Synthesis and biological activity of 1, 3, 4-oxadiazoles used in medicine and agriculture

M Luczynski, A Kudelko - Applied Sciences, 2022 - mdpi.com
Biologically active compounds play a key role in the fight against diseases affecting both
human and animal living organisms, as well as plants. Finding out about new molecules …

Oxadiazole: A highly versatile scaffold in drug discovery

N Desai, J Monapara, A Jethawa… - Archiv der …, 2022 - Wiley Online Library
As a pharmacologically important heterocycle, oxadiazole paved the way to combat the
problem associated with the confluence of many commercially available drugs with different …

Investigation of novel benzoxazole-oxadiazole derivatives as effective anti-Alzheimer's agents: in vitro and in silico approaches

S Anwar, W Rehman, R Hussain, S Khan, MM Alanazi… - Pharmaceuticals, 2023 - mdpi.com
Alzheimer's disease (AD) is a progressive neurological illness that is distinguished clinically
by cognitive and memory decline and adversely affects the people of old age. The …

Therapeutic potential of oxadiazole or furadiazole containing compounds

A Siwach, PK Verma - BMC chemistry, 2020 - Springer
As we know that, Oxadiazole or furadi azole ring containing derivatives are an important
class of heterocyclic compounds. A heterocyclic five-membered ring that possesses two …

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 …

Comparative study of the synthetic approaches and biological activities of the bioisosteres of 1, 3, 4-oxadiazoles and 1, 3, 4-thiadiazoles over the past decade

RM El-Masry, HH Kadry, AT Taher, SM Abou-Seri - Molecules, 2022 - mdpi.com
The bioisosteres of 1, 3, 4-oxadiazoles and 1, 3, 4-thiadiazoles are well-known
pharmacophores for many medicinally important drugs. Throughout the past 10 years, 1, 3, 4 …

New Arene and/or Heteroarene‐Linked 1, 3, 4‐Oxadiazoles: Synthesis of Potential Methicillin‐Resistant Staphylococcus aureus and Vancomycin‐Resistant …

AEM Mekky, RA Abdelbaath, RA Abdelbaath… - …, 2024 - Wiley Online Library
Bacterial infections, particularly those associated with methicillin‐resistant Staphylococcus
aureus (MRSA) and vancomycin‐resistant Enterococcus (VRE), threaten public health and …

Identification of Novel β-Tubulin Inhibitors Using a Combined In Silico/In Vitro Approach

MJ Horgan, L Zell, B Siewert, H Stuppner… - Journal of Chemical …, 2023 - ACS Publications
Due to their potential as leads for various therapeutic applications, including as antimitotic
and antiparasitic agents, the development of tubulin inhibitors offers promise for drug …

Tandem synthesis, antibacterial evaluation and SwissADME prediction study of new bis (1, 3, 4-oxadiazoles) linked to arene units

AEM Mekky, SMH Sanad, AM Abdelfattah - Mendeleev Communications, 2022 - Elsevier
A three-component tandem protocol involving the reactions of bis (benzohydrazides),
aromatic aldehydes and chloramine trihydrate yielded a new series of bis (1, 3, 4 …

Tubulin inhibitors binding to colchicine-site: a review from 2015 to 2019

LY **a, YL Zhang, R Yang, ZC Wang… - Current medicinal …, 2020 - ingentaconnect.com
Due to the three domains of the colchicine-site which is conducive to the combination with
small molecule compounds, colchicine-site on the tubulin has become a common target for …