[HTML][HTML] Synthesis and biological activity of novel 4-aminoquinoline/1, 2, 3-triazole hybrids against Leishmania amazonensis

N Glanzmann, LMR Antinarelli… - Biomedicine & …, 2021 - Elsevier
Abstract Quinoline and 1, 2, 3-triazoles are well-known nitrogen-based heterocycles
presenting diverse pharmacological properties, although their antileishmanial activity is still …

Synthesis of 1,2,3-Triazole-Containing Methoxylated Cinnamides and Their Antileishmanial Activity against the Leishmania braziliensis Species

FS Santos, RP Freitas, CS Freitas, DVC Mendonça… - Pharmaceuticals, 2023 - mdpi.com
Leishmaniasis is a group of infectious diseases caused by protozoan parasites that belong
to the genus Leishmania. Currently, there is no human vaccine, and the available treatments …

Synthesis and antileishmanial evaluation of 1-aryl-4-(4, 5-dihydro-1H-imidazol-2-yl)-1H-pyrazole derivatives

MS dos Santos, MLV Oliveira, AMR Bernardino… - Bioorganic & medicinal …, 2011 - Elsevier
A series of 1-aryl-4-(4, 5-dihydro-1H-imidazol-2-yl)-1H-pyrazoles (4a–g) and 5-amino-1-aryl-
4-(4, 5-dihydro-1H-imidazol-2-yl)-1H-pyrazoles (5a–g) were synthesized and evaluated in …

1,4-Disubstituted-1,2,3-Triazole Compounds Induce Ultrastructural Alterations in Leishmania amazonensis Promastigote: An in Vitro Antileishmanial and in Silico …

F Almeida-Souza, VD Silva, GX Silva… - International Journal of …, 2020 - mdpi.com
The current standard treatment for leishmaniasis has remained the same for over 100 years,
despite inducing several adverse effects and increasing cases of resistance. In this study we …

Antileishmanial activity and structure-activity relationship of triazolic compounds derived from the neolignans grandisin, veraguensin, and machilin G

EC Costa, TB Cassamale, DB Carvalho… - Molecules, 2016 - mdpi.com
Sixteen 1, 4-diaryl-1, 2, 3-triazole compounds 4–19 derived from the tetrahydrofuran
neolignans veraguensin 1, grandisin 2, and machilin G 3 were tested against Leishmania …

Design and synthesis of novel tetrahydronaphthyl azoles and related cyclohexyl azoles as antileishmanial agents

VK Marrapu, N Srinivas, M Mittal, N Shakya… - Bioorganic & medicinal …, 2011 - Elsevier
A novel series of trans-2-aryloxy-1, 2, 3, 4,-tetrahydronaphthyl azoles and related cyclohexyl
azoles were synthesized and evaluated in vitro against Leishmania donovani. Compound 9 …

Synthesis and evaluation of novel triazolyl quinoline derivatives as potential antileishmanial agents

A Upadhyay, P Kushwaha, S Gupta, RP Dodda… - European Journal of …, 2018 - Elsevier
The high potential of quinoline containing natural products and their derivatives in medicinal
chemistry led us to discover novel series of 25 compounds for the development of new …

Effectiveness of Novel 5‐(5‐amino‐1‐aryl‐1H‐pyrazol‐4‐yl)‐1H‐tetrazole Derivatives Against Promastigotes and Amastigotes of Leishmania amazonensis

V dos Santos Faiões, LL Leon… - Chemical Biology & …, 2014 - Wiley Online Library
In this research, a series of substituted 5‐(5‐amino‐1‐aryl‐1H‐pyrazol‐4‐yl)‐1H‐tetrazoles
were synthesized and evaluated for in vitro antileishmanial activity. Among the derivatives …

Synthesis, biological evaluation, structure–activity relationship, and mechanism of action studies of quinoline–metronidazole derivatives against experimental visceral …

A Upadhyay, P Chandrakar, S Gupta… - Journal of Medicinal …, 2019 - ACS Publications
In our efforts to identify novel chemical scaffolds for the development of antileishmanial
agents, a series of quinoline–metronidazole hybrid compounds was synthesized and tested …

Synthesis and biological evaluation against Leishmania donovani of novel hybrid molecules containing indazole-based 2-pyrone scaffolds

M El Ghozlani, L Bouissane, M Berkani, S Mojahidi… - …, 2019 - pubs.rsc.org
A series of novel indazole–pyrone hybrids were synthesized by a one pot reaction between
N-alkyl-6 (5)-nitroindazoles and 2-pyrone (4-hydroxy-6-methyl-2H-pyran-2-one) using …