MeOH)(N 3)](4), where …

[HTML][HTML] Hybrid Inorganic Complexes as Cancer Therapeutic Agents: In-vitro Validation

MA Betallu, SR Bhalara, KB Sapnar, VB Tadke… - …, 2023 - ncbi.nlm.nih.gov
A series of novel mixed transition metal-Magnesium tartarate complexes of general
formulation [MMg (C 4 H 4 O 6) 2. xH 2 O](where M= Mn, Fe, Co, Ni, Cu and Zn) is prepared …

Substituent effect in salicylaldehyde 2-furoic acid hydrazones: Theoretical and experimental insights into DNA/BSA affinity modulation, antimicrobial and antioxidant …

A Zahirović, S Fetahović, M Feizi-Dehnayebi… - Journal of molecular …, 2024 - Elsevier
The biological properties of five aroylhydrazones derived from salicylaldehyde and its 5-
substituted derivatives with 2-furoic acid hydrazide were thoroughly investigated. NMR …

[HTML][HTML] Novel Orally Active Analgesic and Anti-Inflammatory Cyclohexyl-N-Acylhydrazone Derivatives

TF Silva, W Bispo Junior, MS Alexandre-Moreira… - Molecules, 2015 - mdpi.com
The N-acylhydrazone (NAH) moiety is considered a privileged structure, being present in
many compounds with diverse pharmacological activities. Among the activities attributed to …

Benzimidazole-derived carbohydrazones as dual monoamine oxidases and acetylcholinesterase inhibitors: design, synthesis, and evaluation

S Kumar, S Jaiswal, SK Gupta… - Journal of Biomolecular …, 2023 - Taylor & Francis
A series of novel benzimidazole-derived carbohydrazones was designed, synthesized and
evaluated for their dual inhibition potential against monoamine oxidases (MAOs) and …

Properties, structure and stability of V (IV) hydrazide Schiff base ligand complex

R Gryboś, J Szklarzewicz, A Jurowska… - Journal of Molecular …, 2018 - Elsevier
The reaction of vanadyl sulfate, VOSO 4· H 2 O, with Schiff base ligand based on 2-
hydroxybenzhydrazide and 5-bromosalicylaldehyde, with addition of 1, 10-phenantroline as …

Synthesis, molecular docking, antioxidant, anti-TB, and potent MCF-7 anticancer studies of novel aryl-carbohydrazide analogues

BR Thorat, SN Mali, RR Wagh… - … Computer-Aided Drug …, 2022 - ingentaconnect.com
Background: Hydrazide-hydrazone-based compounds are reported for their wider
pharmacological potentials. Methods: In the present work, we synthesized 10 new Schiff …