新生隐球菌
唑
生物膜
一氧化氮
化学
抗真菌
隐球菌病
鼻腔给药
隐球菌
微生物学
药品
隐球菌性脑膜炎
药理学
效力
体外
医学
细菌
人类免疫缺陷病毒(HIV)
生物化学
免疫学
生物
遗传学
有机化学
病毒性疾病
作者
Fangfang Wang,Jianbing Wu,Mingke Yuan,Zhengsheng Yan,Xin Liu,Wang Li,Yihua Zhang,Chunquan Sheng,Na Liu,Zhangjian Huang
标识
DOI:10.1021/acs.jmedchem.3c01308
摘要
Invasive fungal infections (IFIs) such as cryptococcal meningitis (CM) remain a serious health issue worldwide due to drug resistance closely related to biofilm formation. Unfortunately, available antifungal drugs with ideal safety and promising potency are still lacking; thus, the research of new candidate and therapeutic approach is urgently needed. As an important gas messenger molecule, nitric oxide (NO) shows vital inhibition on various microorganism biofilms. Hence, three series of novel NO-donating azole derivatives were designed and synthesized, and the in vitro antifungal activity as well as the mechanism of action was investigated. Among them, 3a and 3e displayed excellent antifungal activity against Cryptococcus neoformans and biofilm depending on the release of NO. Moreover, a more stable analogue 3h of 3a demonstrated markedly anti-CM effects via intranasal dropping, avoiding the first-pass effects and possessing a better brain permeability bypass blood-brain barrier. These results present a promising antifungal candidate and intranasal dropping approach for the treatment of CM, warranting further studies.
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