Thiazolidine-2, 4-diones: Progress towards multifarious applications
VS Jain, DK Vora, CS Ramaa - Bioorganic & medicinal chemistry, 2013 - Elsevier
The promising activity shown by compounds containing thiazolidine-2, 4-dione nucleus in
numerous categories such as anti-hyperglycaemics, aldose reductase inhibitors, anti …
numerous categories such as anti-hyperglycaemics, aldose reductase inhibitors, anti …
Thiazolidin-2, 4-dione scaffold: an insight into recent advances as antimicrobial, antioxidant, and hypoglycemic agents
Heterocyclic compounds containing nitrogen and sulfur, especially those in the thiazole
family, have generated special interest in terms of their synthetic chemistry, which is …
family, have generated special interest in terms of their synthetic chemistry, which is …
Novel hybrids of thiazolidinedione-1, 3, 4-oxadiazole derivatives: synthesis, molecular docking, MD simulations, ADMET study, in vitro, and in vivo anti-diabetic …
MG Srinivasa, JG Paithankar, SRS Birangal, A Pai… - RSC …, 2023 - pubs.rsc.org
As compared to standard medicinal compounds, hybrid molecules that contain multiple
biologically active functional groups have greater affinity and efficiency. Hence based on this …
biologically active functional groups have greater affinity and efficiency. Hence based on this …
Antifungal thiazolidines: Synthesis and biological evaluation of mycosidine congeners
IB Levshin, AY Simonov, SN Lavrenov, AA Panov… - Pharmaceuticals, 2022 - mdpi.com
Novel derivatives of Mycosidine (3, 5-substituted thiazolidine-2, 4-diones) are synthesized
by Knoevenagel condensation and reactions of thiazolidines with chloroformates or halo …
by Knoevenagel condensation and reactions of thiazolidines with chloroformates or halo …
Antibacterial properties of 5-substituted derivatives of rhodanine-3-carboxyalkyl acids
A series of rhodanine 3-carboxyalkanoic acid derivatives possessing 4′-(N, N-dialkyl-
amino or diphenylamino)-benzylidene moiety as a substituent at the C-5 position were …
amino or diphenylamino)-benzylidene moiety as a substituent at the C-5 position were …
Novel tetrazoloquinoline–rhodanine conjugates: highly efficient synthesis and biological evaluation
In search of new active molecules against Mycobacterium tuberculosis (MTB) H37Ra and
Mycobacterium bovis BCG, a small focused library of rhodanine incorporated …
Mycobacterium bovis BCG, a small focused library of rhodanine incorporated …
Evaluation of thiazolidinone derivatives as a new class of mushroom tyrosinase inhibitors
M Rezaei, HT Mohammadi, A Mahdavi… - International journal of …, 2018 - Elsevier
Abstract Tyrosinase (EC 1.14. 18.1) is a key copper-containing metalloenzyme widely
distributed in nature and plays determinant role in melanin biosynthesis. The enzyme …
distributed in nature and plays determinant role in melanin biosynthesis. The enzyme …
[HTML][HTML] Synthesis and antibacterial activity of new (2, 4-dioxothiazolidin-5-yl/ylidene) acetic acid derivatives with thiazolidine-2, 4-dione, rhodanine and 2 …
N Trotsko, U Kosikowska, A Paneth, M Wujec… - Saudi pharmaceutical …, 2018 - Elsevier
Abstract A series of new (2, 4-dioxothiazolidin-5-yl/ylidene) acetic acid derivatives with
thiazolidine-2, 4-dione, rhodanine and 2-thiohydantoin moiety (28–65) were synthesized by …
thiazolidine-2, 4-dione, rhodanine and 2-thiohydantoin moiety (28–65) were synthesized by …
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 …
reusable DBU acetate as ionic liquid and evaluated for their in vitro antitubercular activity …
Synthesis and biological evaluation of new rhodanine analogues bearing 2-chloroquinoline and benzo [h] quinoline scaffolds as anticancer agents
Abstract Several rhodanine derivatives (9–39) were synthesized for evaluation of their
potential as anticancer agents. Villsmeier cyclization to synthesize aza-aromatic aldehydes …
potential as anticancer agents. Villsmeier cyclization to synthesize aza-aromatic aldehydes …