CHEBI:17202 - IMP

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ChEBI Name IMP ChEBI ID CHEBI:17202 Definition A purine ribonucleoside 5'-monophosphate having hypoxanthine as the nucleobase. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:43475, CHEBI:43418, CHEBI:43524, CHEBI:43528, CHEBI:43611, CHEBI:43563, CHEBI:47501, CHEBI:5849, CHEBI:12057, CHEBI:13372, CHEBI:14457, CHEBI:12063, CHEBI:13373, CHEBI:19271 Supplier Information ChemicalBook:CB7191961, ChemicalBook:CB3409949, eMolecules:882178 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License Inosinic acid or inosine monophosphate (IMP) is a nucleotide (that is, a nucleoside monophosphate). Widely used as a flavor enhancer, it is typically obtained from chicken byproducts or other meat industry waste. Inosinic acid is important in metabolism. It is the ribonucleotide of hypoxanthine and the first nucleotide formed during the synthesis of purine nucleotides. It can also be formed by the deamination of adenosine monophosphate by AMP deaminase. It can be hydrolysed to inosine. The enzyme deoxyribonucleoside triphosphate pyrophosphohydrolase, encoded by YJR069C in Saccharomyces cerevisiae and containing (d)ITPase and (d)XTPase activities, hydrolyzes inosine triphosphate (ITP) releasing pyrophosphate and IMP. Important derivatives of inosinic acid include the purine nucleotides found in nucleic acids and adenosine triphosphate, which is used to store chemical energy in muscle and other tissues. In the food industry, inosinic acid and its salts such as disodium inosinate are used as flavor enhancers. It is known as E number reference E630. Read full article at Wikipedia Formula C10H13N4O8P Net Charge 0 Average Mass 348.20600 Monoisotopic Mass 348.04710 InChI 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)/t4-,6-,7-,10-/m1/s1 InChIKey GRSZFWQUAKGDAV-KQYNXXCUSA-N SMILES O[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)n1cnc2c1nc[nH]c2=O Metabolite of Species Details Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed Escherichia coli (NCBI:txid562) See: PubMed Homo sapiens (NCBI:txid9606) See: PubMed Roles Classification Biological Role(s): Escherichia coli metabolite Any bacterial metabolite produced during a metabolic reaction in Escherichia coli. mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). View more via ChEBI Ontology ChEBI Ontology Outgoing IMP (CHEBI:17202) has role Escherichia coli metabolite (CHEBI:76971) IMP (CHEBI:17202) has role human metabolite (CHEBI:77746) IMP (CHEBI:17202) has role mouse metabolite (CHEBI:75771) IMP (CHEBI:17202) is a inosine phosphate (CHEBI:24843) IMP (CHEBI:17202) is a purine ribonucleoside 5'-monophosphate (CHEBI:37021) IMP (CHEBI:17202) is conjugate acid of IMP(2−) (CHEBI:58053) Incoming 2'-deoxyinosine-5'-diphosphate (CHEBI:28823) has functional parent IMP (CHEBI:17202) 2'-deoxyinosine-5'-monophosphate (CHEBI:28806) has functional parent IMP (CHEBI:17202) IMP(2−) (CHEBI:58053) is conjugate base of IMP (CHEBI:17202) IMP residue (CHEBI:76778) is substituent group from IMP (CHEBI:17202) IUPAC Name 5'-inosinic acid Synonyms Sources 2'-inosine-5'-monophosphate ChEBI 5'-IMP KEGG COMPOUND 5'-Inosinate KEGG COMPOUND 5'-Inosine monophosphate KEGG COMPOUND 5'-Inosinic acid KEGG COMPOUND hypoxanthosine 5'-monophosphate ChEBI IMP KEGG COMPOUND Inosine 5'-monophosphate KEGG COMPOUND Inosine 5'-phosphate KEGG COMPOUND Inosine monophosphate KEGG COMPOUND Inosinic acid KEGG COMPOUND inosinic acid PDBeChem ribosylhypoxanthine monophosphate MetaCyc Manual Xrefs Databases C00007224 KNApSAcK C00130 KEGG COMPOUND DB04566 DrugBank HMDB0000175 HMDB IMP PDBeChem IMP MetaCyc Inosinic_acid Wikipedia View more database links Registry Numbers Types Sources 131-99-7 CAS Registry Number ChemIDplus 528845 Gmelin Registry Number Gmelin 630517 Reaxys Registry Number Reaxys Citation Last Modified 27 January 2016