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01. Food Nutrient & Dietary Chemicals
02. Food Pesticide Chemicals with Regulated Residues on Food Commodities
03. Biological Effects of Specific Chemicals
(group results)
biochemical uses [CHEBI:52206]
(4)
pharmacological uses [CHEBI:52210]
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04. Bioactive Capabilities of Specific Chemicals
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Oxidoreductases [EC:1]
Acting on a sulfur group of donors [EC:1.8]
(1)
Acting on hydrogen as donor [EC:1.12]
(1)
Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14]
(4)
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]
(1)
Acting on the CH-CH group of donors [EC:1.3]
(3)
Acting on the CH-NH group of donors [EC:1.5]
(1)
Acting on the CH-OH group of donors [EC:1.1]
(27)
05. Industrial Uses
(group results)
pharmaceutical [CHEBI:52217]
(1)
06. Name of Biological Source of Chemical
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main group molecular entity [CHEBI:33579]
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p-block molecular entity [CHEBI:33675]
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carbon group molecular entity [CHEBI:33582]
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organic molecular entity [CHEBI:50860]
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heteroorganic entity [CHEBI:33285]
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organochalcogen compound [CHEBI:36962]
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organooxygen compound [CHEBI:36963]
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carbohydrate derivative [CHEBI:63299]
(group results)
alditol derivative [CHEBI:63423]
(3)
amino sugar [CHEBI:28963]
(2)
carbohydrate lactone [CHEBI:37421]
(13)
carbohydrate phosphate [CHEBI:26816]
(6)
disaccharide derivative [CHEBI:63353]
(1)
monosaccharide derivative [CHEBI:63367]
(3)
N-glycosyl compound [CHEBI:21731]
(12)
09. Chemical Capabilities
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04. Bioactive Capabilities of Specific Chemicals
:
Oxidoreductases [EC:1]
×
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]
>
organochalcogen compound [CHEBI:36962]
>
organooxygen compound [CHEBI:36963]
>
carbohydrate derivative [CHEBI:63299]
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32 items, grouped by
04. Bioactive Capabilities of Specific Chemicals
(
view ungrouped items
)
Acting on a sulfur group of donors [EC:1.8]
(1)
[CHEBI:16768]
mycothiol
Acting on hydrogen as donor [EC:1.12]
(1)
[CHEBI:57922]
coenzyme gamma-F420-2(5-)
Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14]
(4)
[CHEBI:16450]
2'-deoxyuridine
[CHEBI:16704]
uridine
[CHEBI:16897]
D-erythrose 4-phosphate(2-)
[CHEBI:17281]
2-deoxy-D-ribono-1,4-lactone
Acting on single donors with incorporation of molecular oxygen (oxygenases) [EC:1.13]
(1)
[CHEBI:30616]
ATP(4-)
Acting on the aldehyde or oxo group of donors [EC:1.2]
(1)
[CHEBI:16897]
D-erythrose 4-phosphate(2-)
Acting on the CH-CH group of donors [EC:1.3]
(3)
[CHEBI:17319]
5'-deoxyadenosine
[CHEBI:17464]
L-galactono-1,4-lactone
[CHEBI:30616]
ATP(4-)
Acting on the CH-NH group of donors [EC:1.5]
(1)
[CHEBI:57922]
coenzyme gamma-F420-2(5-)
Acting on the CH-OH group of donors [EC:1.1]
(27)
[CHEBI:1958]
5'-dehydroadenosine
[CHEBI:15867]
D-xylono-1,5-lactone
[CHEBI:15895]
D-galactono-1,4-lactone
[CHEBI:15945]
D-galactono-1,5-lactone
[CHEBI:16217]
D-glucono-1,5-lactone
[CHEBI:16292]
D-arabinono-1,4-lactone
[CHEBI:16299]
dehydrocoformycin
[CHEBI:16335]
adenosine
[CHEBI:16768]
mycothiol
[CHEBI:17100]
L-arabinono-1,4-lactone
[CHEBI:17319]
5'-deoxyadenosine
[CHEBI:17464]
L-galactono-1,4-lactone
[CHEBI:17587]
L-gulono-1,4-lactone
[CHEBI:17596]
inosine
[CHEBI:17702]
D-apiitol
[CHEBI:17937]
L-rhamnono-1,4-lactone
[CHEBI:18118]
L-xylono-1,4-lactone
[CHEBI:18268]
D-glucurono-6,3-lactone
[CHEBI:20750]
6-phospho-2-dehydro-D-gluconate(3-)
[CHEBI:27427]
5'-dehydroinosine
[CHEBI:28745]
L-xylo-hex-3-ulonolactone
[CHEBI:44278]
N-acetyl-alpha-D-glucosamine
[CHEBI:57605]
adenin-9-yl riburonosate(1-)
[CHEBI:57922]
coenzyme gamma-F420-2(5-)
[CHEBI:58890]
2,5-diamino-6-(1-D-ribitylamino)pyrimidin-4(3H)-one 5'-phosphate(2-)
[CHEBI:59545]
2,5-diamino-6-(1-D-ribosylamino)pyrimidin-4(3H)-one 5'-phosphate(2-)
[CHEBI:506227]
N-acetyl-D-glucosamine