CHEBI:16695 - uridine 5'-monophosphate

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ChEBI Name uridine 5'-monophosphate
ChEBI ID CHEBI:16695
Definition A pyrimidine ribonucleoside 5'-monophosphate having uracil as the nucleobase.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:46381, CHEBI:47721, CHEBI:46362, CHEBI:46382, CHEBI:46385, CHEBI:13509, CHEBI:9849, CHEBI:27231, CHEBI:13508
Supplier Information ZINC000002510048
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L-Tyrosine or tyrosine (symbol Tyr or Y) or 4-hydroxyphenylalanine is one of the 20 standard amino acids that are used by cells to synthesize proteins. It is a conditionally essential amino acid with a polar side group. The word "tyrosine" is from the Greek tyrós, meaning cheese, as it was first discovered in 1846 by German chemist Justus von Liebig in the protein casein from cheese. It is called tyrosyl when referred to as a functional group or side chain. While tyrosine is generally classified as a hydrophobic amino acid, it is more hydrophilic than phenylalanine. It is encoded by the codons UAC and UAU in messenger RNA. The one-letter symbol Y was assigned to tyrosine for being alphabetically nearest of those letters available. Note that T was assigned to the structurally simpler threonine, U was avoided for its similarity with V for valine, W was assigned to tryptophan, while X was reserved for undetermined or atypical amino acids. The mnemonic tYrosine was also proposed.
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Formula C9H13N2O9P
Net Charge 0
Average Mass 324.18136
Monoisotopic Mass 324.03587
InChI InChI=1S/C9H13N2O9P/c12-5-1-2-11(9(15)10-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18/h1-2,4,6-8,13-14H,3H2,(H,10,12,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1
InChIKey DJJCXFVJDGTHFX-XVFCMESISA-N
SMILES O[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)n1ccc(=O)[nH]c1=O
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 uridine 5'-monophosphate (CHEBI:16695) has role Escherichia coli metabolite (CHEBI:76971)
uridine 5'-monophosphate (CHEBI:16695) has role human metabolite (CHEBI:77746)
uridine 5'-monophosphate (CHEBI:16695) has role mouse metabolite (CHEBI:75771)
uridine 5'-monophosphate (CHEBI:16695) is a pyrimidine ribonucleoside 5'-monophosphate (CHEBI:39457)
uridine 5'-monophosphate (CHEBI:16695) is a uridine 5'-phosphate (CHEBI:27232)
uridine 5'-monophosphate (CHEBI:16695) is conjugate acid of uridine 5'-monophosphate(2−) (CHEBI:57865)
Incoming 2'-O-methyluridine 5'-monophosphate (CHEBI:44642) has functional parent uridine 5'-monophosphate (CHEBI:16695)
5,6-dihydrouridine 5'-monophosphate (CHEBI:74673) has functional parent uridine 5'-monophosphate (CHEBI:16695)
5-(2-methoxy-2-oxoethyl)uridine 5'-monophosphate (CHEBI:75650) has functional parent uridine 5'-monophosphate (CHEBI:16695)
5-aminomethyl-2-thiouridine 5'-monophosphate (CHEBI:74678) has functional parent uridine 5'-monophosphate (CHEBI:16695)
5-bromouridine 5'-monophosphate (CHEBI:47131) has functional parent uridine 5'-monophosphate (CHEBI:16695)
5-carboxymethylaminomethyl-2'-O-methyluridine 5'-monophosphate (CHEBI:74785) has functional parent uridine 5'-monophosphate (CHEBI:16695)
5-carboxymethylaminomethyluridine 5'-monophosphate (CHEBI:74782) has functional parent uridine 5'-monophosphate (CHEBI:16695)
5-fluorouridine 5'-monophosphate (CHEBI:40101) has functional parent uridine 5'-monophosphate (CHEBI:16695)
5-methylaminomethyl-2-thiouridine 5'-monophosphate (CHEBI:74680) has functional parent uridine 5'-monophosphate (CHEBI:16695)
6-oxouridine 5'-phosphate (CHEBI:41150) has functional parent uridine 5'-monophosphate (CHEBI:16695)
N3-methyluridine 5'-monophosphate (CHEBI:74773) has functional parent uridine 5'-monophosphate (CHEBI:16695)
O4'-(5'-uridylyl)-L-tyrosine (CHEBI:21989) has functional parent uridine 5'-monophosphate (CHEBI:16695)
ddhUMP (CHEBI:156340) has functional parent uridine 5'-monophosphate (CHEBI:16695)
sofosbuvir (CHEBI:85083) has functional parent uridine 5'-monophosphate (CHEBI:16695)
uracil octosyl acid 5'-phosphate (CHEBI:133866) has functional parent uridine 5'-monophosphate (CHEBI:16695)
uridine 5'-monophosphate(2−) (CHEBI:57865) is conjugate base of uridine 5'-monophosphate (CHEBI:16695)
UMP 3'-end residue (CHEBI:53120) is substituent group from uridine 5'-monophosphate (CHEBI:16695)
UMP 5'-end residue (CHEBI:53105) is substituent group from uridine 5'-monophosphate (CHEBI:16695)
uridine 5'-monophosphate residue (CHEBI:46470) is substituent group from uridine 5'-monophosphate (CHEBI:16695)
IUPAC Name
5'-uridylic acid
Synonyms Sources
5'-UMP ChemIDplus
5'Uridylic acid KEGG COMPOUND
pU CBN
pU ChEBI
UMP KEGG COMPOUND
uridine 5'-(dihydrogen phosphate) ChemIDplus
Uridine 5'-monophosphate KEGG COMPOUND
uridine 5'-phosphate ChemIDplus
uridine 5'-phosphoric acid ChemIDplus
Uridine monophosphate KEGG COMPOUND
URIDINE-5'-MONOPHOSPHATE PDBeChem
uridylate ChEBI
Uridylic acid KEGG COMPOUND
Manual Xrefs Databases
C00007311 KNApSAcK
C00105 KEGG COMPOUND
DB03685 DrugBank
HMDB0000288 HMDB
U5PrF10 PDBeChem
UMP MetaCyc
UrF10 PDBeChem
Uridine_monophosphate Wikipedia
View more database links
Registry Numbers Types Sources
310455 Gmelin Registry Number Gmelin
47486 Reaxys Registry Number Reaxys
58-97-9 CAS Registry Number ChemIDplus
Citations
Last Modified
05 December 2017