CHEBI:17361 - cytidine 5'-monophosphate

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ChEBI Name cytidine 5'-monophosphate ChEBI ID CHEBI:17361 Definition A pyrimidine ribonucleoside 5'-monophosphate having cytosine as the nucleobase. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:41312, CHEBI:41319, CHEBI:41691, CHEBI:41666, CHEBI:47362, CHEBI:48799, CHEBI:3275, CHEBI:13274, CHEBI:23520 Supplier Information ChemicalBook:CB6214708, eMolecules:509332, Selleckchem:Ellagic-acid, ZINC000003872446 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C9H14N3O8P Net Charge 0 Average Mass 323.19664 Monoisotopic Mass 323.05185 InChI InChI=1S/C9H14N3O8P/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18/h1-2,4,6-8,13-14H,3H2,(H2,10,11,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1 InChIKey IERHLVCPSMICTF-XVFCMESISA-N SMILES Nc1ccn([C@@H]2O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]2O)c(=O)n1 Metabolite of Species Details Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed Escherichia coli (NCBI:txid562) 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 cytidine 5'-monophosphate (CHEBI:17361) has role Escherichia coli metabolite (CHEBI:76971) cytidine 5'-monophosphate (CHEBI:17361) has role human metabolite (CHEBI:77746) cytidine 5'-monophosphate (CHEBI:17361) has role mouse metabolite (CHEBI:75771) cytidine 5'-monophosphate (CHEBI:17361) is a cytidine 5'-phosphate (CHEBI:23521) cytidine 5'-monophosphate (CHEBI:17361) is a pyrimidine ribonucleoside 5'-monophosphate (CHEBI:39457) cytidine 5'-monophosphate (CHEBI:17361) is conjugate acid of cytidine 5'-monophosphate(2−) (CHEBI:60377) Incoming 2'-O-methylcytidine 5'-monophosphate (CHEBI:44666) has functional parent cytidine 5'-monophosphate (CHEBI:17361) 5-methylcytidine 5'-monophosphate (CHEBI:74725) has functional parent cytidine 5'-monophosphate (CHEBI:17361) N3-methylcytidine 5'-monophosphate (CHEBI:75083) has functional parent cytidine 5'-monophosphate (CHEBI:17361) N4-acetylcytidine 5'-monophosphate (CHEBI:75086) has functional parent cytidine 5'-monophosphate (CHEBI:17361) N4-methylcytidine 5'-monophosphate (CHEBI:74778) has functional parent cytidine 5'-monophosphate (CHEBI:17361) CMP-5'-phosphonoformic acid (CHEBI:131759) has functional parent cytidine 5'-monophosphate (CHEBI:17361) CMP-sugar (CHEBI:20878) has functional parent cytidine 5'-monophosphate (CHEBI:17361) cytidine 5'-phosphate 2',3'-cyclic phosphate (CHEBI:41473) has functional parent cytidine 5'-monophosphate (CHEBI:17361) ddhCMP (CHEBI:156339) has functional parent cytidine 5'-monophosphate (CHEBI:17361) lysidine monophosphate (CHEBI:83661) has functional parent cytidine 5'-monophosphate (CHEBI:17361) cytidine 5'-monophosphate(2−) (CHEBI:60377) is conjugate base of cytidine 5'-monophosphate (CHEBI:17361) CMP 3'-end residue (CHEBI:53116) is substituent group from cytidine 5'-monophosphate (CHEBI:17361) CMP 5'-end residue (CHEBI:53103) is substituent group from cytidine 5'-monophosphate (CHEBI:17361) cytidine 5'-monophosphate residue (CHEBI:50308) is substituent group from cytidine 5'-monophosphate (CHEBI:17361) IUPAC Name 5'-cytidylic acid Synonyms Sources CMP KEGG COMPOUND cytidine 5'-monophosphate ChEBI Cytidine-5'-monophosphate KEGG COMPOUND cytidylate ChEBI Cytidylic acid KEGG COMPOUND pC ChEBI Manual Xrefs Databases C00055 KEGG COMPOUND C5P PDBeChem CMP MetaCyc DB03403 DrugBank G10621 KEGG GLYCAN HMDB0000095 HMDB View more database links Registry Numbers Types Sources 46982 Reaxys Registry Number Reaxys 63-37-6 CAS Registry Number KEGG COMPOUND 63-37-6 CAS Registry Number ChemIDplus Citations Types Sources 21968653 PubMed citation Europe PMC 22991951 PubMed citation Europe PMC 24053133 PubMed citation Europe PMC 2559771 PubMed citation Europe PMC Last Modified 16 November 2017