Anti-tuberculosis activity and its structure-activity relationship (SAR) studies of oxadiazole derivatives: A key review

SK Verma, R Verma, S Verma, Y Vaishnav… - European Journal of …, 2021 - Elsevier
With the increasing number of cases of inactive and drug-resistance tuberculosis, there is an
urgent need to develop new potent molecules set for fighting this brutal disease. Medicinal …

Recent advancements and developments in search of anti-tuberculosis agents: a quinquennial update and future directions

TM Dhameliya, KA Bhakhar, ND Gajjar, KA Patel… - Journal of Molecular …, 2022 - Elsevier
Tuberculosis (TB) has been considered as the highly chronic, contagious and infectious
disorder caused by Mycobacterium tuberculosis (Mtb). Every year more than 10 million …

Ferulic, sinapic, 3, 4-dimethoxycinnamic acid and indomethacin derivatives with antioxidant, anti-inflammatory and hypolipidemic functionality

P Theodosis-Nobelos, G Papagiouvannis, EA Rekka - Antioxidants, 2023 - mdpi.com
A series of thiomorpholine and cinnamyl alcohol derivatives, conjugated with cinnamic acid-
containing moieties, such as ferulic acid, sinapic acid and 3, 4-dimethoxycinnamic acid …

Development of sulfonamide-based Schiff bases targeting urease inhibition: Synthesis, characterization, inhibitory activity assessment, molecular docking and ADME …

A Hamad, MA Khan, KM Rahman, I Ahmad… - Bioorganic …, 2020 - Elsevier
A series of Sulfonamide-based Schiff bases (E)-4-(benzylideneamino)-N-(6-
methoxypyridazin-3-yl) benzenesulfonamide (3a-r) targeting Urease Inhibition was …

Synthesis, antioxidant activity, docking simulation, and computational investigation of novel heterocyclic compounds and Schiff bases from picric acid

H Bayrak, AM Fahim, FY Karahalil, I Azafad… - Journal of Molecular …, 2023 - Elsevier
In this elucidation, we used the available picric acid commercial for the synthesis of different
heterocyclics such as carbothioamide and 1, 3, 4-oxadiazole and different Schiff bases …

Recent efforts in the discovery of urease inhibitor identifications

WQ Song, ML Liu, SY Li, ZP Xiao - Current Topics in Medicinal …, 2022 - ingentaconnect.com
Urease is an attractive drug target for designing anti-infective agents against pathogens
such as Helicobacter pylori, Proteus mirabilis, and Ureaplasma urealyticum. In the past …

Synthesis, docking and evaluation of in vitro anti-inflammatory activity of novel morpholine capped β-lactam derivatives

R Heiran, S Sepehri, A Jarrahpour, C Digiorgio… - Bioorganic …, 2020 - Elsevier
This study reports the synthesis and biological investigation of three series of novel
monocyclic β-lactam derivatives bearing a morpholine ring substituent on the nitrogen. The …

Electrochemical oxidative synthesis of 1, 3, 4-thiadiazoles from isothiocyanates and hydrazones

Z Ma, X Hu, Y Li, D Liang, Y Dong, B Wang… - Organic Chemistry …, 2021 - pubs.rsc.org
A 2, 3-dichloro-5, 6-dicyano-1, 4-benzoquinone (DDQ)-catalysed electrochemical synthesis
of 2-amino-1, 3, 4-thiadiazoles from isothiocyanates and hydrazones is presented. This …

[HTML][HTML] Synthesis of hydrazides of heterocyclic amines and their antimicrobial and spasmolytic activity

DA Berillo, MA Dyusebaeva - Saudi Pharmaceutical Journal, 2022 - Elsevier
Un unsolvable issue of a significant number increase of drug multi resistant strains of
microorganisms including Mycobacterium tuberculosis force researchers for continuous …

Design, synthesis, molecular prediction and biological evaluation of pyrazole-azomethine conjugates as antimicrobial agents

SS Mukhtar, AS Hassan, NM Morsy… - Synthetic …, 2021 - Taylor & Francis
A series of Schiff bases linked with heterocyclic moiety (6a–c, 7a–c, 11a–c, 12a–c, and 13a–
c) and ferrocenyl Schiff bases (15a–c) were designed, synthesized, and confirmed based on …