[HTML][HTML] Schiff bases: A short review of their antimicrobial activities
CM Da Silva, DL da Silva, LV Modolo, RB Alves… - Journal of Advanced …, 2011 - Elsevier
Schiff bases are aldehyde-or ketone-like compounds in which the carbonyl group is
replaced by an imine or azomethine group. They are widely used for industrial purposes and …
replaced by an imine or azomethine group. They are widely used for industrial purposes and …
Visible light photocatalysis in the synthesis of pharmaceutically relevant heterocyclic scaffolds
Visible light and photoredox catalysis have emerged as a powerful and long-lasting tool for
organic synthesis, demonstrating the importance of a variety of chemical bond formation …
organic synthesis, demonstrating the importance of a variety of chemical bond formation …
Promising Schiff bases in antiviral drug design and discovery
Emerging and re-emerging illnesses will probably present a new hazard of infectious
diseases and have fostered the urge to research new antiviral agents. Most of the antiviral …
diseases and have fostered the urge to research new antiviral agents. Most of the antiviral …
Exploring the antibacterial activity of 1, 2 diaminoethane hexanedionic acid by spectroscopic, electronic, ELF, LOL, RDG analysis and molecular docking studies using …
CD Vincy, JDD Tarika, XDD Dexlin, A Rathika… - Journal of Molecular …, 2022 - Elsevier
Diaminoethane hexanedionic acid, selected for its antibacterial property is extensively used
for spectroscopic elucidations and computational aspects using density functional methods …
for spectroscopic elucidations and computational aspects using density functional methods …
Synthesis, antibacterial, antifungal and antiviral activity evaluation of some new bis-Schiff bases of isatin and their derivatives
A Jarrahpour, D Khalili, E De Clercq, C Salmi… - Molecules, 2007 - mdpi.com
Twelve new bis-Schiff bases of isatin, benzylisatin and 5-fluoroisatin 3a-3l were prepared by
condensation of isatin, benzylisatin and 5-fluoroisatin with primary aromatic amines. The …
condensation of isatin, benzylisatin and 5-fluoroisatin with primary aromatic amines. The …
Thiosemicarbazones from the old to new: iron chelators that are more than just ribonucleotide reductase inhibitors
Y Yu, DS Kalinowski, Z Kovacevic… - Journal of medicinal …, 2009 - ACS Publications
The chemical and biological effects of thiosemicarbazones have received considerable
interest from medicinal chemists for many years. This is attributed to, first, their wide …
interest from medicinal chemists for many years. This is attributed to, first, their wide …
Isatin containing heterocycles for different biological activities: Analysis of structure activity relationship
R Nath, S Pathania, G Grover, MJ Akhtar - Journal of Molecular Structure, 2020 - Elsevier
Isatin has been widely used in drug discovery. The ring is part of many naturally occurring
compounds and is used to design compounds with diverse biological activities. These isatin …
compounds and is used to design compounds with diverse biological activities. These isatin …
[PDF][PDF] Biological activities of isatin and its derivatives
SN Pandeya, S Smitha, M Jyoti, SK Sridhar - Acta Pharm, 2005 - Citeseer
Isatin is an endogenous compound identified in humans that possesses a wide range of
biological activities. Isatin has anxiogenic, sedative, anticonvulsant activities and acts as a …
biological activities. Isatin has anxiogenic, sedative, anticonvulsant activities and acts as a …
Synthesis and antimicrobial activities of Schiff bases derived from 5-chloro-salicylaldehyde
L Shi, HM Ge, SH Tan, HQ Li, YC Song, HL Zhu… - European journal of …, 2007 - Elsevier
A series of Schiff bases (compounds 1–26) were synthesized by reacting 5-chloro-
salicylaldehyde and primary amines, 15 (compounds 2–4, 6, 7, 10, 12–17, 23, 25 and 26) of …
salicylaldehyde and primary amines, 15 (compounds 2–4, 6, 7, 10, 12–17, 23, 25 and 26) of …
Synthesis, characterization and biological activity of Schiff base analogues of indole-3-carboxaldehyde
Eight novel heterocyclic Schiff bases derived from the condensation reactions of indole 3-
carboxaldehyde with different l-amino acids (histidine, glutamic acid, aspartic acid, leucine …
carboxaldehyde with different l-amino acids (histidine, glutamic acid, aspartic acid, leucine …