Page last updated: 2024-12-07

ribose 1-phosphate

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

ribose 1-phosphate: RN given refers to (D)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

alpha-D-ribose 1-phosphate : The 1-phospho derivative of alpha-D-ribose. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID439236
CHEMBL ID603367
CHEBI ID16300
SCHEMBL ID1995711
MeSH IDM0098088

Synonyms (21)

Synonym
1-phospho-alpha-d-ribofuranose
CHEBI:16300 ,
1-o-phosphono-alpha-d-ribofuranose
alpha-d-ribofuranose 1-(dihydrogen phosphate)
r1p ,
ribose 1-phosphate
ribose-1-phosphate
C00620
alpha-d-ribose 1-phosphate
DB03101
CHEMBL603367
SCHEMBL1995711
YXJDFQJKERBOBM-TXICZTDVSA-N
{[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}phosphonic acid
d-ribofuranose 1-phosphate
a-d-ribofuranose 1-(dihydrogen phosphate)
d-ribose-1p
ribofuranose 1-phosphate
a-d-ribose 1-phosphate
ribose-1-phosphate; 1-o-phosphono-alpha-d-ribose; 1-o-phosphono-d-ribose; 1-o-phosphono-ribose
Q18213356
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
Escherichia coli metaboliteAny bacterial metabolite produced during a metabolic reaction in Escherichia coli.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (1)

ClassDescription
D-ribose 1-phosphateA ribose monophosphate that is D-ribose substituted at position 1 by a phosphate group.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (46)

PathwayProteinsCompounds
Nicotinate and Nicotinamide Metabolism1434
Pyrimidine Metabolism2353
Purine Metabolism3766
Pentose Phosphate Pathway1527
Adenosine Deaminase Deficiency3766
Adenylosuccinate Lyase Deficiency3766
Gout or Kelley-Seegmiller Syndrome3766
Lesch-Nyhan Syndrome (LNS)3766
Molybdenum Cofactor Deficiency3766
Xanthine Dehydrogenase Deficiency (Xanthinuria)3766
Purine Nucleoside Phosphorylase Deficiency3766
AICA-Ribosiduria3766
beta-Ureidopropionase Deficiency2353
UMP Synthase Deficiency (Orotic Aciduria)2353
Dihydropyrimidinase Deficiency2353
MNGIE (Mitochondrial Neurogastrointestinal Encephalopathy)2353
Azathioprine Action Pathway4782
Mercaptopurine Action Pathway4780
Thioguanine Action Pathway4781
Xanthinuria Type I3766
Xanthinuria Type II3766
Glucose-6-phosphate Dehydrogenase Deficiency1527
Ribose-5-phosphate Isomerase Deficiency1527
Transaldolase Deficiency1527
Adenine Phosphoribosyltransferase Deficiency (APRT)3766
Mitochondrial DNA Depletion Syndrome-33766
Myoadenylate Deaminase Deficiency3766
PRPP Biosynthesis38
Pyrimidine Ribonucleosides Degradation511
Adenine and Adenosine Salvage I412
Adenine and Adenosine Salvage II411
Guanine and Guanosine Salvage310
Purine Ribonucleosides Degradation717
Adenosine Nucleotides Degradation813
Mitochondrial DNA Depletion Syndrome3566
The impact of Nsp14 on metabolism (COVID-19 Disease Map)084
salvage pathways of purine nucleosides021
superpathway of ribose and deoxyribose phosphate degradation024
(deoxy)ribose phosphate degradation018
salvage pathways of adenine, hypoxanthine, and their nucleosides023
purine and pyrimidine metabolism032
superpathway of histidine, purine, and pyrimidine biosynthesis064
salvage pathways of guanine, xanthine, and their nucleosides017
salvage pathways of purine nucleosides I027
Ureide biosynthesis017
ureide biogenesis417

Bioassays (1)

Assay IDTitleYearJournalArticle
AID216549Effective concentration range of compound was determined in stimulating Vgamma9 / Vdelta2 T cell2003Bioorganic & medicinal chemistry letters, Apr-07, Volume: 13, Issue:7
Replacing the pyrophosphate group of HMB-PP by a diphosphonate function abrogates Its potential to activate human gammadelta T cells but does not lead to competitive antagonism.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (59)

TimeframeStudies, This Drug (%)All Drugs %
pre-199019 (32.20)18.7374
1990's15 (25.42)18.2507
2000's16 (27.12)29.6817
2010's7 (11.86)24.3611
2020's2 (3.39)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews2 (3.28%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other59 (96.72%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]