CHEBI:16082 - UDP-α-D-xylose

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ChEBI Name UDP-α-D-xylose
ChEBI ID CHEBI:16082
ChEBI ASCII Name UDP-alpha-D-xylose
Definition A UDP-sugar having α-xylose as the sugar component. It is an important metabolite in the nucleotide sugar metabolism in animals, plants, fungi, and bacteria.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:46260, CHEBI:13490, CHEBI:9813, CHEBI:22105
Supplier Information
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Formula C14H22N2O16P2
Net Charge 0
Average Mass 536.27580
Monoisotopic Mass 536.04446
InChI InChI=1S/C14H22N2O16P2/c17-5-3-28-13(11(22)8(5)19)31-34(26,27)32-33(24,25)29-4-6-9(20)10(21)12(30-6)16-2-1-7(18)15-14(16)23/h1-2,5-6,8-13,17,19-22H,3-4H2,(H,24,25)(H,26,27)(H,15,18,23)/t5-,6-,8+,9-,10-,11-,12-,13-/m1/s1
InChIKey DQQDLYVHOTZLOR-OCIMBMBZSA-N
SMILES O[C@@H]1CO[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)n2ccc(=O)[nH]c2=O)[C@H](O)[C@H]1O
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Roles Classification
Biological Role(s): fundamental metabolite
Any metabolite produced by all living cells.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing UDP-α-D-xylose (CHEBI:16082) has role fundamental metabolite (CHEBI:78675)
UDP-α-D-xylose (CHEBI:16082) is a UDP-sugar (CHEBI:17297)
UDP-α-D-xylose (CHEBI:16082) is conjugate acid of UDP-α-D-xylose(2−) (CHEBI:57632)
Incoming UDP-α-D-xylose(2−) (CHEBI:57632) is conjugate base of UDP-α-D-xylose (CHEBI:16082)
IUPAC Name
uridine 5'-[3-(α-D-xylopyranosyl) dihydrogen diphosphate]
Synonyms Sources
Udp xylose ChemIDplus
UDP-alpha-D-xylose KEGG COMPOUND
UDP-D-xylose KEGG COMPOUND
UDP-xylose ChEBI
UDP-xylose KEGG COMPOUND
UDPxylose KEGG COMPOUND
Uridine 5'-(trihydrogen diphosphate), P'-alpha-D-xylopyranosyl ester ChemIDplus
Uridine diphosphate xylose ChemIDplus
URIDINE-5'-DIPHOSPHATE-XYLOPYRANOSE PDBeChem
Manual Xrefs Databases
C00190 KEGG COMPOUND
G10613 KEGG GLYCAN
HMDB0001018 HMDB
UDX PDBeChem
View more database links
Registry Numbers Types Sources
101812 Reaxys Registry Number Reaxys
3616-06-6 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
12481102 PubMed citation Europe PMC
20847005 PubMed citation Europe PMC
22008417 PubMed citation Europe PMC
23053089 PubMed citation Europe PMC
24561591 PubMed citation Europe PMC
Last Modified
27 January 2016