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Inhibition of α-, β-, γ-, δ-, ζ- and η-class carbonic anhydrases from bacteria, fungi, algae, diatoms and protozoans with famotidine

Famotidine, an antiulcer drug belonging to the H(2) antagonists class of pharmacological agents, was recently shown to potently inhibit human (h) and bacterial carbonic anhydrases (CAs, EC 4.2.1.1). We investigated the inhibitory effects of famotidine against all classes of CAs from the pathogenic b...

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書目詳細資料
發表在:J Enzyme Inhib Med Chem
Main Authors: Angeli, Andrea, Pinteala, Mariana, Maier, Stelian S., Del Prete, Sonia, Capasso, Clemente, Simionescu, Bogdan C., Supuran, Claudiu T.
格式: Artigo
語言:Inglês
出版: Taylor & Francis 2019
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6366436/
https://ncbi.nlm.nih.gov/pubmed/30727781
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/14756366.2019.1571273
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