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

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] (5)
enzyme inhibitor [CHEBI:23924] (2)
metabolite [CHEBI:25212] (44)
photobiochemical uses [CHEBI:52216] (3)

04. Bioactive Capabilities of Specific Chemicals : all > Oxidoreductases [EC:1]
Acting on CH or CH2 groups [EC:1.17] (7)
Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] (25)
Acting on single donors with incorporation of molecular oxygen (oxygenases) [EC:1.13] (3)
Acting on the aldehyde or oxo group of donors [EC:1.2] (1)
Acting on the CH-CH group of donors [EC:1.3] (9)
Acting on the CH-NH group of donors [EC:1.5] (7)
Acting on the CH-OH group of donors [EC:1.1] (7)
Acting on X-H and Y-H to form an X-Y bond [EC:1.21] (2)
Reducing C-O-C group as acceptor [EC:1.23] (3)

05. Industrial Uses (group results)
pesticide [CHEBI:25944] (1)
 pharmaceutical [CHEBI:52217] (10)

06. Name of Biological Source of Chemical (group results)
Plantae (12)

07. Part of Biological Source of Chemical (group results)
plant structure [PO:0009011] (8)
unspecified structure [PO:0000004] (6)

08. Chemical Category: all > main group molecular entity [CHEBI:33579] > p-block molecular entity [CHEBI:33675] > carbon group molecular entity [CHEBI:33582] > organic molecular entity [CHEBI:50860] > heteroorganic entity [CHEBI:33285] > organic heterocyclic compound [CHEBI:24532] (group results)
heteroarene [CHEBI:33833] (12)
organic heteromonocyclic compound [CHEBI:25693] (18)
organic heteropolycyclic compound [CHEBI:38166] (33)
organonitrogen heterocyclic compound [CHEBI:38101] (35)
oxacycle [CHEBI:38104] (20)

09. Chemical Capabilities (group results)
antioxidant [CHEBI:22586] (3)

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[CHEBI:28938]
 ammonium 
  
  
  
 
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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] > carbon group molecular entity [CHEBI:33582] > organic molecular entity [CHEBI:50860] > heteroorganic entity [CHEBI:33285] > organic heterocyclic compound [CHEBI:24532]
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03. Biological Effects of Specific Chemicals: biochemical uses [CHEBI:52206]
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50 items, grouped by 04. Bioactive Capabilities of Specific Chemicals  (view ungrouped items)

Acting on CH or CH2 groups [EC:1.17] (7)   
[CHEBI:15600]
 (+)-catechin 
  
  
  
 [CHEBI:17368]
 hypoxanthine 
  
  
  
 [CHEBI:17568]
 uracil 
  
  
  
[CHEBI:17712]
 9H-xanthine 
  
  
  
 [CHEBI:17821]
 thymine 
  
  
  
 [CHEBI:27732]
 caffeine 
  
  
  
[CHEBI:32544]
 nicotinate 
  
  
  

Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] (25)   
[CHEBI:3900]
 costunolide 
  
  
  
 [CHEBI:8602]
 pseudobaptigenin 
  
  
  
 [CHEBI:15372]
 5,6,7,8-tetrahydrobiopterin 
  
  
  
[CHEBI:16415]
 protopine 
  
  
  
 [CHEBI:16592]
 (S)-canadine 
  
  
  
 [CHEBI:16704]
 uridine 
  
  
  
[CHEBI:16794]
 scopolamine 
  
  
  
 [CHEBI:17129]
 (S)-scoulerine 
  
  
  
 [CHEBI:17209]
 dihydrosanguinarine 
  
  
  
[CHEBI:17281]
 2-deoxy-D-ribono-1,4-lactone 
  
  
  
 [CHEBI:17568]
 uracil 
  
  
  
 [CHEBI:17712]
 9H-xanthine 
  
  
  
[CHEBI:17789]
 dihydrochelirubine 
  
  
  
 [CHEBI:17793]
 calycosin 
  
  
  
 [CHEBI:17821]
 thymine 
  
  
  
[CHEBI:18285]
 (S)-stylopine 
  
  
  
 [CHEBI:28777]
 liquiritigenin 
  
  
  
 [CHEBI:52086]
 glyceollin III 
  
  
  
[CHEBI:63558]
 DIBOA 
  
  
  
 [CHEBI:63559]
 HBOA 
  
  
  
 [CHEBI:65063]
 cyclo(L-tyrosyl-L-tyrosyl) 
  
  
  
[CHEBI:67153]
 (+)-larreatricin 
  
  
  
 [CHEBI:67154]
 (+)-3'-hydroxylarreatricin 
  
  
  
 [CHEBI:71596]
 mycocyclosin 
  
  
  
[CHEBI:72678]
 8-O-methyldihydrosterigmatocystin 
  
  
  

Acting on single donors with incorporation of molecular oxygen (oxygenases) [EC:1.13] (3)   
[CHEBI:2311]
 Oplophorus luciferin 
  
  
  
 [CHEBI:16531]
 Renilla luciferin 
  
  
  
 [CHEBI:17959]
 oxidized Renilla luciferin 
  
  
  

Acting on the aldehyde or oxo group of donors [EC:1.2] (1)   
[CHEBI:17310]
 pyridoxal 
  
  
  

Acting on the CH-CH group of donors [EC:1.3] (9)   
[CHEBI:15901]
 5,6-dihydrouracil 
  
  
  
 [CHEBI:16118]
 berberine 
  
  
  
 [CHEBI:16592]
 (S)-canadine 
  
  
  
[CHEBI:16786]
 vestitone 
  
  
  
 [CHEBI:17568]
 uracil 
  
  
  
 [CHEBI:17821]
 thymine 
  
  
  
[CHEBI:27468]
 5,6-dihydrothymine 
  
  
  
 [CHEBI:71608]
 cyclo(L-phenylalanyl-L-leucyl) 
  
  
  
 [CHEBI:71609]
 albonoursin 
  
  
  

Acting on the CH-NH group of donors [EC:1.5] (7)   
[CHEBI:15372]
 5,6,7,8-tetrahydrobiopterin 
  
  
  
 [CHEBI:15373]
 biopterin 
  
  
  
 [CHEBI:16118]
 berberine 
  
  
  
[CHEBI:16708]
 adenine 
  
  
  
 [CHEBI:17209]
 dihydrosanguinarine 
  
  
  
 [CHEBI:17789]
 dihydrochelirubine 
  
  
  
[CHEBI:28889]
 5,6,7,8-tetrahydropteridine 
  
  
  

Acting on the CH-OH group of donors [EC:1.1] (7)   
[CHEBI:16335]
 adenosine 
  
  
  
 [CHEBI:16786]
 vestitone 
  
  
  
 [CHEBI:17310]
 pyridoxal 
  
  
  
[CHEBI:17596]
 inosine 
  
  
  
 [CHEBI:17889]
 isopyridoxal 
  
  
  
 [CHEBI:59560]
 sapropterin 
  
  
  
[CHEBI:71634]
 hydroxyversicolorone 
  
  
  

Acting on X-H and Y-H to form an X-Y bond [EC:1.21] (2)   
[CHEBI:16118]
 berberine 
  
  
  
 [CHEBI:17129]
 (S)-scoulerine 
  
  
  

Reducing C-O-C group as acceptor [EC:1.23] (3)   
[CHEBI:40]
 (+)-pinoresinol 
  
  
  
 [CHEBI:67245]
 (-)-pinoresinol 
  
  
  
 [CHEBI:67246]
 (+)-lariciresinol