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Published in 2022 at "Chemmedchem"
DOI: 10.1002/cmdc.202200023
Abstract: Leishmaniasis is a vector‐borne neglected parasitic infection affecting thousands of individuals, mostly among populations in low‐ to moderate‐income developing countries. In the absence of protective vaccines, the management of the disease banks solely on chemotherapy.…
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Keywords:
nitrofurantoin triazole;
synthesis vitro;
efficacy hit;
vitro antileishmanial ... See more keywords
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1
Published in 2018 at "Journal of Heterocyclic Chemistry"
DOI: 10.1002/jhet.3010
Abstract: A new set of ciprofloxacin (CPFX)-isatin-1H-1,2,3-triazole hybrids 6a–l with greater lipophilicity compared with the parent CPFX was designed, synthesized, and assessed for their in vitro anti-mycobacterial activity against Mycobacterium tuberculosis (MTB) H37Rv as well as…
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Keywords:
isatin triazole;
triazole hybrids;
vitro anti;
ciprofloxacin ... See more keywords
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Published in 2020 at "Medicinal Chemistry Research"
DOI: 10.1007/s00044-020-02553-0
Abstract: Infectious diseases such as tuberculosis and leishmaniasis are leading causes of human death. One of the major factors contributing to the poor control of these diseases is primarily the reduced effectiveness of the existing chemotherapies…
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Keywords:
vitro antimycobacterial;
triazole hybrids;
hydroquinone triazole;
chemistry ... See more keywords
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Published in 2019 at "Bioorganic chemistry"
DOI: 10.1016/j.bioorg.2019.102967
Abstract: A series of 12 novel 1,4-naphthoquinone-1,2,3-triazole hybrids were designed and synthesized through copper-catalyzed click reaction of 2-(prop-2-ynylamino)naphthalene-1,4-dione (3) and different azidomethyl-benzene derivatives. The synthesized compounds were assessed for their anticancer activity against three cancer cell…
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Keywords:
triazole hybrids;
chemistry;
cell cycle;
cancer cell ... See more keywords
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Published in 2019 at "Journal of Molecular Structure"
DOI: 10.1016/j.molstruc.2019.04.082
Abstract: Abstract A new series of thiosemicarbazide-1,2,3-triazole hybrids 10a-o has been synthesized, characterized by 1H NMR, 13C NMR, and screened for their in vitro α-glucosidase inhibitory activity. All of the synthesized compounds displayed excellent α-glucosidase inhibitory activity…
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Keywords:
hybrids potent;
new thiosemicarbazide;
potent glucosidase;
compound 10h ... See more keywords
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2
Published in 2022 at "ACS Omega"
DOI: 10.1021/acsomega.2c06531
Abstract: Cancer is the most severe disease worldwide. Every year, tens of millions of people are diagnosed with cancer, and over half of those people will ultimately die from the disease. Hence, the discovery of new…
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Keywords:
liver cancer;
cancer cells;
indolyl triazole;
triazole hybrids ... See more keywords
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2
Published in 2023 at "ACS Omega"
DOI: 10.1021/acsomega.2c07993
Abstract: Coumarin is a naturally occurring bioactive pharmacophore with wide occurrence among central nervous system (CNS)-active small molecules. 8-Acetylcoumarin, one of the natural coumarins, is a mild inhibitor of cholinesterases and β-secretase, which are vital targets…
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Keywords:
synthesis biological;
biological evaluation;
coumarin;
triazole hybrids ... See more keywords
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Published in 2022 at "International Journal of Molecular Sciences"
DOI: 10.3390/ijms232214291
Abstract: Resistance to antibiotics is an emerging problem worldwide, which leads to an increase in morbidity and mortality rates. Several mechanisms are attributed to bacterial resistance, overexpression of efflux pumps being one of the most prominent.…
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Keywords:
chalcone triazole;
activity;
resistance;
new chalcone ... See more keywords
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2
Published in 2023 at "Molecules"
DOI: 10.3390/molecules28020626
Abstract: Hybrid compounds of flavones, namely chrysin and kaempferol, and substituted 1,2,3-triazole derivatives, were synthesized by click reaction of the intermediate O-propargyl derivatives. 4-Fluoro- and 4-nitrobenzyl-1,2,3-triazole-containing hybrid molecules were prepared. The mono- and bis-coupled hybrids were…
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Keywords:
vitro anticancer;
synthesis vitro;
flavone triazole;
triazole hybrids ... See more keywords
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Published in 2023 at "Future medicinal chemistry"
DOI: 10.4155/fmc-2022-0289
Abstract: Aim: α-Glucosidase inhibitors are important oral antidiabetic drugs that are used alone or in combination therapy. Materials & methods: In this regard, 1,3,4-thiadiazoles-1,2,3-triazoles were designed, synthesized and evaluated for α-glucosidase enzyme inhibition. Results: The applied…
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Keywords:
inhibition;
glucosidase;
click inspired;
thiadiazole triazole ... See more keywords