Triazolothiadiazoles and triazolothiadiazines–Biologically attractive scaffolds

I Khan, A Ibrar, N Abbas - European Journal of Medicinal Chemistry, 2013 - Elsevier
Contemporary medicinal chemistry faces diverse challenges from several directions,
including the need for both potency and specificity of any therapeutic agent. Therefore, in the …

Synthesis, crystal structure and biological evaluation of some novel 1, 2, 4-triazolo [3, 4-b]-1, 3, 4-thiadiazoles and 1, 2, 4-triazolo [3, 4-b]-1, 3, 4-thiadiazines

I Khan, S Zaib, A Ibrar, NH Rama, J Simpson… - European journal of …, 2014 - Elsevier
Nitrogen-containing heterocycles are of particular interest and significant importance for the
discovery of potent bioactive agents in pharmaceutical industry. The present study reports …

Synthetic and biological aspects of thiadiazoles and their condensed derivatives: an overview

J Dwivedi, N Kaur, D Kishore, S Kumari… - Current Topics in …, 2016 - ingentaconnect.com
The three heteroatoms containing five membered heterocycles such as thiadiazoles have
been extensively studied due to their important pharmacological activities. The thiadiazole …

Triazolothiadiazoles and Triazolothiadiazines as New and Potent Urease Inhibitors: Insights from In Vitro Assay, Kinetics Data, and In Silico Assessment

J Uddin, S Ullah, SA Halim, M Waqas, A Ibrar… - ACS …, 2023 - ACS Publications
Hyperactivity of the urease enzyme induces the pathogenesis of peptic ulcers and gastritis.
The identification of new urease inhibitors can reduce the activity of urease. Therefore, in the …

Synthesis, analgesic, anti-inflammatory and antimicrobial studies of 2, 4-dichloro-5-fluorophenyl containing thiazolotriazoles

MS Karthikeyan - European journal of medicinal chemistry, 2009 - Elsevier
A series of 2, 4-dichloro-5-fluorophenyl containing thiazolotriazoles (1) were synthesized
starting from 3-(2, 4-dichloro-5-fluorophenyl)-4H-1, 2, 4-triazole-3-thiol (5). The newly …

[HTML][HTML] 6-[3-(4-Fluorophenyl)-1H-pyrazol-4-yl]-3-[(2-naphthyloxy) methyl][1, 2, 4] triazolo [3, 4-b][1, 3, 4] thiadiazole as a potent antioxidant and an anticancer agent …

D Sunil, AM Isloor, P Shetty, K Satyamoorthy… - Arabian Journal of …, 2010 - Elsevier
In this paper we have investigated the in vitro antioxidant property of two triazolo-
thiadiazoles, 6-[3-(4-fluorophenyl)-1H-pyrazol-4-yl]-3-[(2-naphthyloxy) methyl][1, 2, 4] …

Exploration of a library of triazolothiadiazole and triazolothiadiazine compounds as a highly potent and selective family of cholinesterase and monoamine oxidase …

I Khan, SM Bakht, A Ibrar, S Abbas, S Hameed… - RSC Advances, 2015 - pubs.rsc.org
There is a high demand for the collection of small organic molecules (especially N-
heterocycles) with diversity and complexity in the process of drug discovery. This need for …

[HTML][HTML] Synthesis and pharmacological evaluation of 3-diphenylmethyl-6-substituted-1, 2, 4-triazolo [3, 4-b]-1, 3, 4-thiadiazoles: A condensed bridgehead nitrogen …

MW Akhter, MZ Hassan, M Amir - Arabian Journal of Chemistry, 2014 - Elsevier
Abstract A series of 3-diphenylmethyl-6-substituted-1, 2, 4-triazolo [3, 4-b]-1, 3, 4-thiadiazole
derivatives (4a–j and 5a–d) were synthesized by condensation of 4-amino-5-diphenylmethyl …

An overview on 1, 2, 4-triazole and 1, 3, 4-thiadiazole derivatives as potential anesthesic and anti-inflammatory agents

A Koval, A Lozynskyi, R Lesyk - ScienceRise: Pharmaceutical …, 2022 - journals.uran.ua
The aim. The purpose of this review is to summarize data on the synthesis and structural
modification of heterocyclic systems with triazole and thiadiazole fragments in molecules as …

SAR studies on 1, 2, 4-triazolo [3, 4-b][1, 3, 4] thiadiazoles as inhibitors of Mtb shikimate dehydrogenase for the development of novel antitubercular agents

Z Li, Y Liu, X Bai, Q Deng, J Wang, G Zhang, C Xiao… - RSC …, 2015 - pubs.rsc.org
Shikimate dehydrogenase, an essential protein for the biosynthesis of the chorismate end
product, is a highly promising therapeutic target, especially for the discovery and …