Table 1
AOX inhibitors or inhibitor classes
CompoundPubChem CIDStructureReferences
Benzoic acid derivatives 135  [123,234–236] 
Ascofuranone derivatives 6434242  [69,122,125,127,237] 
Decyl-Aurachin C 6439171  [238] 
Chloroquine 2719  [239] 
Coumarin derivatives 5650046  [240] 
Disulfiram 3117  [241] 
Ferulenol 54679300  [126] 
Gallic acid derivatives 61253  [11,235,238,242] 
Hydroxamic acid derivatives 66644  [235,242,243] 
Linoleic acid 5280450  [244–246] 
N-phenylbenzamide derivatives 3532749  [98,247] 
5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole 3016416  [244,248] 
CompoundPubChem CIDStructureReferences
Benzoic acid derivatives 135  [123,234–236] 
Ascofuranone derivatives 6434242  [69,122,125,127,237] 
Decyl-Aurachin C 6439171  [238] 
Chloroquine 2719  [239] 
Coumarin derivatives 5650046  [240] 
Disulfiram 3117  [241] 
Ferulenol 54679300  [126] 
Gallic acid derivatives 61253  [11,235,238,242] 
Hydroxamic acid derivatives 66644  [235,242,243] 
Linoleic acid 5280450  [244–246] 
N-phenylbenzamide derivatives 3532749  [98,247] 
5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole 3016416  [244,248] 

Structures column depicts core inhibitor structures, with R groups indicating positions of functional group manipulation used within the reference list.

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