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isoquinoline 1-oxidoreductase

Known as: isoquinoline 1-hydroxylase 
National Institutes of Health

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Broader (1)

Oxidoreductases Acting on CH-CH Group Donors

Papers overview

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2019
2019
Molecular Docking Study, Cytotoxicity, Cell Cycle Arrest and Apoptotic Induction of Novel Chalcones Incorporating Thiadiazolyl Isoquinoline in Cervical Cancer.
BACKGROUND Chalcones are naturally occurring compounds found in various plant species which are widely used for traditional… 
2011
2011
Synthesis, structure-activity relationship and in vitro biological evaluation of N-arylethyl isoquinoline derivatives as Coxsackievirus B3 inhibitors.
2008
2008
Behavioral effects of dietary cholesterol in rats tested in experimental models of mild stress and cognition tasks
Review
2006
Review
2006
Development of ligands for the peripheral benzodiazepine receptor.
The peripheral benzodiazepine receptor (PBR) initially characterised as a high affinity binding site for diazepam, is densely… 
1997
1997
Comparative EPR and redox studies of three prokaryotic enzymes of the xanthine oxidase family: quinoline 2-oxidoreductase, quinaldine 4-oxidase, and isoquinoline 1-oxidoreductase.
For three prokaryotic enzymes of the xanthine oxidase family, namely quinoline 2-oxidoreductase, quinaldine 4-oxidase, and… 
1994
1994
Purification and characterization of isoquinoline 1-oxidoreductase from Pseudomonas diminuta 7, a novel molybdenum-containing hydroxylase.
Highly Cited
1989
Highly Cited
1989
Protein kinase inhibitor prevents pulmonary edema in response to H2O2.
We investigated the effect of H2O2 (92 microM) in isolated guinea pig lungs perfused with a buffered Ringer solution. Pulmonary… 
Highly Cited
1989
Highly Cited
1989
Comparative studies of the inhibitory properties of antibiotics on human immunodeficiency virus and avian myeloblastosis virus reverse transcriptases and cellular DNA polymerases.
The inhibition of human immunodeficiency virus (HIV) reverse transcriptase by certain antibiotics and related compounds was… 
1988
1988
Effects of N-hydroxy-N'-aminoguanidine isoquinoline in combination with other inhibitors of ribonucleotide reductase on L1210 cells.
The 1-isoquinolylmethylene derivative of N-hydroxy-N'-aminoguanidine (HAG) is the most potent agent of the recently synthesized… 
1977
1977
INACTIVATION AND INHIBITION OF ROUS SARCOMA VIRUS BY COPPER‐BINDING LIGANDS: THIOSEMICARBAZONES, 8‐HYDROXYQUINOLINES, AND ISONICOTINIC ACID HYDRAZIDE *
We have shown that three types of copper-binding ligands, thiosemicarbazones, 8-hydroxyquinolines, and isonicotinic acid… 
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