Has ferrocene really delivered its role in accentuating the bioactivity of organic scaffolds?

B Sharma, V Kumar - Journal of medicinal chemistry, 2021 - ACS Publications
Ferrocene is an important structural core in bioorganometallic chemistry because of its
inherent stability, excellent redox properties, and low toxicity. Ferroquine and ferrocifen are …

Ferrocene derivatives as anti-infective agents

BS Ludwig, JDG Correia, FE Kühn - Coordination Chemistry Reviews, 2019 - Elsevier
Infectious diseases like malaria, tuberculosis or HIV are among the leading causes of death
worldwide according to WHO estimations. Nevertheless, the fight against infectious diseases …

Recent advances in bioactive flavonoid hybrids linked by 1, 2, 3-triazole ring obtained by click chemistry

D Pereira, M Pinto, M Correia-da-Silva, H Cidade - Molecules, 2021 - mdpi.com
As a result of the biological activities of natural flavonoids, several synthetic strategies
aiming to obtain analogues with improved potency and/or pharmacokinetic profile have …

Anti-Tubercular Properties of 4-Amino-5-(4-Fluoro-3- Phenoxyphenyl)-4H-1,2,4-Triazole-3-Thiol and Its Schiff Bases: Computational Input and Molecular Dynamics

KN Venugopala, M Kandeel, M Pillay, PK Deb… - Antibiotics, 2020 - mdpi.com
In the present investigation, the parent compound 4-amino-5-(4-fluoro-3-phenoxyphenyl)-4
H-1, 2, 4-triazole-3-thiol (1) and its Schiff bases 2, 3, and 4 were subjected to whole-cell anti …

Multi-target polypharmacology of 4-aminoquinoline compounds against malaria, tuberculosis and cancer

S Nandi, B Chauhan, H Tarannum… - Current Topics in …, 2023 - benthamdirect.com
Background: Polypharmacology means drugs having interactions with multiple targets of a
unique disease or many disease pathways. This concept has been greatly appreciated …

Keto-bridged dual triazole-linked benzenesulfonamides as potent carbonic anhydrase and cathepsin B inhibitors

L Vats, P Arya, R Kumar, S Giovannuzzi… - Future Medicinal …, 2023 - Taylor & Francis
Background: Inhibition of human carbonic anhydrase (hCA) isoforms IX and XII with
concurrent inhibition of cathepsin B is a promising approach for targeting cancers …

Triazole-Containing Hybrids With Anti-Mycobacterium Tuberculosis Potential – Part I: 1,2,3-Triazole

Z Tan, J Deng, Q Ye, Z Zhang - Future Medicinal Chemistry, 2021 - Taylor & Francis
Tuberculosis regimens currently applied in clinical practice require months of multidrug
therapy, which imposes a major challenge of patient compliance and drug resistance …

Microwave-promoted facile access to 4-aminoquinoline-phthalimides: Synthesis and anti-plasmodial evaluation

A Rani, A Singh, J Gut, PJ Rosenthal… - European Journal of …, 2018 - Elsevier
Microwave promoted high yielding synthesis of 4-aminoquinoline-phthalimides was
developed with an aim to evaluate their anti-plasmodial potential. The scaffolds with longer …

Chalcones as anti-infective agents for effective management of tuberculosis

S Mishra, P Jana - Polycyclic Aromatic Compounds, 2024 - Taylor & Francis
After the pandemic COVID-19, global health agencies remind us that tuberculosis is the
deadliest infectious disease worldwide. As per WHO reports, approximately ten million …

New nucleic base-tethered trithiolato-bridged dinuclear ruthenium (II)-arene compounds: Synthesis and antiparasitic activity

O Desiatkina, M Mösching, N Anghel, G Boubaker… - Molecules, 2022 - mdpi.com
Aiming toward compounds with improved anti-Toxoplasma activity by exploiting the parasite
auxotrophies, a library of nucleobase-tethered trithiolato-bridged dinuclear ruthenium (II) …