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PMID: 11229777 Published · ppublish English Journal Article

Pyrrolidine inhibitors of human cytosolic phospholipase A2. Part 2: synthesis of potent and crystallized 4-triphenylmethylthio derivative 'pyrrophenone'.

Bioorganic & medicinal chemistry letters ·Vol. 11 ·No. 4 ·2001-02-26 ·Pages 587-90

Seno K, Okuno T, Nishi K, Murakami Y, Yamada K, Nakamoto S, Ono T

Abstract

We synthesized a potent and crystallized human cytosolic phospholipase A2alpha inhibitor, pyrrophenone (6) which inhibits the isolated enzyme with an IC50 value of 4.2 nM. Pyrrophenone shows potent inhibition of arachidonic acid release, prostaglandin E2, thromboxane B2, and leukotriene B4 formation in human whole blood. The magnitudes of prostaglandin E2 and thromboxane B2 inhibition are the same as those of indomethacin.

MeSH Terms
Arachidonic Acid/metabolism Crystallization Cytosol/enzymology Dinoprostone/biosynthesis Enzyme Inhibitors/chemical synthesis,pharmacology Humans Phospholipases A/antagonists & inhibitors Phospholipases A2 Pyrrolidines/chemical synthesis,pharmacology Thromboxane B2/biosynthesis
Chemicals
Enzyme Inhibitors Pyrrolidines Arachidonic Acid Thromboxane B2 Phospholipases A Phospholipases A2 Dinoprostone
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Seno K
Shionogi Research Laboratories, Shionogi & Co., Ltd., Osaka, Japan. kaoru.seno@shionogi.co.jp
Okuno T
Nishi K
Murakami Y
Yamada K
Nakamoto S
Ono T
Article Info
Journal
Bioorganic & medicinal chemistry letters
Abbr.
Bioorg Med Chem Lett
ISSN
0960-894X
Published
2001-02-26
Pages
587-90
Language
English
Region
England
NLM ID
9107377
Subset
IM
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