Page last updated: 2024-10-15

cyclic imp

Description

Cyclic IMP: Inosine cyclic 3',5'-(hydrogen phosphate). An inosine nucleotide which acts as a mild inhibitor of the hydrolysis of cyclic AMP and cyclic GMP and as an inhibitor of cat heart cyclic AMP phosphodiesterase. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

3',5'-cyclic IMP : A 3',5'-cyclic purine nucleotide having hypoxanthine as the nucleobase. [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 CID135398663
CHEBI ID27541
MeSH IDM0011367

Synonyms (29)

Synonym
C00943
3',5'-cyclic imp
inosine 3',5'-cyclic monophosphate
cyclic imp
3545-76-4
inosine cyclic 3',5'-(hydrogen phosphate)
CHEBI:27541
inosine 3',5'-(hydrogen phosphate)
inosine-3',5'-cyclic-monophosphate
2sx2bu5nzp ,
unii-2sx2bu5nzp
inosine, cyclic 3',5'-(hydrogen phosphate)
einecs 222-593-7
41092-64-2
cimp
inosine-3',5'-cyclic-monophosphate free acid
W-202452
inosine-3',5'-cyclic phosphate
6sw ,
inosine-3',5'-cyclic monophosphate
cyclic 3',5'-imp
Q27103185
DTXSID00956856
2,7-dihydroxy-6-(6-hydroxy-9h-purin-9-yl)tetrahydro-2h,4h-2lambda~5~-furo[3,2-d][1,3,2]dioxaphosphinin-2-one
inosine cyclophosphate
inosine, cyclic 3',5'-phosphate
cyclic 3',5'-inosinic acid
3',5'-imp
9-((4ar,6r,7r,7as)-2,7-dihydroxy-2-oxo-4a,6,7,7a-tetrahydro-4h-furo(3,2-d)(1,3,2)dioxaphosphinin-6-yl)-3h-purin-6-one
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
mammalian metaboliteAny animal metabolite produced during a metabolic reaction in mammals.
Saccharomyces cerevisiae metaboliteAny fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae).
[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 (2)

ClassDescription
3',5'-cyclic purine nucleotide
nucleoside 3',5'-cyclic phosphateA ribosyl or deoxyribosyl derivative of a pyrimidine or purine base in which C-3 and C-5 of the ribose ring are engaged in formation of a cyclic mono-, di-, tri- or tetra-phosphate.
[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]

Research

Studies (80)

TimeframeStudies, This Drug (%)All Drugs %
pre-199046 (57.50)18.7374
1990's10 (12.50)18.2507
2000's4 (5.00)29.6817
2010's18 (22.50)24.3611
2020's2 (2.50)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%
Reviews5 (6.25%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other75 (93.75%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]