Page last updated: 2024-12-08

5-o-methyl-myo-inositol

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

Description

1D-5-O-methyl-myo-inositol : A member of the class of methyl myo-inositols that is cyclohexane-1,2,3,4,5-pentol substituted by a methoxy group at position 6 (the 1R,2S,3r,4R,5S,6r-stereoisomer). [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 CID439990
CHEMBL ID460057
CHEBI ID179104
CHEBI ID15975
SCHEMBL ID1888646
SCHEMBL ID7155914
SCHEMBL ID1059036
MeSH IDM0574056

Synonyms (36)

Synonym
(1s,2r,4s,5r)-6-methoxycyclohexane-1,2,3,4,5-pentol
CHEBI:179104
(1r,2s,3r,4r,5s,6r)-6-methoxycyclohexane-1,2,3,4,5-pentol
CHEBI:15975
o-methyl-scyllo-inositol
C03365
523-92-2
1d-5-o-methyl-myo-inositol
C05163
sequoyitol
1-o-methyl-scyllo-inositol
5-o-methyl-myo-inositol ,
6A797581-AC95-4A84-9F74-C05E5465011A
BMSE000740
(1r,2s,4r,5s)-6-methoxycyclohexane-1,2,3,4,5-pentol
CHEMBL460057
AKOS006272498
SCHEMBL1888646
SCHEMBL7155914
S9343
myo-inositol, 5-o-methyl-
einecs 208-352-9
SCHEMBL1059036
AC-32615
2-o-methyl-myo-inositol
(1r,2s,3r,4r,5s,6r)-6-methoxycyclohexane-1,2,3,4,5-pentaol
(+)-3-o-methyl-d-chiro-inositol
HY-N2421
Q27098326
CCG-266528
CS-0022628
MS-23046
(1r,2s,4r,5s)-6-methoxycyclohexane-1,2,3,4,5-pentaol
DTXSID801313753
7600-53-5
E80607
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
cyclohexanolsAn alcohol in which one or more hydroxy groups are attached to a cyclohexane skeleton.
[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 (1)

PathwayProteinsCompounds
pinitol biosynthesis II016

Bioassays (1)

Assay IDTitleYearJournalArticle
AID361505Effect on amyloid beta 42 aggregation assessed as inhibition of fiber formation at 5 mM2008Bioorganic & medicinal chemistry, Aug-01, Volume: 16, Issue:15
Synthesis of scyllo-inositol derivatives and their effects on amyloid beta peptide aggregation.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (9)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (11.11)18.7374
1990's0 (0.00)18.2507
2000's1 (11.11)29.6817
2010's7 (77.78)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: 13.06

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 Index13.06 (24.57)
Research Supply Index2.30 (2.92)
Research Growth Index5.37 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (13.06)

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%
Other9 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]