Page last updated: 2024-12-08

carboxyaminoimidazole ribotide

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

Description

carboxyaminoimidazole ribotide: reacts with alanosine to form antimetabolite; substrate for EC 4.1.1.21; structure in second source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID165388
CHEBI ID28413
SCHEMBL ID4359558
MeSH IDM0057716

Synonyms (37)

Synonym
5-amino-1-(5-o-phosphono-beta-d-ribofuranosyl)-1h-imidazole-4-carboxylic acid
CHEBI:28413
5-amino-1-(5-phospho-d-ribosyl)imidazole-4-carboxylic acid
C2R ,
5-aminoimidazole carboxilic acid ribonucleotice
5'phosphoribosyl-4-carboxy-5-aminoimidazole
4-carboxy-5-aminoimidazole ribonucleotide
carboxy-air
1h-imidazole-4-carboxylic acid, 5-amino-1-(5-o-phosphono-beta-d-ribofuranosyl)-
6001-14-5
imidazole-4-carboxilic acid-5-amino-1-beta-d-ribofuranosyl-5'-(dihydrogen phosphate)
aicor
carboxyaminoimidazole ribotide
5-aminoimidazole-4-carboxilic acid ribonucleotide
5-amino-4-carboxyimidazole ribonucleotide
C04751
5-amino-1-(5-phospho-d-ribosyl)imidazole-4-carboxylate
1-(5'-phosphoribosyl)-4-carboxy-5-aminoimidazole
1-(5-phospho-d-ribosyl)-5-amino-4-imidazolecarboxylate
1-(5'-phosphoribosyl)-5-amino-4-carboxyimidazole
1-(5'-phosphoribosyl)-5-amino-4-imidazolecarboxylate
5'-phosphoribosyl-5-amino-4-imidazolecarboxylate
5'-phosphoribosyl-4-carboxy-5-aminoimidazole
cair
SCHEMBL4359558
5-amino-1-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]imidazole-4-carboxylic acid
5ma501z5do ,
5-amino-4-imidazolecarboxylic acid ribonucleotide
unii-5ma501z5do
carboxyaminoimidazole ribonucleotide
5-amino-1-((2r,3r,4s,5r)-3,4-dihydroxy-5-(phosphonooxymethyl)-tetrahydrofuran-2-yl)-1h-imidazole-4-carboxylic acid
1h-imidazole-4-carboxylic acid, 5-amino-1-(5-o-phosphono-.beta.-d-ribofuranosyl)-
DTXSID50208716
5-amino-1-[(2r,3r,4s,5r)-3,4-dihydroxy-5-[(phosphonooxy)methyl]oxolan-2-yl]-1h-imidazole-4-carboxylic acid
cair; 4-carboxy-5-aminoimidazole ribonucleotide
Q2816671
A847932
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
Escherichia coli metaboliteAny bacterial metabolite produced during a metabolic reaction in Escherichia coli.
mouse metaboliteAny mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
[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 (3)

ClassDescription
aminoimidazoleAny member of the class of imidazoles carrying at least one amino substituent.
1-(phosphoribosyl)imidazole
imidazole-4-carboxylic acid
[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 (27)

PathwayProteinsCompounds
Purine Metabolism3766
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
Azathioprine Action Pathway4782
Mercaptopurine Action Pathway4780
Thioguanine Action Pathway4781
Xanthinuria Type I3766
Xanthinuria Type II3766
Adenine Phosphoribosyltransferase Deficiency (APRT)3766
Mitochondrial DNA Depletion Syndrome-33766
Myoadenylate Deaminase Deficiency3766
Purine Nucleotides De Novo Biosynthesis2945
Purine Nucleotides De Novo Biosynthesis 22945
Mitochondrial DNA Depletion Syndrome3566
Purine nucleotides and Nucleosides metabolism ( Purine nucleotides and Nucleosides metabolism )10577
5'-Phospho-ribosyl-5-amino-imidazole-4-carboxylic acid = 5'-Phospho-ribosyl-5-amino-imidazole + CO2 ( Purine nucleotides and Nucleosides metabolism )13
The impact of Nsp14 on metabolism (COVID-19 Disease Map)084
purine nucleotides de novo biosynthesis I039
superpathway of histidine, purine, and pyrimidine biosynthesis064
purine nucleotides de novo biosynthesis II033
Biochemical pathways: part I0466

Research

Studies (9)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (11.11)18.7374
1990's3 (33.33)18.2507
2000's2 (22.22)29.6817
2010's2 (22.22)24.3611
2020's1 (11.11)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%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other10 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]