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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]
(3)
02. Food Pesticide Chemicals with Regulated Residues on Food Commodities
03. Biological Effects of Specific Chemicals
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biochemical uses [CHEBI:52206]
(group results)
cofactor [CHEBI:23357]
(5)
enzyme inhibitor [CHEBI:23924]
(3)
metabolite [CHEBI:25212]
(61)
photobiochemical uses [CHEBI:52216]
(3)
04. Bioactive Capabilities of Specific Chemicals
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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]
(34)
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]
(4)
Acting on the CH-CH group of donors [EC:1.3]
(10)
Acting on the CH-NH group of donors [EC:1.5]
(7)
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]
(3)
Reducing C-O-C group as acceptor [EC:1.23]
(4)
05. Industrial Uses
(group results)
food additive [CHEBI:64047]
(2)
fragrance [CHEBI:48318]
(1)
pesticide [CHEBI:25944]
(1)
pharmaceutical [CHEBI:52217]
(15)
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
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polyatomic entity [CHEBI:36357]
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molecule [CHEBI:25367]
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cyclic compound [CHEBI:33595]
(group results)
aromatic compound [CHEBI:33655]
(36)
bicyclic compound [CHEBI:33636]
(18)
heterocyclic compound [CHEBI:5686]
(50)
homocyclic compound [CHEBI:33597]
(4)
monocyclic compound [CHEBI:33661]
(18)
organic cyclic compound [CHEBI:33832]
(67)
polycyclic compound [CHEBI:33635]
(41)
09. Chemical Capabilities
(group results)
antioxidant [CHEBI:22586]
(4)
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04. Bioactive Capabilities of Specific Chemicals
:
Oxidoreductases [EC:1]
×
08. Chemical Category
:
polyatomic entity [CHEBI:36357]
>
molecule [CHEBI:25367]
>
cyclic compound [CHEBI:33595]
×
03. Biological Effects of Specific Chemicals
:
biochemical uses [CHEBI:52206]
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68 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
[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]
(34)
[CHEBI:3900]
costunolide
[CHEBI:8602]
pseudobaptigenin
[CHEBI:9192]
solavetivone
[CHEBI:15372]
5,6,7,8-tetrahydrobiopterin
[CHEBI:15882]
phenol
[CHEBI:16415]
protopine
[CHEBI:16536]
orcinol
[CHEBI:16592]
(S)-canadine
[CHEBI:16704]
uridine
[CHEBI:16794]
scopolamine
[CHEBI:17129]
(S)-scoulerine
[CHEBI:17209]
dihydrosanguinarine
[CHEBI:17252]
17alpha-hydroxyprogesterone
[CHEBI:17281]
2-deoxy-D-ribono-1,4-lactone
[CHEBI:17568]
uracil
[CHEBI:17602]
4-aminophenol
[CHEBI:17712]
9H-xanthine
[CHEBI:17789]
dihydrochelirubine
[CHEBI:17793]
calycosin
[CHEBI:17821]
thymine
[CHEBI:17823]
calcitriol
[CHEBI:17933]
calcidiol
[CHEBI:18285]
(S)-stylopine
[CHEBI:28777]
liquiritigenin
[CHEBI:52086]
glyceollin III
[CHEBI:63558]
DIBOA
[CHEBI:63559]
HBOA
[CHEBI:63664]
taxusin
[CHEBI:63665]
7beta-hydroxytaxusin
[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]
(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]
(4)
[CHEBI:17169]
benzaldehyde
[CHEBI:17310]
pyridoxal
[CHEBI:17597]
4-hydroxybenzaldehyde
[CHEBI:18346]
vanillin
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
[CHEBI:16933]
ergosterol
[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]
(14)
[CHEBI:16335]
adenosine
[CHEBI:16786]
vestitone
[CHEBI:17069]
3-hydroxybenzyl alcohol
[CHEBI:17252]
17alpha-hydroxyprogesterone
[CHEBI:17310]
pyridoxal
[CHEBI:17596]
inosine
[CHEBI:17597]
4-hydroxybenzaldehyde
[CHEBI:17745]
coniferol
[CHEBI:17889]
isopyridoxal
[CHEBI:18346]
vanillin
[CHEBI:59560]
sapropterin
[CHEBI:63906]
cholest-5-en-3-one
[CHEBI:65004]
(-)-secoisolariciresinol
[CHEBI:71634]
hydroxyversicolorone
Acting on X-H and Y-H to form an X-Y bond [EC:1.21]
(3)
[CHEBI:16118]
berberine
[CHEBI:16159]
sulochrin
[CHEBI:17129]
(S)-scoulerine
Reducing C-O-C group as acceptor [EC:1.23]
(4)
[CHEBI:40]
(+)-pinoresinol
[CHEBI:65004]
(-)-secoisolariciresinol
[CHEBI:67245]
(-)-pinoresinol
[CHEBI:67246]
(+)-lariciresinol