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N-Aryl-3,4-dihydroisoquinoline Carbothioamide Analogues as Potential Urease Inhibitors
[Image: see text] N-Aryl-3,4-dihydroisoquinoline carbothioamide analogues 1–22 were synthesized by a simple one-step reaction protocol and subjected to in vitro urease inhibition studies for the first time. All compounds 1–22 were found active and showed significant to moderate urease inhibitory pot...
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| Publié dans: | ACS Omega |
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| Auteurs principaux: | , , , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
American Chemical Society
2021
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| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8223216/ https://ncbi.nlm.nih.gov/pubmed/34179623 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acsomega.1c01182 |
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