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PMID: 3420158 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A fluorescent protein kinase C inhibitor: 1-(1-hydroxy-5-isoquinolinylsulfonyl)piperazine.

Pharmacology ·Vol. 36 ·No. 6 ·1988-00-00 ·Pages 365-70

Hagiwara M, Inagaki M, Takahashi J, Yoshida T, Hidaka H

Abstract

The isoquinolinesulfonamide compound 1-(5-isoquinolinyl-sulfonyl)-2-methylpiperazine (H-7) has been widely used as a protein kinase C inhibitor. Although H-7 and its derivatives are useful for the demonstration of the biological function of protein kinase C or cyclic nucleotide-dependent protein kinases, these compounds are not available for a histological approach to protein kinase C. In the present study, we introduce 1-(1-hydroxy-5-isoquinolinylsulfonyl)piperazine (hydroxy H-7) as a useful tool in tissue experiments. The property of the compound as a protein kinase C inhibitor was similar to that of H-7. Hydroxy H-7 inhibited the enzyme in a competitive manner with ATP, the Ki value was 23 microM, and exhibited a fluorescence property with a maximum emission wavelength of 444 nm excited at 350 nm. Fluoromicroscopical investigations revealed that hydroxy H-7 penetrated the cell membrane and was distributed mainly in the cytoplasm.

MeSH Terms
1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine Adenosine Triphosphate/metabolism Animals Cells, Cultured Isoquinolines/pharmacology Macropodidae Piperazines/pharmacology Protein Kinase C/antagonists & inhibitors Spectrometry, Fluorescence Spectrophotometry, Ultraviolet
Chemicals
Isoquinolines Piperazines 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine Adenosine Triphosphate Protein Kinase C
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Hagiwara M
Department of Pharmacology, Nagoya University School of Medicine, Japan.
Inagaki M
Takahashi J
Yoshida T
Hidaka H
Article Info
Journal
Pharmacology
Abbr.
Pharmacology
ISSN
0031-7012
Published
1988-00-00
Pages
365-70
Language
English
Region
Switzerland
NLM ID
0152016
Subset
IM
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