1, 3, 4‐oxadiazole and its derivatives: A review on recent progress in anticancer activities

A Vaidya, D Pathak, K Shah - Chemical biology & drug design, 2021 - Wiley Online Library
Abstract The 1, 3, 4‐oxadiazole nucleus is a biologically imperative scaffold possesses
numerous biological activities. The broad and potent activity of 1, 3, 4‐oxadiazole and their …

A review of the biological activities of heterocyclic compounds comprising oxadiazole moieties

BF Ruan, QL Guo, QS Li, LZ Li… - Current Topics in …, 2022 - ingentaconnect.com
The oxadiazole core is considered a privileged moiety in many medicinal chemistry
applications. The oxadiazole class includes 1, 2, 3-oxadiazole, 1, 2, 4-oxadiazole, 1, 3, 4 …

Novel hybrids of benzothiazole-1, 3, 4-oxadiazole-4-thiazolidinone: Synthesis, in silico ADME study, molecular docking and in vivo anti-diabetic assessment

R Bhutani, DP Pathak, G Kapoor, A Husain… - Bioorganic chemistry, 2019 - Elsevier
A series of new benzothiazole-1, 3, 4-oxadiazole-4-thiazolidinone hybrid analogs (Tz1-
Tz28) were synthesized in search of potential anti-diabetic agents. Molecular docking study …

Identification of 1, 3, 4-oxadiazoles as tubulin-targeted anticancer agents: a combined field-based 3D-QSAR, pharmacophore model-based virtual screening …

A Das, M Sarangi, K Jangid, V Kumar… - Journal of …, 2024 - Taylor & Francis
Cancer is one of the most prominent causes of death worldwide and tubulin is a crucial
protein of cytoskeleton that maintains essential cellular functions including cell division as …

Design, synthesis, and biological evaluation of chalcone-linked thiazole-imidazopyridine derivatives as anticancer agents

VR Suma, R Sreenivasulu, MVB Rao… - Medicinal Chemistry …, 2020 - Springer
A novel library of chalcone linked thiazole-imidazopyridine (12a–j) derivatives were
designed, synthesized, and their structures were characterized by 1 H NMR, 13 C NMR and …

Synthesis, anticancer evaluation and molecular docking studies of 2, 5-bis (indolyl)-1, 3, 4-oxadiazoles, Nortopsentin analogues

R Sreenivasulu, MB Tej, SS Jadav, P Sujitha… - Journal of Molecular …, 2020 - Elsevier
A series of ten novel 2, 5-bis (indolyl)-1, 3, 4-oxadiazoles were designed and synthesized.
All these compounds were evaluated for their cytotoxicity against four cancer cell lines …

Design, synthesis, and biological evaluation of 1, 2, 4-thiadiazole-1, 2, 4-triazole derivatives bearing amide functionality as anticancer agents

YJ Pragathi, R Sreenivasulu, D Veronica… - Arabian journal for …, 2021 - Springer
A novel library of amide functionality having 1, 2, 4-thiadiazole-1, 2, 4-triazole (8a–j) analogs
was designed, synthesized, and structures were characterized by 1 H NMR, 13 C NMR, and …

Design, synthesis, anti-cancer evaluation and binding mode studies of benzimidazole/benzoxazole linked β-carboline derivatives

R Sireesha, R Sreenivasulu, C Chandrasekhar… - Journal of Molecular …, 2021 - Elsevier
A new series of benzimidazole/benzoxazole linked β-carbolines (9a-j) were rationally
designed and synthesized by combining two different anti-cancer fragments. The new hybrid …

Theoretical SERS study of the strength and suitability of Cu12 nanostar for SERS: Complete theoretical studies, coinage metal SM12 comparisons, benzothiazole …

JS Al-Otaibi, YS Mary, YS Mary, RK Trivedi… - Computational and …, 2022 - Elsevier
Theoretical calculations were used to optimize molecular structures which help determine
binding energies, and elucidate electronic properties of unsubstituted benzothiazole (BTH) …

Design, synthesis and anticancer evaluation of carbazole fused aminopyrimidine derivatives

Z Spandana, R Sreenivasulu… - Letters in Organic …, 2019 - ingentaconnect.com
Carbazole is an important type of tricyclic nitrogen containing compound and isolated first
from coal tar in 1872 by Graebe and Glazer. Carbazole alkaloids have received …