Page last updated: 2024-11-07

5'-deoxy-5'-s-isobutylthioadenosine

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

Description

5'-deoxy-5'-S-isobutylthioadenosine: considered an analog of S-adenosylhomocysteine; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID123674
CHEMBL ID427359
SCHEMBL ID2116144
MeSH IDM0062062

Synonyms (25)

Synonym
PDSP2_001019
siba
PDSP1_001035
5'-s-isobutyl-5'-deoxyadenosine
5'-deoxy-5'-s-isobutylthioadenosine
5'-deoxy-5'-s-isobutyladenosine
5'-s-isobutylthioadenosine
adenosine, 5'-s-(2-methylpropyl)-5'-thio-
35899-54-8
(2r,3r,4s,5s)-2-(6-aminopurin-9-yl)-5-(2-methylpropylsulfanylmethyl)oxolane-3,4-diol
CHEMBL427359
SCHEMBL2116144
cas_35899-54-8
bdbm82524
5'-deoxy-5'-isobutylthioadenosine
5'-isobutylthio-5'-deoxyadenosine
S2971
CS-5062
HY-18684
AKOS030526790
BS-16619
(2r,3r,4s,5s)-2-(6-amino-9h-purin-9-yl)-5-((isobutylthio)methyl)tetrahydrofuran-3,4-diol
D71046
9-[5-s-(2-methylpropyl)-5-thiopentofuranosyl]-9h-purin-6-amine
DTXSID10957314
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (1)

Other Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
S-methyl-5'-thioadenosine phosphorylaseHomo sapiens (human)Km3.10003.10004.67506.0000AID239753
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (6)

Processvia Protein(s)Taxonomy
nicotinamide riboside catabolic processS-methyl-5'-thioadenosine phosphorylaseHomo sapiens (human)
nucleobase-containing compound metabolic processS-methyl-5'-thioadenosine phosphorylaseHomo sapiens (human)
purine ribonucleoside salvageS-methyl-5'-thioadenosine phosphorylaseHomo sapiens (human)
L-methionine salvage from methylthioadenosineS-methyl-5'-thioadenosine phosphorylaseHomo sapiens (human)
methylationS-methyl-5'-thioadenosine phosphorylaseHomo sapiens (human)
response to testosteroneS-methyl-5'-thioadenosine phosphorylaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (3)

Processvia Protein(s)Taxonomy
1,4-alpha-oligoglucan phosphorylase activityS-methyl-5'-thioadenosine phosphorylaseHomo sapiens (human)
protein bindingS-methyl-5'-thioadenosine phosphorylaseHomo sapiens (human)
S-methyl-5-thioadenosine phosphorylase activityS-methyl-5'-thioadenosine phosphorylaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (3)

Processvia Protein(s)Taxonomy
nucleoplasmS-methyl-5'-thioadenosine phosphorylaseHomo sapiens (human)
cytosolS-methyl-5'-thioadenosine phosphorylaseHomo sapiens (human)
extracellular exosomeS-methyl-5'-thioadenosine phosphorylaseHomo sapiens (human)
cytosolS-methyl-5'-thioadenosine phosphorylaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (5)

Assay IDTitleYearJournalArticle
AID239753Km against human methylthioadenosine phosphorylase expressed in Escherichia coli BL21 DE3 cells2005Bioorganic & medicinal chemistry letters, Jun-02, Volume: 15, Issue:11
Design, synthesis, and biological evaluation of novel human 5'-deoxy-5'-methylthioadenosine phosphorylase (MTAP) substrates.
AID1589304Inhibition of purified rat liver 5'-nucleotidase using IMP as substrate assessed as reduction in substrate dephosphorylation at 2 to 6 mM2019European journal of medicinal chemistry, Apr-15, Volume: 168Lead optimization and biological evaluation of fragment-based cN-II inhibitors.
AID662565Growth inhibition of Trichomonas vaginalis T1 at 100 uM after 24 hrs by hemocytometry2012Bioorganic & medicinal chemistry letters, Jun-15, Volume: 22, Issue:12
S-Adenosylhomocysteine hydrolase of the protozoan parasite Trichomonas vaginalis: potent inhibitory activity of 9-(2-deoxy-2-fluoro-β,D-arabinofuranosyl)adenine.
AID242855Kcat against human methylthioadenosine phosphorylase expressed in Escherichia coli BL21 DE3 cells2005Bioorganic & medicinal chemistry letters, Jun-02, Volume: 15, Issue:11
Design, synthesis, and biological evaluation of novel human 5'-deoxy-5'-methylthioadenosine phosphorylase (MTAP) substrates.
AID243020Ratio of Kcat to Km against human Methylthioadenosine phosphorylase2005Bioorganic & medicinal chemistry letters, Jun-02, Volume: 15, Issue:11
Design, synthesis, and biological evaluation of novel human 5'-deoxy-5'-methylthioadenosine phosphorylase (MTAP) substrates.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (42)

TimeframeStudies, This Drug (%)All Drugs %
pre-199033 (78.57)18.7374
1990's4 (9.52)18.2507
2000's3 (7.14)29.6817
2010's2 (4.76)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 10.38

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 Index10.38 (24.57)
Research Supply Index3.81 (2.92)
Research Growth Index4.18 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (10.38)

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%
Other44 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]