Page last updated: 2024-11-12

5-formylcytosine

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

Description

5-formylcytosine: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

5-formylcytosine : A nucleobase analogue that is cytosine in which the hydrogen at position 5 is replaced by a formyl group. [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 CID10986305
CHEBI ID76794
SCHEMBL ID1179741
MeSH IDM0560965

Synonyms (15)

Synonym
AKOS006360724
CHEBI:76794
4-amino-2-oxopyrimidine-5-carbaldehyde
cytosine-5-carbaldehyde
5-formylcytosine
4-amino-2-oxo-1,2-dihydropyrimidine-5-carbaldehyde
SCHEMBL1179741
4425-59-6
AKOS024124512
5-pyrimidinecarboxaldehyde, 4-amino-1,2-dihydro-2-oxo-
Q27146337
6-amino-2-oxo-1,2-dihydropyrimidine-5-carbaldehyde
6-amino-2-oxo-1h-pyrimidine-5-carbaldehyde
SB56778
DTXSID701336487
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
metaboliteAny intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
[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 (4)

ClassDescription
aminopyrimidineA member of the class of pyrimidines that is pyrimidine substituted by at least one amino group and its derivatives.
pyrimidoneA pyrimidine carrying one or more oxo substituents.
nucleobase analogueA molecule that can substitute for a normal nucleobase in nucleic acids.
heteroarenecarbaldehydeAn aldehyde in which a formyl group is located on a heteroarene.
[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 (3)

PathwayProteinsCompounds
Gene expression (Transcription)90249
Epigenetic regulation of gene expression11717
Oxidative demethylation of DNA49

Research

Studies (149)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's117 (78.52)24.3611
2020's32 (21.48)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 24.22

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index24.22 (24.57)
Research Supply Index5.02 (2.92)
Research Growth Index4.57 (4.65)
Search Engine Demand Index29.35 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (24.22)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews21 (14.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other129 (86.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]