Item 5 of 6 (back to results) previous next IMP(2-) "Dianion of inosine 5'-phosphate arising from deprotonation of the phosphate OH groups; major species at pH 7.3."

Current search: 04. Bioactive Capabilities of Specific Chemicals : Ligases [EC:6] > Forming carbon—nitrogen bonds [EC:6.3] > Other Carbon-Nitrogen Ligases [EC:6.3.4] > Adenylosuccinate synthase [EC:6.3.4.4] × Select any link to see items in a related category. more general categories    information about this item 04. Bioactive Capabilities of Specific Chemicals   04. Bioactive Capabilities of Specific Chemicals  Oxidoreductases [EC:1] (1697)   Acting on the CH-OH group of donors [EC:1.1] (576)   With NAD or NADP as acceptor [EC:1.1.1] (507)   IMP dehydrogenase [EC:1.1.1.205] (6)   IMP(2-) [CHEBI:58053] (1)  Acting on other nitrogenous compounds as donors [EC:1.7] (34)   With NAD or NADP as acceptor [EC:1.7.1] (25)   GMP reductase [EC:1.7.1.7] (6)   IMP(2-) [CHEBI:58053] (1)  Transferases [EC:2] (1441)   Glycosyltransferases [EC:2.4] (334)   Pentosyltransferases [EC:2.4.2] (79)   Hypoxanthine phosphoribosyltransferase [EC:2.4.2.8] (6)   IMP(2-) [CHEBI:58053] (1)  Transferring phosphorus-containing groups [EC:2.7] (369)   Phosphotransferases with an alcohol group as acceptor [EC:2.7.1] (217)   Inosine kinase [EC:2.7.1.73] (5)   IMP(2-) [CHEBI:58053] (1)  Hydrolases [EC:3] (824)   Glycosylases [EC:3.2] (112)   Hydrolysing N-glycosyl compounds [EC:3.2.2] (33)   Inosinate nucleosidase [EC:3.2.2.12] (4)   IMP(2-) [CHEBI:58053] (1)  Acting on carbon-nitrogen bonds, other than peptide bonds [EC:3.5] (303)   In cyclic amidines [EC:3.5.4] (59)   AMP deaminase [EC:3.5.4.6] (5)   IMP(2-) [CHEBI:58053] (1)  IMP cyclohydrolase [EC:3.5.4.10] (3)   IMP(2-) [CHEBI:58053] (1)  Adenosine-phosphate deaminase [EC:3.5.4.17] (5)   IMP(2-) [CHEBI:58053] (1)  Acting on acid anhydrides [EC:3.6] (90)   In phosphorus-containing anhydrides [EC:3.6.1] (66)   Inosine diphosphate phosphatase [EC:3.6.1.64] (6)   IMP(2-) [CHEBI:58053] (1)  Ligases [EC:6] (206)   Forming carbon—nitrogen bonds [EC:6.3] (134)   Other Carbon-Nitrogen Ligases [EC:6.3.4] (44)   Adenylosuccinate synthase [EC:6.3.4.4] (6)   IMP(2-) [CHEBI:58053] (1) 08. Chemical Category  08. Chemical Category  ion [CHEBI:24870] (4391)   anion [CHEBI:22563] (3454)   organic anion [CHEBI:25696] (3155)   organophosphate oxoanion [CHEBI:58945] (1108)   IMP(2-) [CHEBI:58053] (1)  organic ion [CHEBI:25699] (3577)   organic anion [CHEBI:25696] (3155)   organophosphate oxoanion [CHEBI:58945] (1108)   IMP(2-) [CHEBI:58053] (1)  main group molecular entity [CHEBI:33579] (25650)   p-block molecular entity [CHEBI:33675] (25343)   pnictogen molecular entity [CHEBI:33302] (10027)   phosphorus molecular entity [CHEBI:26082] (2769)   phosphorus oxoacids and derivatives [CHEBI:36360] (2691)   phosphorus oxoacid derivative [CHEBI:36359] (2628)   phosphoric acid derivative [CHEBI:26079] (2611)   organophosphate oxoanion [CHEBI:58945] (1108)   IMP(2-) [CHEBI:58053] (1)  carbon group molecular entity [CHEBI:33582] (23847)   organic molecular entity [CHEBI:50860] (23769)   organic ion [CHEBI:25699] (3577)   organic anion [CHEBI:25696] (3155)   organophosphate oxoanion [CHEBI:58945] (1108)   IMP(2-) [CHEBI:58053] (1)  polyatomic entity [CHEBI:36357] (18777)   heteroatomic molecular entity [CHEBI:37577] (13672)   oxoacid derivative [CHEBI:33241] (3254)   phosphorus oxoacid derivative [CHEBI:36359] (2628)   phosphoric acid derivative [CHEBI:26079] (2611)   organophosphate oxoanion [CHEBI:58945] (1108)   IMP(2-) [CHEBI:58053] (1) ChEBI Compound Accession Identifier:   [CHEBI:58053] ChEBI Compound Description:   "Dianion of inosine 5'-phosphate arising from deprotonation of the phosphate OH groups; major species at pH 7.3." ChEBI Compound Identification Number:   58053 ChEBI InChI Value:   InChI=1S/C10H13N4O8P/c15-6-4(1-21-23(18,19)20)22-10(7(6)16)14-3-13-5-8(14)11-2-12-9(5)17/h2-4,6-7,10,15-16H,1H2,(H,11,12,17)(H2,18,19,20)/p-2/t4-,6-,7-,10-/m1/s1 ChEBI InChIKey Value:   GRSZFWQUAKGDAV-KQYNXXCUSA-L ChEBI Compound Name:   IMP(2-) ChEBI SMILES Value:   O[C@@H]1[C@@H](COP([O-])([O-])=O)O[C@H]([C@@H]1O)n1cnc2c1nc[nH]c2=O ChEBI Substance ID:   103158359 ChEBI URL:   ChEBI:58053 ChemSpider ID:   5482599 Ontomatica Chemical Accession Key (OnChAKey):   GRSZFWQUAKGDAV_KQYNXXCUSA_L_000_000000 PubChem Compound ID:   7140378