all items  in current results   Refine your search within these categories: 01. Food Nutrient & Dietary Chemicals (group results) Carbohydrate components (4) Lipid components [ChEBI:18059] (2) Nitrogen components (1) Phenolic components [ChEBI:15882] (4) Vitamins [ChEBI:26848] (3) 02. Food Pesticide Chemicals with Regulated Residues on Food Commodities 03. Biological Effects of Specific Chemicals: all > biochemical uses [CHEBI:52206] (group results) enzyme inhibitor [CHEBI:23924] (2) metabolite [CHEBI:25212] (37) photobiochemical uses [CHEBI:52216] (2) 04. Bioactive Capabilities of Specific Chemicals : all > Oxidoreductases [EC:1] Acting on a peroxide as acceptor [EC:1.11] (1) Acting on CH or CH2 groups [EC:1.17] (1) Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] (12) 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] (2) Acting on the CH-CH group of donors [EC:1.3] (2) Acting on the CH-NH group of donors [EC:1.5] (1) Acting on the CH-NH2 group of donors [EC:1.4] (2) Acting on the CH-OH group of donors [EC:1.1] (18) Acting on X-H and Y-H to form an X-Y bond [EC:1.21] (2) more... 05. Industrial Uses (group results) food additive [CHEBI:64047] (3) pesticide [CHEBI:25944] (1) pharmaceutical [CHEBI:52217] (9) solvent [CHEBI:46787] (3) 06. Name of Biological Source of Chemical (group results) Fungi, Yeasts, Molds and Mildews (2) Plantae (7) 07. Part of Biological Source of Chemical (group results) fungal structure [FS:0000000] (1) plant structure [PO:0009011] (6) unspecified structure [PO:0000004] (3) 08. Chemical Category: all > main group molecular entity [CHEBI:33579] > s-block molecular entity [CHEBI:33674] > hydrogen molecular entity [CHEBI:33608] > hydroxides [CHEBI:24651] (group results) organic hydroxy compound [CHEBI:33822] (37) oxoacid [CHEBI:24833] (3) 09. Chemical Capabilities (group results) antioxidant [CHEBI:22586] (2) 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] > s-block molecular entity [CHEBI:33674] > hydrogen molecular entity [CHEBI:33608] > hydroxides [CHEBI:24651] × 03. Biological Effects of Specific Chemicals: biochemical uses [CHEBI:52206] × 40 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 CH or CH2 groups [EC:1.17] (1)    [CHEBI:15600]   (+)-catechin               Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] (12)    [CHEBI:15882]   phenol               [CHEBI:16536]   orcinol               [CHEBI:17252]   17alpha-hydroxyprogesterone               [CHEBI:17823]   calcitriol               [CHEBI:17933]   calcidiol               [CHEBI:28777]   liquiritigenin               [CHEBI:30041]   taxa-4(20),11-dien-5alpha,13alpha-diol               [CHEBI:63558]   DIBOA               [CHEBI:63559]   HBOA               [CHEBI:63665]   7beta-hydroxytaxusin               [CHEBI:67153]   (+)-larreatricin               [CHEBI:71596]   mycocyclosin               Acting on single donors with incorporation of molecular oxygen (oxygenases) [EC:1.13] (4)    [CHEBI:2311]   Oplophorus luciferin               [CHEBI:16531]   Renilla luciferin               [CHEBI:17268]   myo-inositol               [CHEBI:18346]   vanillin               Acting on the aldehyde or oxo group of donors [EC:1.2] (2)    [CHEBI:17750]   glycine betaine               [CHEBI:18346]   vanillin               Acting on the CH-CH group of donors [EC:1.3] (2)    [CHEBI:16786]   vestitone               [CHEBI:16933]   ergosterol               Acting on the CH-NH group of donors [EC:1.5] (1)    [CHEBI:29985]   L-glutamate(1-)               Acting on the CH-NH2 group of donors [EC:1.4] (2)    [CHEBI:29985]   L-glutamate(1-)               [CHEBI:58359]   L-glutamine zwitterion               Acting on the CH-OH group of donors [EC:1.1] (18)    [CHEBI:15354]   choline               [CHEBI:16109]   propane-1,3-diol               [CHEBI:16236]   ethanol               [CHEBI:16786]   vestitone               [CHEBI:16813]   galactitol               [CHEBI:16899]   D-mannitol               [CHEBI:17069]   3-hydroxybenzyl alcohol               [CHEBI:17151]   xylitol               [CHEBI:17252]   17alpha-hydroxyprogesterone               [CHEBI:17268]   myo-inositol               [CHEBI:17745]   coniferol               [CHEBI:17750]   glycine betaine               [CHEBI:17754]   glycerol               [CHEBI:17924]   D-glucitol               [CHEBI:18346]   vanillin               [CHEBI:48300]   D-threitol               [CHEBI:65004]   (-)-secoisolariciresinol               [CHEBI:71634]   hydroxyversicolorone               Acting on X-H and Y-H to form an X-Y bond [EC:1.21] (2)    [CHEBI:16159]   sulochrin               [CHEBI:17750]   glycine betaine               Reducing C-O-C group as acceptor [EC:1.23] (4)    [CHEBI:40]   (+)-pinoresinol               [CHEBI:65004]   (-)-secoisolariciresinol               [CHEBI:67245]   (-)-pinoresinol               [CHEBI:67246]   (+)-lariciresinol