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coerulescine

Description

coerulescine: structure in first source [MeSH]

Cross-References

ID SourceID
PubMed CID12297097
MeSH IDM0458429

Synonyms (2)

Synonym
coerulescine
(3r)-1'-methylspiro[1h-indole-3,3'-pyrrolidine]-2-one

Research

Studies (10)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (20.00)29.6817
2010's7 (70.00)24.3611
2020's1 (10.00)2.80

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%
Other10 (100.00%)84.16%
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
acetaldehydealdehydecarcinogenic agent;
EC 3.5.1.4 (amidase) inhibitor;
electron acceptor;
Escherichia coli metabolite;
human metabolite;
mouse metabolite;
mutagen;
oxidising agent;
Saccharomyces cerevisiae metabolite;
teratogenic agent
2014201410.0low000010
methanealkane;
gas molecular entity;
mononuclear parent hydride;
one-carbon compound
bacterial metabolite;
fossil fuel;
greenhouse gas
2014201410.0low000010
itaconic aciddicarboxylic acid;
dicarboxylic fatty acid;
olefinic compound
fungal metabolite;
human metabolite
2003200321.0low000100
physostigminecarbamate ester;
indole alkaloid
antidote to curare poisoning;
EC 3.1.1.8 (cholinesterase) inhibitor;
miotic
201520168.5low000020
nitromethaneprimary nitroalkane;
volatile organic compound
EC 4.3.1.3 (histidine ammonia-lyase) inhibitor;
explosive;
NMR chemical shift reference compound;
polar aprotic solvent
2014201410.0low000010
4-anisidinemethoxybenzenes;
primary amino compound;
substituted aniline
genotoxin;
reagent
2003200321.0low000100
3-hydroxybutanal201520159.0low000010
pyrrolespyrrole;
secondary amine
2013201311.0low000010
piperidineazacycloalkane;
piperidines;
saturated organic heteromonocyclic parent;
secondary amine
base;
catalyst;
human metabolite;
non-polar solvent;
plant metabolite;
protic solvent;
reagent
2012201212.0low000010
3-iodoaniline2003200321.0medium000100
pyrrolidineazacycloalkane;
pyrrolidines;
saturated organic heteromonocyclic parent
2012201212.0low000010
alkenes2003200321.0low000100
tryptolinebeta-carbolines2009200915.0low000100
dimethyldioxirane2009200915.0low000100
2-oxindolegamma-lactam;
indolinone
2012201511.0medium000030
esermethole201520159.0medium000010
physovenineindoles201520168.5high000020
martinelline2013201311.0medium000010
horsfiline2003201513.0high000240
piperidines2012201212.0low000010
ConditionIndicatedStudiesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020