Recent developments with rhodanine as a scaffold for drug discovery

D Kaminskyy, A Kryshchyshyn… - Expert Opinion on Drug …, 2017 - Taylor & Francis
Introduction: Rhodanines, as one of the 4-thiazolidinones subtypes, are recognized as
privileged heterocycles in medicinal chemistry. The main achievements include the …

Antitubercular properties of thiazolidin-4-ones–A review

N Trotsko - European Journal of Medicinal Chemistry, 2021 - Elsevier
Thiazolidin-4-one scaffold has great potential for medicinal chemistry and is of interest to
scientists in view of wide spectrum of biological activity. This scaffold is often used for …

Opportunities for Overcoming Mycobacterium tuberculosis Drug Resistance: Emerging Mycobacterial Targets and Host-Directed Therapy

E Torfs, T Piller, P Cos, D Cappoen - International journal of molecular …, 2019 - mdpi.com
The ever-increasing incidence of drug-resistant Mycobacterium tuberculosis infections has
invigorated the focus on the discovery and development of novel treatment options. The …

Chemical, computational and functional insights into the chemical stability of the Hedgehog pathway inhibitor GANT61

A Calcaterra, V Iovine, B Botta, D Quaglio… - Journal of enzyme …, 2018 - Taylor & Francis
This work aims at elucidating the mechanism and kinetics of hydrolysis of GANT61, the first
and most-widely used inhibitor of the Hedgehog (Hh) signalling pathway that targets Glioma …

Novel tetrazoloquinoline–rhodanine conjugates: highly efficient synthesis and biological evaluation

DD Subhedar, MH Shaikh, L Nawale, A Yeware… - Bioorganic & Medicinal …, 2016 - Elsevier
In search of new active molecules against Mycobacterium tuberculosis (MTB) H37Ra and
Mycobacterium bovis BCG, a small focused library of rhodanine incorporated …

Quinolidene-rhodanine conjugates: Facile synthesis and biological evaluation

DD Subhedar, MH Shaikh, BB Shingate… - European Journal of …, 2017 - Elsevier
A series of rhodanine incorporated quinoline derivatives were efficiently synthesized using
reusable DBU acetate as ionic liquid and evaluated for their in vitro antitubercular activity …

Deletion of zmp1 improves Mycobacterium bovis BCG-mediated protection in a guinea pig model of tuberculosis

P Sander, S Clark, A Petrera, C Vilaplana, M Meuli… - Vaccine, 2015 - Elsevier
Having demonstrated previously that deletion of zinc metalloprotease zmp1 in
Mycobacterium bovis BCG increased immunogenicity of BCG vaccines, we here …

Development of Potent Inhibitors of the Mycobacterium tuberculosis Virulence Factor Zmp1 and Evaluation of Their Effect on Mycobacterial Survival inside …

M Paolino, M Brindisi, A Vallone, S Butini… - …, 2018 - Wiley Online Library
The enzyme Zmp1 is a zinc‐containing peptidase that plays a critical role in the
pathogenicity of Mycobacterium tuberculosis. Herein we describe the identification of a small …

Mycobacterium tuberculosis Molecular Determinants of Infection, Survival Strategies, and Vulnerable Targets

DM Ferraris, R Miggiano, F Rossi, M Rizzi - Pathogens, 2018 - mdpi.com
Mycobacterium tuberculosis is the causative agent of tuberculosis, an ancient disease
which, still today, represents a major threat for the world population. Despite the advances in …

[Et3NH][HSO4] catalyzed efficient synthesis of 5-arylidene-rhodanine conjugates and their antitubercular activity

DD Subhedar, MH Shaikh, L Nawale, A Yeware… - Research on chemical …, 2016 - Springer
We have described a highly efficient, safer protocol for the synthesis of 5-arylidene-
rhodanine conjugates catalyzed by Bronsted acidic ionic liquid [Et 3 NH][HSO 4] in excellent …