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Isoquinolines

Known as: 2 benzazine, Isoquinolines [Chemical/Ingredient], isoquinoline 
A group of compounds with the heterocyclic ring structure of benzo(c)pyridine. The ring structure is characteristic of the group of opium alkaloids… 
National Institutes of Health

Related topics

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50 relations

Narrower (49)

1-aminoisoquinoline3-acetylisoquinolineA-317567Almorexant
antagonists & inhibitors

Papers overview

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Highly Cited
2011
Highly Cited
2011
A dual-catalysis approach to the asymmetric Steglich rearrangement and catalytic enantioselective addition of O-acylated azlactones to isoquinolines.
A dual-catalysis approach, namely the combination of an achiral nucleophilic catalyst and a chiral anion-binding catalyst, was… 
Highly Cited
2007
Highly Cited
2007
Synthesis of pyrrolo-isoquinolines related to the lamellarins using silver-catalyzed cycloisomerization/dipolar cycloaddition.
Synthesis of pyrrolo-isoquinolines related to the lamellarin alkaloids employing silver-catalyzed cycloisomerization−dipolar… 
Highly Cited
2007
Highly Cited
2007
Poppy alkaloid profiling by electrospray tandem mass spectrometry and electrospray FT-ICR mass spectrometry after [ring-13C6]-tyramine feeding.
Review
2002
Review
2002
Dopamine-derived endogenous N-methyl-(R)-salsolinol: its role in Parkinson's disease.
Highly Cited
1997
Highly Cited
1997
Free radical scavengers protect dopaminergic cell lines from apoptosis induced by complex I inhibitors.
Highly Cited
1996
Highly Cited
1996
Dopamine-derived endogenous 1(R),2(N)-dimethyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline, N-methyl-(R)-salsolinol, induced parkinsonism in rat: biochemical, pathological and behavioral studies
Review
1995
Review
1995
A matter of some sensitivity.
Highly Cited
1983
Highly Cited
1983
The anxiogenic action of Ro 5-4864 is reversed by phenytoin
Highly Cited
1982
Highly Cited
1982
HL 725, an extremely potent inhibitor of platelet phosphodiesterase and induced platelet aggregation in vitro.
Highly Cited
1978
Highly Cited
1978
Tetrahydroisoquinolines derived from catecholamines or DOPA: effects on brain tyrosine hydroxylase activity.
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