CHEBI:17111 - 5-O-phosphono-α-D-ribofuranosyl diphosphate

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 5-O-phosphono-α-D-ribofuranosyl diphosphate
ChEBI ID CHEBI:17111
ChEBI ASCII Name 5-O-phosphono-alpha-D-ribofuranosyl diphosphate
Definition A derivative of α-D-ribose having a phosphate group at the 5-position and a diphosphate at the 1-position.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:12160, CHEBI:12159, CHEBI:2121, CHEBI:45139, CHEBI:20625
Supplier Information
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Formula C5H13O14P3
Net Charge 0
Average Mass 390.06960
Monoisotopic Mass 389.95182
InChI InChI=1S/C5H13O14P3/c6-3-2(1-16-20(8,9)10)17-5(4(3)7)18-22(14,15)19-21(11,12)13/h2-7H,1H2,(H,14,15)(H2,8,9,10)(H2,11,12,13)/t2-,3-,4-,5-/m1/s1
InChIKey PQGCEDQWHSBAJP-TXICZTDVSA-N
SMILES O[C@H]1[C@@H](O)[C@H](O[C@@H]1COP(O)(O)=O)OP(O)(=O)OP(O)(O)=O
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Arabidopsis thaliana (NCBI:txid3702) 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.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 5-O-phosphono-α-D-ribofuranosyl diphosphate (CHEBI:17111) has functional parent α-D-ribose (CHEBI:45506)
5-O-phosphono-α-D-ribofuranosyl diphosphate (CHEBI:17111) has role Escherichia coli metabolite (CHEBI:76971)
5-O-phosphono-α-D-ribofuranosyl diphosphate (CHEBI:17111) has role human metabolite (CHEBI:77746)
5-O-phosphono-α-D-ribofuranosyl diphosphate (CHEBI:17111) has role mouse metabolite (CHEBI:75771)
5-O-phosphono-α-D-ribofuranosyl diphosphate (CHEBI:17111) has role plant metabolite (CHEBI:76924)
5-O-phosphono-α-D-ribofuranosyl diphosphate (CHEBI:17111) is a 5-O-phosphono-D-ribofuranosyl diphosphate (CHEBI:48956)
5-O-phosphono-α-D-ribofuranosyl diphosphate (CHEBI:17111) is conjugate acid of 5-O-phosphonato-α-D-ribofuranosyl diphosphate(5−) (CHEBI:58017)
Incoming 5-O-phosphonato-α-D-ribofuranosyl diphosphate(5−) (CHEBI:58017) is conjugate base of 5-O-phosphono-α-D-ribofuranosyl diphosphate (CHEBI:17111)
IUPAC Name
5-O-phosphono-α-D-ribofuranose 1-(trihydrogen diphosphate)
Synonyms Sources
5-Phospho-alpha-D-ribose 1-diphosphate KEGG COMPOUND
5-Phosphoribosyl 1-pyrophosphate KEGG COMPOUND
5-Phosphoribosyl diphosphate KEGG COMPOUND
α-D-ribofuranose 5-(dihydrogen phosphate) 1-(trihydrogen diphosphate) ChemIDplus
ALPHA-PHOSPHORIBOSYLPYROPHOSPHORIC ACID PDBeChem
phosphoribosyl pyrophosphate ChemIDplus
phosphoribosylpyrophosphate ChEBI
PRib-PP CBN
PRPP KEGG COMPOUND
Manual Xrefs Databases
C00007296 KNApSAcK
C00119 KEGG COMPOUND
DB01632 DrugBank
HMDB0000280 HMDB
PRP PDBeChem
PRPP MetaCyc
View more database links
Registry Numbers Types Sources
60403 Reaxys Registry Number Reaxys
60403 Beilstein Registry Number Beilstein
7540-64-9 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
22264286 PubMed citation Europe PMC
23509005 PubMed citation Europe PMC
23734909 PubMed citation Europe PMC
Last Modified
27 January 2016