Compounds > 1-methoxynaphthalene
Page last updated: 2024-09-22

1-methoxynaphthalene

Description

1-methoxynaphthalene: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

methoxynaphthalene : Any alkyloxynaphthalene bearing one or more methoxy substituents. [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 CID16668
SCHEMBL ID151449
SCHEMBL ID3504381
SCHEMBL ID10251245
MeSH IDM0416809

Synonyms (48)

Synonym
naphthalene, 1-methoxy-
methyl 1-naphthyl ether
2216-69-5
.alpha.-methoxynaphthalene
1-methoxynaphthalene
nsc-5530
nsc5530
.alpha.-naphthyl methyl ether
alpha-methoxynaphthalene
nsc 5530
alpha-naphthyl methyl ether
ai3-02144
einecs 218-696-1
1-methoxynapthalene
inchi=1/c11h10o/c1-12-11-8-4-6-9-5-2-3-7-10(9)11/h2-8h,1h
1-methoxynaphthalene, >=98%
M0116
AKOS003632549
1-methoxy-naphthalene
1-methoxy naphthalene
unii-dg2eol57lf
dg2eol57lf ,
A815983
FT-0608014
methoxynaphthalene
SCHEMBL151449
SCHEMBL3504381
1-naphthyl methyl ether
methoxynaphthalene, 1-
1-naphthol methyl ether
SCHEMBL10251245
57982-68-0
DTXSID5062263
Q-200124
AC-23677
mfcd00003924
naphthalene, methoxy-
1-methoxynaphthalene, analytical standard
CS-W013284
DS-3387
BCP30167
1-naphthol methyl ether;naphthalene, 1-methoxy-
O10418
Q27276378
?1-methoxynaphthalene
HY-W012568
EN300-16125
PD158288

Research

Studies (12)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (8.33)18.7374
1990's1 (8.33)18.2507
2000's2 (16.67)29.6817
2010's8 (66.67)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

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%
Other12 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceDescriptionRelationhip StrengthStudiesTrialsClassesRoles
guaiacol[no description available]medium10guaiacolsdisinfectant;
EC 1.1.1.25 (shikimate dehydrogenase) inhibitor;
expectorant;
plant metabolite
heme[no description available]medium10
1-benzylpiperazine[no description available]medium10N-alkylpiperazineenvironmental contaminant;
psychotropic drug;
serotonergic agonist;
xenobiotic
1-hexanol[no description available]medium10hexanol;
primary alcohol		alarm pheromone;
antibacterial agent;
fragrance;
plant metabolite
silver[no description available]medium10copper group element atom;
elemental silver		Escherichia coli metabolite
phenyl acetate[no description available]medium10benzenes;
phenyl acetates
palmitic acid[no description available]medium10long-chain fatty acid;
straight-chain saturated fatty acid		algal metabolite;
Daphnia magna metabolite;
EC 1.1.1.189 (prostaglandin-E2 9-reductase) inhibitor;
plant metabolite
hydrogen[no description available]medium10elemental hydrogen;
elemental molecule;
gas molecular entity		antioxidant;
electron donor;
food packaging gas;
fuel;
human metabolite
styrene[no description available]medium10styrenes;
vinylarene;
volatile organic compound		mouse metabolite;
mutagen;
plant metabolite
2-methylnaphthalene[no description available]medium10methylnaphthalene
naphthyl sulfate[no description available]medium10
1-naphthol[no description available]medium10naphtholgenotoxin;
human xenobiotic metabolite
1,4-naphthoquinone[no description available]medium101,4-naphthoquinones
naphthoquinones[no description available]medium10
2-naphthol[no description available]medium10naphtholantinematodal drug;
genotoxin;
human urinary metabolite;
human xenobiotic metabolite;
mouse metabolite;
radical scavenger
phenanthrenes[no description available]medium10
ConditionIndicatedRelationship StrengthStudiesTrials

Research Highlights

Safety/Toxicity (1)

ArticleYear
Synthesis, antidepressant activity, and toxicity of the erythro/threo racemates and optical isomers of 2-(4-benzylpiperazin-1-yl)-1-(5-chloro-6-methoxynaphthalen-2-yl)hexan-1-ol.
Chemical biology & drug design, Volume: 85, Issue: 4		2015
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]