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01. Food Nutrient & Dietary Chemicals (group results)
Lipid components [ChEBI:18059] (1)
Nitrogen components (2)
Phenolic components [ChEBI:15882] (6)
Vitamins [ChEBI:26848] (4)

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] (6)
enzyme inhibitor [CHEBI:23924] (5)
metabolite [CHEBI:25212] (70)
photobiochemical uses [CHEBI:52216] (4)

04. Bioactive Capabilities of Specific Chemicals : all > Oxidoreductases [EC:1]
Acting on CH or CH2 groups [EC:1.17] (8)
Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] (39)
Acting on single donors with incorporation of molecular oxygen (oxygenases) [EC:1.13] (4)
Acting on the aldehyde or oxo group of donors [EC:1.2] (7)
Acting on the CH-CH group of donors [EC:1.3] (10)
Acting on the CH-NH group of donors [EC:1.5] (8)
Acting on the CH-NH2 group of donors [EC:1.4] (3)
Acting on the CH-OH group of donors [EC:1.1] (22)
Acting on X-H and Y-H to form an X-Y bond [EC:1.21] (4)
Reducing C-O-C group as acceptor [EC:1.23] (4)

05. Industrial Uses (group results)
anti-inflammatory agent [CHEBI:67079] (1)
food additive [CHEBI:64047] (3)
fragrance [CHEBI:48318] (1)
pesticide [CHEBI:25944] (1)
pharmaceutical [CHEBI:52217] (16)
solvent [CHEBI:46787] (1)

06. Name of Biological Source of Chemical (group results)
Fungi, Yeasts, Molds and Mildews (2)
 Plantae (15)

07. Part of Biological Source of Chemical (group results)
fungal structure [FS:0000000] (1)
plant structure [PO:0009011] (11)
unspecified structure [PO:0000004] (8)

08. Chemical Category: all > polyatomic entity [CHEBI:36357] > molecule [CHEBI:25367] (group results)
cyclic compound [CHEBI:33595] (68)
 organic molecule [CHEBI:72695] (81)

09. Chemical Capabilities (group results)
antioxidant [CHEBI:22586] (4)

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04. Bioactive Capabilities of Specific Chemicals : Oxidoreductases [EC:1]
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08. Chemical Category: polyatomic entity [CHEBI:36357] > molecule [CHEBI:25367]
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03. Biological Effects of Specific Chemicals: biochemical uses [CHEBI:52206]
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81 items, grouped by 04. Bioactive Capabilities of Specific Chemicals  (view ungrouped items)

Acting on CH or CH2 groups [EC:1.17] (8)   
[CHEBI:15600]
 (+)-catechin 
  
  
  
 [CHEBI:17368]
 hypoxanthine 
  
  
  
 [CHEBI:17568]
 uracil 
  
  
  
[CHEBI:17597]
 4-hydroxybenzaldehyde 
  
  
  
all 8 items...

Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] (39)   
[CHEBI:3900]
 costunolide 
  
  
  
 [CHEBI:8602]
 pseudobaptigenin 
  
  
  
 [CHEBI:9192]
 solavetivone 
  
  
  
[CHEBI:15347]
 acetone 
  
  
  
all 39 items...

Acting on single donors with incorporation of molecular oxygen (oxygenases) [EC:1.13] (4)   
[CHEBI:2311]
 Oplophorus luciferin 
  
  
  
 [CHEBI:16531]
 Renilla luciferin 
  
  
  
 [CHEBI:17959]
 oxidized Renilla luciferin 
  
  
  
[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 
  
  
  
all 7 items...

Acting on the CH-CH group of donors [EC:1.3] (10)   
[CHEBI:15901]
 5,6-dihydrouracil 
  
  
  
 [CHEBI:16118]
 berberine 
  
  
  
 [CHEBI:16592]
 (S)-canadine 
  
  
  
[CHEBI:16786]
 vestitone 
  
  
  
all 10 items...

Acting on the CH-NH group of donors [EC:1.5] (8)   
[CHEBI:15372]
 5,6,7,8-tetrahydrobiopterin 
  
  
  
 [CHEBI:15373]
 biopterin 
  
  
  
 [CHEBI:16118]
 berberine 
  
  
  
[CHEBI:16708]
 adenine 
  
  
  
all 8 items...

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] (22)   
[CHEBI:4372]
 (6S)-dehydrovomifoliol 
  
  
  
 [CHEBI:15347]
 acetone 
  
  
  
 [CHEBI:15421]
 perillyl aldehyde 
  
  
  
[CHEBI:16335]
 adenosine 
  
  
  
all 22 items...

Acting on X-H and Y-H to form an X-Y bond [EC:1.21] (4)   
[CHEBI:16118]
 berberine 
  
  
  
 [CHEBI:16159]
 sulochrin 
  
  
  
 [CHEBI:17129]
 (S)-scoulerine 
  
  
  
[CHEBI:17750]
 glycine betaine 
  
  
  

Reducing C-O-C group as acceptor [EC:1.23] (4)   
[CHEBI:40]
 (+)-pinoresinol 
  
  
  
 [CHEBI:65004]
 (-)-secoisolariciresinol 
  
  
  
 [CHEBI:67245]
 (-)-pinoresinol 
  
  
  
[CHEBI:67246]
 (+)-lariciresinol