[HTML][HTML] Grandisin and its therapeutic potential and pharmacological activities: A review

DK Patel - Pharmacological Research-Modern Chinese Medicine, 2022 - Elsevier
Plant derived products and phytoconstituents have been used in medicine for the treatment
of human disorders and associated secondary complication since a very early age …

Insights into the current status of privileged N-heterocycles as antileishmanial agents

N Razzaghi-Asl, S Sepehri, A Ebadi, P Karami… - Molecular …, 2020 - Springer
Leishmania, one of the most important neglected tropical diseases, is endemic in several
regions of the world and hence regarded as a serious threat to public health. Major …

A step-by-step synthesis of triazole-benzimidazole-chalcone hybrids: Anticancer activity in human cells+

A Djemoui, A Naouri, MR Ouahrani, D Djemoui… - Journal of Molecular …, 2020 - Elsevier
Novel series of triazole-benzimidazole-chalcone hybrid compounds have been synthesized
via click chemistry, between different azide derivatives and substituted benzimidazole …

Design, synthesis, antileishmanial, and antifungal biological evaluation of novel 3, 5‐disubstituted isoxazole compounds based on 5‐nitrofuran scaffolds

OS Trefzger, NV Barbosa… - Archiv der …, 2020 - Wiley Online Library
Abstract Nineteen 3, 5‐disubstituted‐isoxazole analogs were synthesized based on
nitrofuran scaffolds, by a [3+ 2] cycloaddition reaction between terminal acetylenes and 5 …

Design, synthesis and antitrypanosomatid activity of 2-nitroimidazole-3, 5-disubstituted isoxazole compounds based on benznidazole

DB Carvalho, PAN Costa, GB Portapilla… - European Journal of …, 2023 - Elsevier
Chagas disease and leishmaniasis are neglected diseases of high priority as a public health
problem. Pharmacotherapy is based on the administration of a few drugs, which exhibit …

Design and Synthesis of Novel 3-Nitro-1H-1,2,4-triazole-1,2,3-triazole-1,4-disubstituted Analogs as Promising Antitrypanosomatid Agents: Evaluation of In Vitro …

BI Pelizaro, JCZ Batista, GB Portapilla… - Journal of Medicinal …, 2024 - ACS Publications
A series of 28 compounds, 3-nitro-1 H-1, 2, 4-triazole, were synthesized by click-chemistry
with diverse substitution patterns using medicinal chemistry approaches, such as …

Anti-inflammatory, ulcerogenic and platelet activation evaluation of novel 1, 4-diaryl-1, 2, 3-triazole neolignan-celecoxib hybrids

JL Felipe, TB Cassamale, LD Lourenco… - Bioorganic …, 2022 - Elsevier
This study reports the synthesis of novel neolignans-celecoxib hybrids and the evaluation of
their biological activity. Analogs 8–13 (L13-L18) exhibited anti-inflammatory activity …

Design, synthesis and biological evaluation of novel 1, 2, 3-triazole-based xanthine derivatives as DPP-4 inhibitors

S Narsimha, KS Battula, M Ravinder, YN Reddy… - Journal of Chemical …, 2020 - Springer
Inhibitors of dipeptidyl peptidase-4 (DPP4) have been shown to be effective treatments for
type 2 diabetes. A series of novel 1, 2, 3-triazole based xanthine derivatives were designed …

Phytochemical constituents from Scutellaria baicalensis in soluble epoxide hydrolase inhibition: Kinetics and interaction mechanism merged with simulations

ZB Liu, CP Sun, JX Xu, C Morisseau… - International journal of …, 2019 - Elsevier
In our search for soluble epoxide hydrolase (sEH) inhibitors from plants, we found that water
extracts of Scutellaria baicalensis Georgi displayed significant inhibitory activity against sEH …

Design, synthesis and antitrypanosomatid activities of 3, 5‐diaryl‐isoxazole analogues based on neolignans veraguensin, grandisin and machilin G

OS Trefzger, AR das Neves, NV Barbosa… - Chemical Biology & …, 2019 - Wiley Online Library
Using bioisosterism as a medicinal chemistry tool, 16 3, 5‐diaryl‐isoxazole analogues of the
tetrahydrofuran neolignans veraguensin, grandisin and machilin G were synthesized via 1, 3 …