Page last updated: 2024-12-06

2-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline

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

Description

2-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline: present in parkinsonian & normal human brains; RN given refers to parent cpd; structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID37764
CHEMBL ID544714
CHEMBL ID1193326
CHEBI ID89546
SCHEMBL ID6247473
MeSH IDM0188941

Synonyms (23)

Synonym
6,7-isoquinolinediol, 1,2,3,4-tetrahydro-2-methyl-
1,2,3,4-tetrahydro-2-methyl-6,7-isoquinolinediol
2-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline
brn 0150401
2-methyl-3,4-dihydro-1h-isoquinoline-6,7-diol
2-methyl-1,2,3,4-tetrahydroisoquinolin-2-ium-6,7-diol chloride
2-methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol
bdbm50014647
chembl544714 ,
1,2-dimethyl-1,2,3,4-tetrahydro-isoquinoline-6,7-diol; hydrobromide
CHEMBL1193326
chebi:89546 ,
37491-98-8
4-21-00-02109 (beilstein handbook reference)
unii-qvw3czk8sf
qvw3czk8sf ,
SCHEMBL6247473
WETXYFNVBDLWIW-UHFFFAOYSA-N
1,2,3,4-tetrahydroisoquinolin-6,7-diol, 2-methyl-
2-methyl-1,2,3,4-tetrahydro-6,7-isoquinolinediol #
2(n)-methyl-norsalsolinol
DTXSID70190942
Q27161747
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
human metaboliteAny mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
rat metaboliteAny mammalian metabolite produced during a metabolic reaction in rat (Rattus norvegicus).
neurotoxinA poison that interferes with the functions of the nervous system.
[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 (2)

ClassDescription
isoquinolinol
tertiary amino compoundA compound formally derived from ammonia by replacing three hydrogen atoms by organyl groups.
[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-19900 (0.00)18.7374
1990's10 (76.92)18.2507
2000's3 (23.08)29.6817
2010's0 (0.00)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: 11.57

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 Index11.57 (24.57)
Research Supply Index2.64 (2.92)
Research Growth Index4.21 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.57)

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]