Recent advances of imidazole-containing derivatives as anti-tubercular agents

YL Fan, XH Jin, ZP Huang, HF Yu, ZG Zeng… - European journal of …, 2018 - Elsevier
Tuberculosis still remains one of the most common, communicable, and leading deadliest
diseases known to mankind throughout the world. Drug-resistance in Mycobacterium …

Novel benzothiazole-based dual VEGFR-2/EGFR inhibitors targeting breast and liver cancers: Synthesis, cytotoxic activity, QSAR and molecular docking studies

EA Abd El-Meguid, AM Naglah, GO Moustafa… - Bioorganic & Medicinal …, 2022 - Elsevier
A novel series of benzothiazole-based derivatives linked to various amino acids and their
corresponding ethyl ester analogues were prepared and were initially evaluated for their …

Treating Hyperglycemia From Eryngium caeruleum M. Bieb: In-vitro α-Glucosidase, Antioxidant, in-vivo Antidiabetic and Molecular Docking-Based Approaches

A Sadiq, U Rashid, S Ahmad, M Zahoor… - Frontiers in …, 2020 - frontiersin.org
Natural-based drugs are believed to be safe, effective and economical. Based on the
medicinal importance of the genus Eryngium and unexplored nature of Eryngium …

Tailoring the substitution pattern of Pyrrolidine-2, 5-dione for discovery of new structural template for dual COX/LOX inhibition

A Sadiq, MH Mahnashi, BA Alyami, YS Alqahtani… - Bioorganic …, 2021 - Elsevier
Dual inhibition of the enzymatic pathways of cyclooxygenases (COX-1/COX-2) and
lipoxygenase (LOX) is a rational approach for developing more efficient and safe anti …

Emerging target-directed approaches for the treatment and diagnosis of microbial infections

MC Almeida, PM da Costa, E Sousa… - Journal of Medicinal …, 2022 - ACS Publications
With the rising levels of drug resistance, developing efficient antimicrobial therapies has
become a priority. A promising strategy is the conjugation of antibiotics with relevant …

Design and Synthesis of Imidazo/Benzimidazo[1,2-c]quinazoline Derivatives and Evaluation of Their Antimicrobial Activity

NK Nandwana, RP Singh, OPS Patel, S Dhiman… - ACS …, 2018 - ACS Publications
A new class of fused quinazolines has been designed and synthesized via copper-catalyzed
Ullmann type C–N coupling followed by intramolecular cross-dehydrogenative coupling …

Synthetic and pharmacological developments in the hybrid s-triazine moiety: A review

D Bareth, S Jain, J Kumawat, D Kishore, J Dwivedi… - Bioorganic …, 2024 - Elsevier
This article summarizes the most recent advancements in the synthetic and pharmacological
approaches along with the structure activity relationship towards the s-triazine and its …

Synthesis and in vitro urease inhibitory activity of 5-nitrofuran-2-yl-thiadiazole linked to different cyclohexyl-2-(phenylamino) acetamides, in silico and kinetic studies

M Asadi, A Iraji, M Sherafati, MN Montazer, S Ansari… - Bioorganic …, 2022 - Elsevier
Abstract A series of 5-nitrofuran-2-yl-thiadiazole linked to different cyclohexyl-2-
(phenylamino) acetamides were rationally designed and synthesized. All synthetic …

Metronidazole-conjugates: A comprehensive review of recent developments towards synthesis and medicinal perspective

OPS Patel, OJ Jesumoroti, LJ Legoabe… - European Journal of …, 2021 - Elsevier
Nitroimidazoles based compounds remain a hot topic of research in medicinal chemistry
due to their numerous biological activities. Moreover, many clinical candidates based on this …

Exploring the ability of dihydropyrimidine-5-carboxamide and 5-benzyl-2, 4-diaminopyrimidine-based analogues for the selective inhibition of L. major Dihydrofolate …

M Bibi, NA Qureshi, A Sadiq, U Farooq… - European Journal of …, 2021 - Elsevier
To tackle leishmaniasis, search for efficient therapeutic drug targets should be pursued.
Dihydrofolate reductase (DHFR) is considered as a key target for the treatment of …