Item 1 of 4 (back to results) next alpha,alpha-trehalose A trehalose in which both glucose residues have alpha-configuration at the anomeric carbon.

Current search: 04. Bioactive Capabilities of Specific Chemicals : Hydrolases [EC:3] > Acting on ester bonds [EC:3.1] × 01. Food Nutrient & Dietary Chemicals: Carbohydrate components × Select any link to see items in a related category. more general categories    information about this item 01. Food Nutrient & Dietary Chemicals  01. Food Nutrient & Dietary Chemicals  Carbohydrate components (31)   Sugars (5)   Disaccharides [ChEBI:36233] (4)   trehalose [ChEBI:16551] (1) 03. Biological Effects of Specific Chemicals  03. Biological Effects of Specific Chemicals  biochemical uses [CHEBI:52206] (3306)   metabolite [CHEBI:25212] (2692)   secondary metabolite [CHEBI:26619] (2225)   alpha,alpha-trehalose [CHEBI:16551] (1) 04. Bioactive Capabilities of Specific Chemicals   04. Bioactive Capabilities of Specific Chemicals  Transferases [EC:2] (1441)   Acyltransferases [EC:2.3] (299)   Transferring groups other than amino-acyl groups [EC:2.3.1] (266)   Trehalose O-mycolyltransferase [EC:2.3.1.122] (3)   alpha,alpha-trehalose [CHEBI:16551] (1)  Glycosyltransferases [EC:2.4] (334)   Hexosyltransferases [EC:2.4.1] (257)   Alpha,alpha-trehalose phosphorylase [EC:2.4.1.64] (3)   alpha,alpha-trehalose [CHEBI:16551] (1)  Alpha,alpha-trehalose phosphorylase (configuration-retaining) [EC:2.4.1.231] (3)   alpha,alpha-trehalose [CHEBI:16551] (1)  Alpha,alpha-trehalose synthase [EC:2.4.1.245] (5)   alpha,alpha-trehalose [CHEBI:16551] (1)  Hydrolases [EC:3] (824)   Acting on ester bonds [EC:3.1] (313)   Phosphoric monoester hydrolases [EC:3.1.3] (102)   Trehalose-phosphatase [EC:3.1.3.12] (3)   alpha,alpha-trehalose [CHEBI:16551] (1)  Glycosylases [EC:3.2] (112)   Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds [EC:3.2.1] (81)   Alpha,alpha-trehalase [EC:3.2.1.28] (4)   alpha,alpha-trehalose [CHEBI:16551] (1)  Isomerases [EC:5] (351)   Intramolecular transferases (mutases) [EC:5.4] (104)   Transferring Other Groups [EC:5.4.99] (56)   Maltose alpha-D-glucosyltransferase [EC:5.4.99.16] (2)   alpha,alpha-trehalose [CHEBI:16551] (1) 08. Chemical Category  08. Chemical Category  main group molecular entity [CHEBI:33579] (25650)   p-block molecular entity [CHEBI:33675] (25343)   chalcogen molecular entity [CHEBI:33304] (15225)   oxygen molecular entity [CHEBI:25806] (14414)   organooxygen compound [CHEBI:36963] (11352)   carbohydrate [CHEBI:16646] (742)   oligosaccharide [CHEBI:50699] (306)   disaccharide [CHEBI:36233] (131)   glycosyl glycoside [CHEBI:24407] (8)   trehalose [CHEBI:27082] (4)   alpha,alpha-trehalose [CHEBI:16551] (1)  organochalcogen compound [CHEBI:36962] (11874)   organooxygen compound [CHEBI:36963] (11352)   carbohydrate [CHEBI:16646] (742)   oligosaccharide [CHEBI:50699] (306)   disaccharide [CHEBI:36233] (131)   glycosyl glycoside [CHEBI:24407] (8)   trehalose [CHEBI:27082] (4)   alpha,alpha-trehalose [CHEBI:16551] (1)  carbon group molecular entity [CHEBI:33582] (23847)   organic molecular entity [CHEBI:50860] (23769)   heteroorganic entity [CHEBI:33285] (15197)   organochalcogen compound [CHEBI:36962] (11874)   organooxygen compound [CHEBI:36963] (11352)   carbohydrate [CHEBI:16646] (742)   oligosaccharide [CHEBI:50699] (306)   disaccharide [CHEBI:36233] (131)   glycosyl glycoside [CHEBI:24407] (8)   trehalose [CHEBI:27082] (4)   alpha,alpha-trehalose [CHEBI:16551] (1) ChEBI Compound Accession Identifier:   [CHEBI:16551] ChEBI Compound Description:   A trehalose in which both glucose residues have alpha-configuration at the anomeric carbon. ChEBI Compound Identification Number:   16551 ChEBI InChI Value:   InChI=1S/C12H22O11/c13-1-3-5(15)7(17)9(19)11(21-3)23-12-10(20)8(18)6(16)4(2-14)22-12/h3-20H,1-2H2/t3-,4-,5-,6-,7+,8+,9-,10-,11-,12-/m1/s1 ChEBI InChIKey Value:   HDTRYLNUVZCQOY-LIZSDCNHSA-N ChEBI Compound Name:   alpha,alpha-trehalose ChEBI SMILES Value:   OC[C@H]1O[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O ChEBI Substance ID:   8143512 ChEBI URL:   ChEBI:16551 ChemSpider ID:   7149 Ontomatica Chemical Accession Key (OnChAKey):   HDTRYLNUVZCQOY_LIZSDCNHSA_N_000_000000 PubChem Compound ID:   7427