all items  in current results   Refine your search within these categories: 01. Food Nutrient & Dietary Chemicals (group results) Carbohydrate components (5) Lipid components [ChEBI:18059] (3) Nitrogen components (2) Phenolic components [ChEBI:15882] (5) Vitamins [ChEBI:26848] (2) 02. Food Pesticide Chemicals with Regulated Residues on Food Commodities 03. Biological Effects of Specific Chemicals: all > biochemical uses [CHEBI:52206] > metabolite [CHEBI:25212] > secondary metabolite [CHEBI:26619] (group results) (+)-3'-hydroxylarreatricin [CHEBI:67154] (1) (+)-5-epi-aristolochene [CHEBI:23925] (1) (+)-catechin [CHEBI:15600] (1) (+)-lariciresinol [CHEBI:67246] (1) (+)-larreatricin [CHEBI:67153] (1) (+)-pinoresinol [CHEBI:40] (1) (-)-pinoresinol [CHEBI:67245] (1) (-)-secoisolariciresinol [CHEBI:65004] (1) (3,4-dimethoxyphenyl)methanol [CHEBI:62150] (1) (6S)-dehydrovomifoliol [CHEBI:4372] (1) more... 04. Bioactive Capabilities of Specific Chemicals : all > Oxidoreductases [EC:1] Acting on a peroxide as acceptor [EC:1.11] (1) Acting on a sulfur group of donors [EC:1.8] (1) Acting on CH or CH2 groups [EC:1.17] (8) Acting on diphenols and related substances as donors [EC:1.10] (1) Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] (40) Acting on single donors with incorporation of molecular oxygen (oxygenases) [EC:1.13] (6) Acting on the aldehyde or oxo group of donors [EC:1.2] (9) Acting on the CH-CH group of donors [EC:1.3] (14) Acting on the CH-NH group of donors [EC:1.5] (5) Acting on the CH-NH2 group of donors [EC:1.4] (4) more... 05. Industrial Uses (group results) anti-inflammatory agent [CHEBI:67079] (1) food additive [CHEBI:64047] (4) pesticide [CHEBI:25944] (1) pharmaceutical [CHEBI:52217] (14) solvent [CHEBI:46787] (4) 06. Name of Biological Source of Chemical (group results) Archaea, Cyanobacteria and Bacteria (1) Fungi, Yeasts, Molds and Mildews (2) Plantae (17) 07. Part of Biological Source of Chemical (group results) fungal structure [FS:0000000] (1) plant structure [PO:0009011] (13) unspecified structure [PO:0000004] (10) 08. Chemical Category: all > main group molecular entity [CHEBI:33579] > p-block molecular entity [CHEBI:33675] (group results) carbon group molecular entity [CHEBI:33582] (92) chalcogen molecular entity [CHEBI:33304] (70) pnictogen molecular entity [CHEBI:33302] (29) 09. Chemical Capabilities (group results) antioxidant [CHEBI:22586] (5) Recently Viewed Items Go to Item History

These terms define your current search. Click the × to remove a term. 04. Bioactive Capabilities of Specific Chemicals : Oxidoreductases [EC:1] × 08. Chemical Category: main group molecular entity [CHEBI:33579] > p-block molecular entity [CHEBI:33675] × 03. Biological Effects of Specific Chemicals: biochemical uses [CHEBI:52206] > metabolite [CHEBI:25212] > secondary metabolite [CHEBI:26619] × 93 items, grouped by 04. Bioactive Capabilities of Specific Chemicals  (view ungrouped items) Acting on a peroxide as acceptor [EC:1.11] (1)    [CHEBI:62150]   (3,4-dimethoxyphenyl)methanol               Acting on a sulfur group of donors [EC:1.8] (1)    [CHEBI:16189]   sulfate               Acting on CH or CH2 groups [EC:1.17] (8)    [CHEBI:15600]   (+)-catechin               [CHEBI:17368]   hypoxanthine               [CHEBI:17568]   uracil               [CHEBI:17597]   4-hydroxybenzaldehyde               all 8 items... Acting on diphenols and related substances as donors [EC:1.10] (1)    [CHEBI:27547]   zeaxanthin               Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] (40)    [CHEBI:3900]   costunolide               [CHEBI:8602]   pseudobaptigenin               [CHEBI:9192]   solavetivone               [CHEBI:15347]   acetone               all 40 items... Acting on single donors with incorporation of molecular oxygen (oxygenases) [EC:1.13] (6)    [CHEBI:15740]   formate               [CHEBI:16810]   2-oxoglutarate(2-)               [CHEBI:17268]   myo-inositol               [CHEBI:18346]   vanillin               all 6 items... Acting on the aldehyde or oxo group of donors [EC:1.2] (9)    [CHEBI:15361]   pyruvate               [CHEBI:15740]   formate               [CHEBI:16424]   phenylacetaldehyde               [CHEBI:16810]   2-oxoglutarate(2-)               all 9 items... Acting on the CH-CH group of donors [EC:1.3] (14)    [CHEBI:15440]   squalene               [CHEBI:15901]   5,6-dihydrouracil               [CHEBI:16118]   berberine               [CHEBI:16592]   (S)-canadine               all 14 items... Acting on the CH-NH group of donors [EC:1.5] (5)    [CHEBI:15361]   pyruvate               [CHEBI:15373]   biopterin               [CHEBI:16118]   berberine               [CHEBI:16708]   adenine               all 5 items... Acting on the CH-NH2 group of donors [EC:1.4] (4)    [CHEBI:15361]   pyruvate               [CHEBI:16424]   phenylacetaldehyde               [CHEBI:16810]   2-oxoglutarate(2-)               [CHEBI:58359]   L-glutamine zwitterion               Acting on the CH-OH group of donors [EC:1.1] (37)    [CHEBI:4167]   D-glucopyranose               [CHEBI:4208]   D-mannopyranose               [CHEBI:4372]   (6S)-dehydrovomifoliol               [CHEBI:15347]   acetone               all 37 items... 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] (4)    [CHEBI:40]   (+)-pinoresinol               [CHEBI:65004]   (-)-secoisolariciresinol               [CHEBI:67245]   (-)-pinoresinol               [CHEBI:67246]   (+)-lariciresinol