Page last updated: 2024-11-08

5-hydroxymethyldeoxycytidine monophosphate

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

Description

5-hydroxymethyl-2'-deoxycytidine: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID169016
CHEMBL ID597779
SCHEMBL ID231959
MeSH IDM0188111

Synonyms (27)

Synonym
4-amino-1-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-5-(hydroxymethyl)pyrimidin-2-one
4-amino-1-(4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-hydroxymethyl-1h-pyrimidin-2-one
5-hydroxymethyldeoxycytidine monophosphate
5-hydroxymethyl-2'-deoxycytidine
5-(hydroxymethyl)deoxycytidine
5-(hydroxymethyl)-2'-deoxycytidine
cytidine, 2'-deoxy-5-(hydroxymethyl)-
CHEMBL597779
7226-77-9
4-amino-1-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-(hydroxymethyl)pyrimidin-2-one
hm-dcmp
SCHEMBL231959
AKOS022183455
5-hydroxymethyl-2??-deoxycytidine
J-700033
HMUOMFLFUUHUPE-XLPZGREQSA-N
4-amino-1-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-(hydroxymethyl)-1,2-dihydropyrimidin-2-one
AS-65435
mfcd09842113
4-amino-1-((2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-(hydroxymethyl)pyrimidin-2(1h)-one
1-(2-deoxypentofuranosyl)-5-(hydroxymethyl)-4-imino-1,4-dihydropyrimidin-2-ol
DTXSID50993019
D90265
5-hydroxymethyl-2 inverted exclamation mark -deoxycytidine
HY-131394
CS-0134009
PD017712
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (7)

Assay IDTitleYearJournalArticle
AID458878Antiviral activity against HIV1 LAI in human CEM-SS cells assessed as RT activity after 4 serial passages with uninfected cells by serial passage experiment2010Journal of medicinal chemistry, Feb-25, Volume: 53, Issue:4
5-Modified-2'-dU and 2'-dC as mutagenic anti HIV-1 proliferation agents: synthesis and activity.
AID458876Antiviral activity against HIV1 3B in human MT4 cells assessed as RT activity after 5 days by single passage assay2010Journal of medicinal chemistry, Feb-25, Volume: 53, Issue:4
5-Modified-2'-dU and 2'-dC as mutagenic anti HIV-1 proliferation agents: synthesis and activity.
AID458875Cytotoxicity against human CEM-SS cells by MTT assay2010Journal of medicinal chemistry, Feb-25, Volume: 53, Issue:4
5-Modified-2'-dU and 2'-dC as mutagenic anti HIV-1 proliferation agents: synthesis and activity.
AID458874Antiviral activity against HIV1 LAI in human CEM-SS cells assessed as RT activity after 5 days by single passage assay2010Journal of medicinal chemistry, Feb-25, Volume: 53, Issue:4
5-Modified-2'-dU and 2'-dC as mutagenic anti HIV-1 proliferation agents: synthesis and activity.
AID458879Antiviral activity against HIV1 LAI in human CEM-SS cells assessed as RT activity after 4 to 8 serial passages with uninfected cells by serial passage experiment2010Journal of medicinal chemistry, Feb-25, Volume: 53, Issue:4
5-Modified-2'-dU and 2'-dC as mutagenic anti HIV-1 proliferation agents: synthesis and activity.
AID1714494Displacement of sodium 5-(3-(8-(3-carboxy-N-hydroxyacrylamido)octyl)thioureido)-2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)benzoate from Naegleria Tet-1 at 5 mM incubated for 20 mins followed by sodium 5-(3-(8-(3-carboxy-N-hydroxyacrylamido)octyl)thioureido)-2-(62016ACS medicinal chemistry letters, Feb-11, Volume: 7, Issue:2
A Fluorescence Polarization Biophysical Assay for the Naegleria DNA Hydroxylase Tet1.
AID458877Cytotoxicity against human MT4 cells by MTT assay2010Journal of medicinal chemistry, Feb-25, Volume: 53, Issue:4
5-Modified-2'-dU and 2'-dC as mutagenic anti HIV-1 proliferation agents: synthesis and activity.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (26)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (3.85)18.2507
2000's1 (3.85)29.6817
2010's20 (76.92)24.3611
2020's4 (15.38)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.43

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 weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.43 (24.57)
Research Supply Index3.33 (2.92)
Research Growth Index5.76 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.43)

All Compounds (24.57)

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%
Other27 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]