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01. Food Nutrient & Dietary Chemicals (group results)
Carbohydrate components (1)
Phenolic components [ChEBI:15882] (2)

02. Food Pesticide Chemicals with Regulated Residues on Food Commodities

03. Biological Effects of Specific Chemicals: all > antimicrobial agent [CHEBI:33281] (group results)
antibacterial agent [CHEBI:33282] (4)
antibiotic [CHEBI:22582] (1)
antifungal agent [CHEBI:35718] (5)
antimicrobial drug [CHEBI:36043] (2)
antiviral agent [CHEBI:22587] (2)
disinfectant [CHEBI:48219] (2)
fungicide [CHEBI:24127] (3)

04. Bioactive Capabilities of Specific Chemicals : all > Oxidoreductases [EC:1]
Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] (10)
Acting on the aldehyde or oxo group of donors [EC:1.2] (1)
Acting on the CH-CH group of donors [EC:1.3] (2)
Acting on the CH-NH group of donors [EC:1.5] (1)
Acting on the CH-OH group of donors [EC:1.1] (5)
Reducing C-O-C group as acceptor [EC:1.23] (1)

05. Industrial Uses (group results)
agrochemical [CHEBI:33286] (1)
food additive [CHEBI:64047] (1)
pesticide [CHEBI:25944] (1)
 pharmaceutical [CHEBI:52217] (6)
solvent [CHEBI:46787] (1)

06. Name of Biological Source of Chemical (group results)
Plantae (2)

07. Part of Biological Source of Chemical (group results)
plant structure [PO:0009011] (1)
unspecified structure [PO:0000004] (1)

08. Chemical Category: all > main group molecular entity [CHEBI:33579] > p-block molecular entity [CHEBI:33675] (group results)
carbon group molecular entity [CHEBI:33582] (17)
chalcogen molecular entity [CHEBI:33304] (12)
pnictogen molecular entity [CHEBI:33302] (4)

09. Chemical Capabilities

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04. Bioactive Capabilities of Specific Chemicals : Oxidoreductases [EC:1]
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08. Chemical Category: main group molecular entity [CHEBI:33579] > p-block molecular entity [CHEBI:33675]
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03. Biological Effects of Specific Chemicals: antimicrobial agent [CHEBI:33281]
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17 items, grouped by 04. Bioactive Capabilities of Specific Chemicals  (view ungrouped items)

Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] (10)   
[CHEBI:3900]
 costunolide 
  
  
  
 [CHEBI:8602]
 pseudobaptigenin 
  
  
  
 [CHEBI:15882]
 phenol 
  
  
  
[CHEBI:17097]
 biphenyl 
  
  
  
 [CHEBI:17209]
 dihydrosanguinarine 
  
  
  
 [CHEBI:32023]
 plaunotol 
  
  
  
[CHEBI:52086]
 glyceollin III 
  
  
  
 [CHEBI:62247]
 (1R,2S)-epoxypropylphosphonate(1-) 
  
  
  
 [CHEBI:67153]
 (+)-larreatricin 
  
  
  
[CHEBI:137041]
 quinine(1+) 
  
  
  

Acting on the aldehyde or oxo group of donors [EC:1.2] (1)   
[CHEBI:16731]
 cinnamaldehyde 
  
  
  

Acting on the CH-CH group of donors [EC:1.3] (2)   
[CHEBI:16786]
 vestitone 
  
  
  
 [CHEBI:48981]
 quinolin-8-ol 
  
  
  

Acting on the CH-NH group of donors [EC:1.5] (1)   
[CHEBI:17209]
 dihydrosanguinarine 
  
  
  

Acting on the CH-OH group of donors [EC:1.1] (5)   
[CHEBI:16016]
 glycerone 
  
  
  
 [CHEBI:16236]
 ethanol 
  
  
  
 [CHEBI:16605]
 allyl alcohol 
  
  
  
[CHEBI:16731]
 cinnamaldehyde 
  
  
  
 [CHEBI:16786]
 vestitone 
  
  
  

Reducing C-O-C group as acceptor [EC:1.23] (1)   
[CHEBI:67246]
 (+)-lariciresinol