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01. Food Nutrient & Dietary Chemicals (group results)
Phenolic components [ChEBI:15882] (2)
Vitamins [ChEBI:26848] (2)

02. Food Pesticide Chemicals with Regulated Residues on Food Commodities

03. Biological Effects of Specific Chemicals: all > biochemical uses [CHEBI:52206] (group results)
cofactor [CHEBI:23357] (2)
enzyme inhibitor [CHEBI:23924] (3)
metabolite [CHEBI:25212] (24)
photobiochemical uses [CHEBI:52216] (1)

04. Bioactive Capabilities of Specific Chemicals : all > Oxidoreductases [EC:1]
Acting on CH or CH2 groups [EC:1.17] (1)
Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] (13)
Acting on single donors with incorporation of molecular oxygen (oxygenases) [EC:1.13] (1)
Acting on the aldehyde or oxo group of donors [EC:1.2] (7)
Acting on the CH-CH group of donors [EC:1.3] (1)
Acting on the CH-NH group of donors [EC:1.5] (1)
Acting on the CH-NH2 group of donors [EC:1.4] (3)
Acting on the CH-OH group of donors [EC:1.1] (14)
Acting on X-H and Y-H to form an X-Y bond [EC:1.21] (2)

05. Industrial Uses (group results)
anti-inflammatory agent [CHEBI:67079] (1)
food additive [CHEBI:64047] (3)
fragrance [CHEBI:48318] (1)
pharmaceutical [CHEBI:52217] (4)
solvent [CHEBI:46787] (1)

06. Name of Biological Source of Chemical (group results)
Plantae (5)

07. Part of Biological Source of Chemical (group results)
plant structure [PO:0009011] (3)
unspecified structure [PO:0000004] (3)

08. Chemical Category: all > main group molecular entity [CHEBI:33579] > p-block molecular entity [CHEBI:33675] > chalcogen molecular entity [CHEBI:33304] > oxygen molecular entity [CHEBI:25806] > organooxygen compound [CHEBI:36963] > carbonyl compound [CHEBI:36586] (group results)
aldehyde [CHEBI:17478] (8)
carboxylic acid [CHEBI:33575] (3)
carboxylic ester [CHEBI:33308] (6)
 ketone body [CHEBI:73693] (1)
ketone [CHEBI:17087] (14)

09. Chemical Capabilities (group results)
antioxidant [CHEBI:22586] (2)

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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] > chalcogen molecular entity [CHEBI:33304] > oxygen molecular entity [CHEBI:25806] > organooxygen compound [CHEBI:36963] > carbonyl compound [CHEBI:36586]
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03. Biological Effects of Specific Chemicals: biochemical uses [CHEBI:52206]
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30 items, grouped by 04. Bioactive Capabilities of Specific Chemicals  (view ungrouped items)

Acting on CH or CH2 groups [EC:1.17] (1)   
[CHEBI:17597]
 4-hydroxybenzaldehyde 
  
  
  

Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] (13)   
[CHEBI:3900]
 costunolide 
  
  
  
 [CHEBI:8602]
 pseudobaptigenin 
  
  
  
 [CHEBI:9192]
 solavetivone 
  
  
  
[CHEBI:15347]
 acetone 
  
  
  
 [CHEBI:16794]
 scopolamine 
  
  
  
 [CHEBI:17281]
 2-deoxy-D-ribono-1,4-lactone 
  
  
  
[CHEBI:17793]
 calycosin 
  
  
  
 [CHEBI:18015]
 oxidized Latia luciferin 
  
  
  
 [CHEBI:18067]
 phylloquinone 
  
  
  
[CHEBI:28032]
 4'-hydroxyacetophenone 
  
  
  
 [CHEBI:28777]
 liquiritigenin 
  
  
  
 [CHEBI:63664]
 taxusin 
  
  
  
[CHEBI:63665]
 7beta-hydroxytaxusin 
  
  
  

Acting on single donors with incorporation of molecular oxygen (oxygenases) [EC:1.13] (1)   
[CHEBI:18346]
 vanillin 
  
  
  

Acting on the aldehyde or oxo group of donors [EC:1.2] (7)   
[CHEBI:16424]
 phenylacetaldehyde 
  
  
  
 [CHEBI:16731]
 cinnamaldehyde 
  
  
  
 [CHEBI:17169]
 benzaldehyde 
  
  
  
[CHEBI:17310]
 pyridoxal 
  
  
  
 [CHEBI:17597]
 4-hydroxybenzaldehyde 
  
  
  
 [CHEBI:17750]
 glycine betaine 
  
  
  
[CHEBI:18346]
 vanillin 
  
  
  

Acting on the CH-CH group of donors [EC:1.3] (1)   
[CHEBI:16786]
 vestitone 
  
  
  

Acting on the CH-NH group of donors [EC:1.5] (1)   
[CHEBI:29985]
 L-glutamate(1-) 
  
  
  

Acting on the CH-NH2 group of donors [EC:1.4] (3)   
[CHEBI:16424]
 phenylacetaldehyde 
  
  
  
 [CHEBI:29985]
 L-glutamate(1-) 
  
  
  
 [CHEBI:58359]
 L-glutamine zwitterion 
  
  
  

Acting on the CH-OH group of donors [EC:1.1] (14)   
[CHEBI:4372]
 (6S)-dehydrovomifoliol 
  
  
  
 [CHEBI:15347]
 acetone 
  
  
  
 [CHEBI:15421]
 perillyl aldehyde 
  
  
  
[CHEBI:16731]
 cinnamaldehyde 
  
  
  
 [CHEBI:16786]
 vestitone 
  
  
  
 [CHEBI:17310]
 pyridoxal 
  
  
  
[CHEBI:17597]
 4-hydroxybenzaldehyde 
  
  
  
 [CHEBI:17750]
 glycine betaine 
  
  
  
 [CHEBI:17889]
 isopyridoxal 
  
  
  
[CHEBI:18067]
 phylloquinone 
  
  
  
 [CHEBI:18346]
 vanillin 
  
  
  
 [CHEBI:63892]
 zerumbone 
  
  
  
[CHEBI:63906]
 cholest-5-en-3-one 
  
  
  
 [CHEBI:71634]
 hydroxyversicolorone 
  
  
  

Acting on X-H and Y-H to form an X-Y bond [EC:1.21] (2)   
[CHEBI:16159]
 sulochrin 
  
  
  
 [CHEBI:17750]
 glycine betaine