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CHEBI:17361 - CMP

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name CMP
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
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Formula C9H14N3O8P
Net Charge 0
Average Mass 323.19664
Monoisotopic Mass 323.052
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:10090) Source: BioModels - MODEL1507180067 See: PubMed
Escherichia coli (NCBI:562) 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 CMP (CHEBI:17361) has role Escherichia coli metabolite (CHEBI:76971)
CMP (CHEBI:17361) has role human metabolite (CHEBI:77746)
CMP (CHEBI:17361) has role mouse metabolite (CHEBI:75771)
CMP (CHEBI:17361) is a cytidine 5'-phosphate (CHEBI:23521)
CMP (CHEBI:17361) is a pyrimidine ribonucleoside 5'-monophosphate (CHEBI:39457)
CMP (CHEBI:17361) is conjugate acid of CMP(2−) (CHEBI:60377)
Incoming 2'-O-methylcytidine 5'-monophosphate (CHEBI:44666) has functional parent CMP (CHEBI:17361)
5-methylcytidine 5'-monophosphate (CHEBI:74725) has functional parent CMP (CHEBI:17361)
N3-methylcytidine 5'-monophosphate (CHEBI:75083) has functional parent CMP (CHEBI:17361)
N4-acetylcytidine 5'-monophosphate (CHEBI:75086) has functional parent CMP (CHEBI:17361)
N4-methylcytidine 5'-monophosphate (CHEBI:74778) has functional parent CMP (CHEBI:17361)
CMP-5'-phosphonoformic acid (CHEBI:131759) has functional parent CMP (CHEBI:17361)
CMP-sugar (CHEBI:20878) has functional parent CMP (CHEBI:17361)
cytidine 5'-phosphate 2',3'-cyclic phosphate (CHEBI:41473) has functional parent CMP (CHEBI:17361)
lysidine monophosphate (CHEBI:83661) has functional parent CMP (CHEBI:17361)
CMP(2−) (CHEBI:60377) is conjugate base of CMP (CHEBI:17361)
CMP 3'-end residue (CHEBI:53116) is substituent group from CMP (CHEBI:17361)
CMP 5'-end residue (CHEBI:53103) is substituent group from CMP (CHEBI:17361)
CMP residue (CHEBI:50308) is substituent group from CMP (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
Database Links Databases
C00055 KEGG COMPOUND
C5P PDBeChem
CMP MetaCyc
DB03403 DrugBank
G10621 KEGG GLYCAN
HMDB00095 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 Waiting for 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
18 April 2016