Page last updated: 2024-11-07

1-methylpseudouridine

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

Description

1-methylpseudouridine (m1Ψ) is a modified nucleoside found in various RNA molecules, including ribosomal RNA (rRNA) and transfer RNA (tRNA). It is a derivative of pseudouridine, where a methyl group is attached to the N1 position of the pseudouridine base. m1Ψ is known to play significant roles in RNA structure, stability, and function. Studies have shown that m1Ψ can enhance the stability of RNA molecules by increasing their resistance to degradation. This is because the methyl group can contribute to stacking interactions within the RNA structure, making the molecule more rigid and less susceptible to enzymatic breakdown. Additionally, m1Ψ has been implicated in influencing RNA folding and the formation of specific RNA structures, such as stem-loop structures. This, in turn, can affect the interactions of RNA molecules with other cellular components, including proteins and other RNA molecules. The presence of m1Ψ in rRNA has been linked to proper ribosome assembly and function. It can affect the efficiency of translation, the process of protein synthesis. Moreover, m1Ψ has been shown to be involved in regulating the activity of certain enzymes that interact with RNA. These enzymes include RNA-dependent RNA polymerases, which play a crucial role in the replication of viral RNA. The synthesis of m1Ψ is catalyzed by specific enzymes called methyltransferases. These enzymes specifically recognize and methylate pseudouridine residues within RNA molecules. The process typically involves the transfer of a methyl group from a donor molecule, such as S-adenosyl methionine (SAM), to the N1 position of the pseudouridine base. The study of m1Ψ is important for understanding the complex mechanisms underlying RNA biology and the roles of RNA modifications in cellular processes. Research on m1Ψ is ongoing, aiming to elucidate its specific functions in different RNA molecules, its potential therapeutic applications, and its implications for human health.'

1-methylpseudouridine: metabolite from culture filtrates of Streptomyces platensis; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

1-methylpseudouridine : A methylpseudouridine in which the methyl group is located at position N-1 on the uracil ring. [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 CID99543
CHEBI ID19068
SCHEMBL ID63879
MeSH IDM0061491

Synonyms (40)

Synonym
nsc-240023
13860-38-3
1-methylpseudouridine
5-[(2s,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1-methylpyrimidine-2,4-dione
n1-methyl-pseudouridine
09rad4m6wf ,
unii-09rad4m6wf
nsc 240023
m(1)f
(1s)-1,4-anhydro-1-(1-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)-d-ribitol
CHEBI:19068
SCHEMBL63879
uracil, 1-methyl-5-.beta.-d-ribofuranosyl-
n1-methylpseudouridine ,
DTXSID50160724
u-50228
AKOS030241474
1-n-me-pseudouridine
2,4(1h,3h)-pyrimidinedione, 1-methyl-5-.beta.-d-ribofuranosyl-
M3387
u 50228
5-((2s,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-1-methylpyrimidine-2,4(1h,3h)-dione
mfcd10687017
1-n-methyl-pseudouridine
Q27109108
HY-112582
CS-0047598
BS-51848
1-methyl-pseudouridine
A903408
8IZ ,
5-[(2s,3r,4s,5r)-5-(hydroxymethyl)-3,4-bis(oxidanyl)oxolan-2-yl]-1-methyl-pyrimidine-2,4-dione
PD156923
1-methyl-5-beta-d-ribofuranosyl-2,4(1h,3h)-pyrimidinedione
m1psi
(1s)-1,4-anhydro-1-(1-methyl-2,4-dioxo-1,2,3,4-tetrahydro-5-pyrimidinyl)-d-ribitol
1-methyl-5-beta-d-ribofuranosyluracil
BP-58832
beta-1-methylpseudouridine
EX-A7845K
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
methylpseudouridineA member of the class of pseudouridines that is pseudouridine substituted by a methyl group at unspecified position.
[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 (13)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (23.08)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's6 (46.15)24.3611
2020's4 (30.77)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 43.63

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

MetricThis Compound (vs All)
Research Demand Index43.63 (24.57)
Research Supply Index2.64 (2.92)
Research Growth Index5.33 (4.65)
Search Engine Demand Index59.45 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (43.63)

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%
Other13 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]