[HTML][HTML] Anti-tuberculosis Mur inhibitors: structural insights and the way ahead for development of novel agents

K Mehta, M Khambete, A Abhyankar, A Omri - Pharmaceuticals, 2023 - mdpi.com
Mur enzymes serve as critical molecular devices for the synthesis of UDP-MurNAc-
pentapeptide, the main building block of bacterial peptidoglycan polymer. These enzymes …

Characterization, quantification and a multi-computational in silico toxicity assessment of impurity (feruloyl methane) in synthetic curcumin using RP-HPLC-UV …

RS Nunavath, KC Bhadram, K Nagappan - Journal of pharmaceutical and …, 2023 - Elsevier
Feruloyl Methane (FM) is a common impurity in Synthetic Curcumin (SC) that affects its purity
and potency. The identification and quantification of FM is crucial to ensure the quality and …

[HTML][HTML] 5-benzyliden-2-(5-methylthiazol-2-ylimino) thiazolidin-4-ones as antimicrobial agents. design, synthesis, biological evaluation and molecular docking studies

M Haroun, C Tratrat, A Kolokotroni, A Petrou… - Antibiotics, 2021 - mdpi.com
In this study, we report the design, synthesis, computational and experimental evaluation of
the antimicrobial activity, as well as docking studies of new 5-methylthiazole based …

Discovery of benzothiazole-based thiazolidinones as potential anti-inflammatory agents: Anti-inflammatory activity, soybean lipoxygenase inhibition effect and …

M Haroun, A Petrou, C Tratrat, K Kositsi… - SAR and QSAR in …, 2022 - Taylor & Francis
Despite the greatest achievement in the development of anti-inflammatory agents in the last
two decades, the current clinical drugs suffer from a variety of complications in community …

2-Aryl-3-(6-trifluoromethoxy) benzo [d] thiazole-based thiazolidinone hybrids as potential anti-infective agents: Synthesis, biological evaluation and molecular docking …

M Haroun, C Tratrat, A Petrou, A Geronikaki… - Bioorganic & Medicinal …, 2021 - Elsevier
The search for new antimicrobial agents is greater than ever due to the perpetual threat of
multidrug resistance in known pathogens and the relentless emergence of new infections. In …

Benzothiazole as a promising scaffold for the development of antifungal agents

C Tratrat - Current Topics in Medicinal Chemistry, 2023 - ingentaconnect.com
Despite great efforts in the discovery of antifungal drugs in the last two decades, the
increasing incidence of infectious diseases from diverse pathogenic fungi threatens public …

[HTML][HTML] 1, 2, 3-Triazolyl-tetrahydropyrimidine conjugates as potential sterol carrier protein-2 inhibitors: Larvicidal activity against the malaria vector anopheles …

KN Venugopala, P Shinu, C Tratrat, PK Deb… - Molecules, 2022 - mdpi.com
Alteration of insect growth regulators by the action of inhibitors is becoming an attractive
strategy to combat disease-transmitting insects. In the present study, we investigated the …

Synthesis, biological evaluation, and computational investigation of ethyl 2, 4, 6-trisubstituted-1, 4-dihydropyrimidine-5-carboxylates as potential larvicidal agents …

R Duraisamy, NA Al-Shar'i… - Journal of …, 2024 - Taylor & Francis
Malaria is one of the most known vector-borne diseases caused by female Anopheles
mosquito bites. According to WHO, about 247 million cases of malaria and 619,000 deaths …

[HTML][HTML] Identification of novel cyclooxygenase-1 selective inhibitors of thiadiazole-based scaffold as potent anti-inflammatory agents with safety gastric and cytotoxic …

M Haroun, M Fesatidou, A Petrou, C Tratrat… - Molecules, 2023 - mdpi.com
Major obstacles faced by the use of nonsteroidal anti-inflammatory drugs (NSAID) are their
gastrointestinal toxicity induced by non-selective inhibition of both cyclooxygenases (COX) 1 …

4-Aryl-1, 4-dihydropyridines as potential enoyl-acyl carrier protein reductase inhibitors: antitubercular activity and molecular docking study

KN Venugopala, PK Deb, M Pillay… - Current Topics in …, 2021 - ingentaconnect.com
Background: Tuberculosis remains one of the most deadly infectious diseases worldwide
due to the emergence of multi-drug resistance (MDR) and extensively drug resistance (XDR) …