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

02. Food Pesticide Chemicals with Regulated Residues on Food Commodities

03. Biological Effects of Specific Chemicals (group results)
aetiopathogenetic uses [CHEBI:52209] (1)
biochemical uses [CHEBI:52206] (12)
biophysical uses [CHEBI:52208] (1)
molecular messenger [CHEBI:33280] (3)
pharmacological uses [CHEBI:52210] (2)
physiological uses [CHEBI:52211] (2)

04. Bioactive Capabilities of Specific Chemicals : all > Oxidoreductases [EC:1]
Acting on CH or CH2 groups [EC:1.17] (4)
Acting on other nitrogenous compounds as donors [EC:1.7] (3)
Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] (20)
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] (1)
Acting on the CH-CH group of donors [EC:1.3] (10)
Acting on the CH-NH group of donors [EC:1.5] (6)
Acting on the CH-NH2 group of donors [EC:1.4] (2)
Acting on the CH-OH group of donors [EC:1.1] (16)
Oxidising metal ions [EC:1.16] (3)

05. Industrial Uses (group results)
pharmaceutical [CHEBI:52217] (4)

06. Name of Biological Source of Chemical

07. Part of Biological Source of Chemical

08. Chemical Category: all > polyatomic entity [CHEBI:36357] > molecule [CHEBI:25367] > cyclic compound [CHEBI:33595] > aromatic compound [CHEBI:33655] > organic aromatic compound [CHEBI:33659] > heteroarene [CHEBI:33833] (group results)
azaarene [CHEBI:50893] (2)
imidazopyrimidine [CHEBI:35875] (17)
monocyclic heteroarene [CHEBI:38179] (8)
nucleobase-containing molecular entity [CHEBI:61120] (9)
polycyclic heteroarene [CHEBI:38180] (18)
pteridines [CHEBI:26373] (13)
tetrapyrrole [CHEBI:26932] (4)

09. Chemical Capabilities

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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] > cyclic compound [CHEBI:33595] > aromatic compound [CHEBI:33655] > organic aromatic compound [CHEBI:33659] > heteroarene [CHEBI:33833]
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62 items, grouped by 04. Bioactive Capabilities of Specific Chemicals  (view ungrouped items)

Acting on CH or CH2 groups [EC:1.17] (4)   
[CHEBI:17368]
 hypoxanthine 
  
  
  
 [CHEBI:17712]
 9H-xanthine 
  
  
  
 [CHEBI:27732]
 caffeine 
  
  
  
[CHEBI:691622]
 1,3,7-trimethyluric acid 
  
  
  

Acting on other nitrogenous compounds as donors [EC:1.7] (3)   
[CHEBI:15363]
 N-acetylindoxyl 
  
  
  
 [CHEBI:16050]
 N-acetylisatin 
  
  
  
 [CHEBI:18072]
 5-hydroxyisouric acid 
  
  
  

Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] (20)   
[CHEBI:15372]
 5,6,7,8-tetrahydrobiopterin 
  
  
  
 [CHEBI:15374]
 4a-hydroxytetrahydrobiopterin 
  
  
  
 [CHEBI:15375]
 D-erythro-7,8-dihydrobiopterin 
  
  
  
[CHEBI:15432]
 magnesium protoporphyrin 13-monomethyl ester 
  
  
  
 [CHEBI:16450]
 2'-deoxyuridine 
  
  
  
 [CHEBI:16704]
 uridine 
  
  
  
[CHEBI:16881]
 1H-indole 
  
  
  
 [CHEBI:17712]
 9H-xanthine 
  
  
  
 [CHEBI:18072]
 5-hydroxyisouric acid 
  
  
  
[CHEBI:18171]
 8-O-methylsterigmatocystin 
  
  
  
 [CHEBI:27543]
 9H-carbazole 
  
  
  
 [CHEBI:27660]
 pyrrole-2-carboxylate 
  
  
  
[CHEBI:28536]
 3-hydroxyindolin-2-one 
  
  
  
 [CHEBI:31697]
 indolin-2-one 
  
  
  
 [CHEBI:48991]
 7-methylxanthine 
  
  
  
[CHEBI:58565]
 5-hydroxyimidazole-4-acetate 
  
  
  
