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01. Food Nutrient & Dietary Chemicals
(group results)
Carbohydrate components
(1)
Lipid components [ChEBI:18059]
(1)
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(1)
organosulfur compound [CHEBI:33261]
(1)
02. Food Pesticide Chemicals with Regulated Residues on Food Commodities
03. Biological Effects of Specific Chemicals
(group results)
aetiopathogenetic uses [CHEBI:52209]
(5)
antimicrobial agent [CHEBI:33281]
(1)
biochemical uses [CHEBI:52206]
(4)
osmolyte [CHEBI:25728]
(1)
pharmacological uses [CHEBI:52210]
(3)
04. Bioactive Capabilities of Specific Chemicals
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Oxidoreductases [EC:1]
Acting on a peroxide as acceptor [EC:1.11]
(1)
Acting on a sulfur group of donors [EC:1.8]
(2)
Acting on CH or CH2 groups [EC:1.17]
(1)
Acting on diphenols and related substances as donors [EC:1.10]
(1)
Acting on NADH or NADPH [EC:1.6]
(1)
Acting on other nitrogenous compounds as donors [EC:1.7]
(1)
Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14]
(5)
Acting on phosphorus or arsenic in donors [EC:1.20]
(1)
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]
(2)
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05. Industrial Uses
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solvent [CHEBI:46787]
(group results)
cyclohexanol [CHEBI:18099]
(1)
glycerol [CHEBI:17754]
(1)
non-polar solvent [CHEBI:48355]
(2)
polar solvent [CHEBI:48354]
(8)
06. Name of Biological Source of Chemical
07. Part of Biological Source of Chemical
08. Chemical Category
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inorganic molecular entity [CHEBI:24835]
(1)
main group molecular entity [CHEBI:33579]
(12)
polyatomic entity [CHEBI:36357]
(11)
09. Chemical Capabilities
(group results)
antioxidant [CHEBI:22586]
(1)
fuel additive [CHEBI:62803]
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[CHEBI:55394]
p-nitrophenylphosphocholine
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04. Bioactive Capabilities of Specific Chemicals
:
Oxidoreductases [EC:1]
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05. Industrial Uses
:
solvent [CHEBI:46787]
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12 items, grouped by
04. Bioactive Capabilities of Specific Chemicals
(
view ungrouped items
)
Acting on a peroxide as acceptor [EC:1.11]
(1)
[CHEBI:15377]
water
Acting on a sulfur group of donors [EC:1.8]
(2)
[CHEBI:15377]
water
[CHEBI:28262]
dimethyl sulfoxide
Acting on CH or CH2 groups [EC:1.17]
(1)
[CHEBI:15377]
water
Acting on diphenols and related substances as donors [EC:1.10]
(1)
[CHEBI:15377]
water
Acting on NADH or NADPH [EC:1.6]
(1)
[CHEBI:15377]
water
Acting on other nitrogenous compounds as donors [EC:1.7]
(1)
[CHEBI:15377]
water
Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14]
(5)
[CHEBI:15347]
acetone
[CHEBI:15377]
water
[CHEBI:16716]
benzene
[CHEBI:17578]
toluene
[CHEBI:17790]
methanol
Acting on phosphorus or arsenic in donors [EC:1.20]
(1)
[CHEBI:15377]
water
Acting on single donors with incorporation of molecular oxygen (oxygenases) [EC:1.13]
(1)
[CHEBI:15377]
water
Acting on the aldehyde or oxo group of donors [EC:1.2]
(2)
[CHEBI:15377]
water
[CHEBI:17790]
methanol
Acting on the CH-CH group of donors [EC:1.3]
(1)
[CHEBI:15377]
water
Acting on the CH-NH group of donors [EC:1.5]
(1)
[CHEBI:15377]
water
Acting on the CH-NH2 group of donors [EC:1.4]
(1)
[CHEBI:15377]
water
Acting on the CH-OH group of donors [EC:1.1]
(9)
[CHEBI:15347]
acetone
[CHEBI:15377]
water
[CHEBI:16109]
propane-1,3-diol
[CHEBI:16236]
ethanol
[CHEBI:16997]
propane-1,2-diol
[CHEBI:17754]
glycerol
[CHEBI:17790]
methanol
[CHEBI:17824]
propan-2-ol
[CHEBI:18099]
cyclohexanol
Acting on X-H and Y-H to form an X-Y bond [EC:1.21]
(1)
[CHEBI:15377]
water
Oxidising metal ions [EC:1.16]
(1)
[CHEBI:15377]
water
Reducing C-O-C group as acceptor [EC:1.23]
(1)
[CHEBI:15377]
water