Discovery of novel thiosemicarbazone derivatives with potent and selective anti-Candida glabrata activity

A series of 21 novel compounds containing a thiosemicarbazone moiety were designed and synthesised based on hit compound 1 from our in-house compound library screening. Most compounds showed potent antifungal activity in vitro against seven common pathogenic fungi. Notably, all compounds showed high...

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Veröffentlicht in:Journal of enzyme inhibition and medicinal chemistry 2023-12, Vol.38 (1), p.2202362-2202362
Hauptverfasser: Li, Xianru, Li, Liping, Zhang, Haonan, Chi, Xiaochen, Jiang, Yuanying, Ni, Tingjunhong
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container_title Journal of enzyme inhibition and medicinal chemistry
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creator Li, Xianru
Li, Liping
Zhang, Haonan
Chi, Xiaochen
Jiang, Yuanying
Ni, Tingjunhong
description A series of 21 novel compounds containing a thiosemicarbazone moiety were designed and synthesised based on hit compound 1 from our in-house compound library screening. Most compounds showed potent antifungal activity in vitro against seven common pathogenic fungi. Notably, all compounds showed high potency against Candida glabrata 537 (MIC = ≤0.0156-2 µg/mL). Of note, compounds 5j and 5r displayed excellent antifungal activity against Candida krusei 4946 and Candida auris 922. Additionally, compounds 5j and 5r also showed high potency against 15 C. glabrata isolates with MIC values ranging from 0.0625 µg/mL to 4 µg/mL, with compound 5r being slightly superior to 5j. Moreover, compound 5r has certain effect against biofilm formation of C. glabrata. Furthermore, compound 5r has minimal cytotoxicity against HUVECs with an IC 50 value of 15.89 µg/mL and no haemolysis at 64 µg/mL. Taken together, these results suggest that promising lead compound 5r deserves further investigation.
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Most compounds showed potent antifungal activity in vitro against seven common pathogenic fungi. Notably, all compounds showed high potency against Candida glabrata 537 (MIC = ≤0.0156-2 µg/mL). Of note, compounds 5j and 5r displayed excellent antifungal activity against Candida krusei 4946 and Candida auris 922. Additionally, compounds 5j and 5r also showed high potency against 15 C. glabrata isolates with MIC values ranging from 0.0625 µg/mL to 4 µg/mL, with compound 5r being slightly superior to 5j. Moreover, compound 5r has certain effect against biofilm formation of C. glabrata. Furthermore, compound 5r has minimal cytotoxicity against HUVECs with an IC 50 value of 15.89 µg/mL and no haemolysis at 64 µg/mL. 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subjects antifungal
Antifungal activity
Antifungal agents
Antifungal Agents - pharmacology
Candida glabrata
Cytotoxicity
Drug resistance
Fungal infections
Fungi
Hospitals
Hydroxy-phenylhydrazone
Medicine
Microbial Sensitivity Tests
Minimum inhibitory concentration
Pathogens
Pharmacy
Research Paper
structure-activity relationship
synthesis
thiosemicarbazone
title Discovery of novel thiosemicarbazone derivatives with potent and selective anti-Candida glabrata activity
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