 [CHEBI:62210]
 5-hydroxypyrrole-2-carboxylate 
  
  
  
 [CHEBI:72678]
 8-O-methyldihydrosterigmatocystin 
  
  
  
[CHEBI:72760]
 tryprostatin B 
  
  
  
 [CHEBI:72762]
 6-hydroxytryprostatin B 
  
  
  

Acting on single donors with incorporation of molecular oxygen (oxygenases) [EC:1.13] (4)   
[CHEBI:16031]
 indole-3-acetamide 
  
  
  
 [CHEBI:16881]
 1H-indole 
  
  
  
 [CHEBI:17828]
 2,3-dihydroxyindole 
  
  
  
[CHEBI:30616]
 ATP(4-) 
  
  
  

Acting on the aldehyde or oxo group of donors [EC:1.2] (1)   
[CHEBI:18086]
 indol-3-ylacetaldehyde 
  
  
  

Acting on the CH-CH group of donors [EC:1.3] (10)   
[CHEBI:15333]
 zeatin 
  
  
  
 [CHEBI:16092]
 isoquinoline 
  
  
  
 [CHEBI:17319]
 5'-deoxyadenosine 
  
  
  
[CHEBI:17362]
 quinoline 
  
  
  
 [CHEBI:17397]
 3-methyloxindole 
  
  
  
 [CHEBI:17874]
 dihydrozeatin 
  
  
  
[CHEBI:17920]
 3-methyleneoxindole 
  
  
  
 [CHEBI:27247]
 urocanate 
  
  
  
 [CHEBI:30616]
 ATP(4-) 
  
  
  
[CHEBI:72991]
 dihydrourocanate 
  
  
  

Acting on the CH-NH group of donors [EC:1.5] (6)   
[CHEBI:15372]
 5,6,7,8-tetrahydrobiopterin 
  
  
  
 [CHEBI:15373]
 biopterin 
  
  
  
 [CHEBI:16708]
 adenine 
  
  
  
[CHEBI:17660]
 N(6)-dimethylallyladenine 
  
  
  
 [CHEBI:28889]
 5,6,7,8-tetrahydropteridine 
  
  
  
 [CHEBI:30156]
 6,7-dihydropteridine 
  
  
  

Acting on the CH-NH2 group of donors [EC:1.4] (2)   
[CHEBI:27398]
 imidazole-4-acetaldehyde 
  
  
  
 [CHEBI:58432]
 histaminium 
  
  
  

Acting on the CH-OH group of donors [EC:1.1] (16)   
[CHEBI:1958]
 5'-dehydroadenosine 
  
  
  
 [CHEBI:16095]
 sepiapterin 
  
  
  
 [CHEBI:16335]
 adenosine 
  
  
  
[CHEBI:17248]
 6-lactoyl-5,6,7,8-tetrahydropterin 
  
  
  
 [CHEBI:17319]
 5'-deoxyadenosine 
  
  
  
 [CHEBI:17596]
 inosine 
  
  
  
[CHEBI:17804]
 6-pyruvoyl-5,6,7,8-tetrahydropterin 
  
  
  
 [CHEBI:17890]
 tryptophol 
  
  
  
 [CHEBI:18086]
 indol-3-ylacetaldehyde 
  
  
  
[CHEBI:18385]
 thiamine(1+) 
  
  
  
 [CHEBI:27427]
 5'-dehydroinosine 
  
  
  
 [CHEBI:43029]
 L-erythro-7,8-dihydrobiopterin 
  
  
  
[CHEBI:57605]
 adenin-9-yl riburonosate(1-) 
  
  
  
 [CHEBI:59560]
 sapropterin 
  
  
  
 [CHEBI:64240]
 L-threo-7,8-dihydrobiopterin 
  
  
  
[CHEBI:64241]
 (6R)-L-threo-tetrahydrobiopterin 
  
  
  

Oxidising metal ions [EC:1.16] (3)   
[CHEBI:15852]
 aquacob(III)alamin 
  
  
  
 [CHEBI:16304]
 cob(II)alamin 
  
  
  
 [CHEBI:17439]
 cyanocob(III)alamin