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Titlebook: Hypotensive Peptides; Proceedings of the I Ervin G. Erdös (Professor of Pharmacology),Nathan Conference proceedings 1966 Springer-Verlag N

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书目名称Hypotensive Peptides
副标题Proceedings of the I
编辑Ervin G. Erdös (Professor of Pharmacology),Nathan
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图书封面Titlebook: Hypotensive Peptides; Proceedings of the I Ervin G. Erdös (Professor of Pharmacology),Nathan  Conference proceedings 1966 Springer-Verlag N
描述The papers collected in this volume were presented at the International Symposium on Hypotensive Peptides held in Flor­ ence, Italy, on October 25-29, 1965. The purpose of the meeting was to bring together scientists of fourteen countries ranging from the chemist to the surgeon, who usually do not speak a common language and for whom it would be quite difficult to follow the latest developments in fields allied to, but still some­ what removed from their basic interest. Their reports sum­ marized their recent progress and current achievements, and gave indication of the trend that future research on hypotensive peptides may take. Various aspects of the structure and function of brady­ kinin, kallidin, kallikrein, gastrin, eledoiSin, physalaemin, sub­ stance P, and related substances were discussed during the nine sessions. The first session was devoted to the chemistry of peptides. This was followed in loose order by reports dealing with the structure of some newer peptides, with kininogen, and with enzymes that release or inactivate peptides. Subsequently, reports on the physiological, pharmacological, pathological, and clinical importance of kinins, kallikrein, and eledoisin were
出版日期Conference proceedings 1966
关键词Isomer; Lipid; amino acid; chemistry; circulation; development; enzyme; enzymes; fields; nomenclature; paper; p
版次1
doihttps://doi.org/10.1007/978-3-642-94965-4
isbn_softcover978-3-642-94967-8
isbn_ebook978-3-642-94965-4
copyrightSpringer-Verlag New York Inc. 1966
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Constructing effective paragraphsDuring the past year, a considerable amount of preliminary work has been carried out by Dr. P. S. Venkateswaran in my laboratory toward the synthesis of modified peptides with longer duration of action. I take this opportunity to present for the first time our basic approach to this problem.
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https://doi.org/10.1057/9780333992746In order to find out how kinin is bound in the kininogen molecule, pure kininogen should be hydrolyzed by kininogenases and the free end-groups of the resulting products determined.
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https://doi.org/10.1057/9780230601796During the 1962 Symposium in New York, I reported the isolation and described some of the properties of beef serum kininogen and hog pancreatic kallikreins, components of the last step of kinin formation (Habermann, 1963). Since that time my efforts have been directed toward abetter understanding of this part of the kinin system.
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What Is Health Insurance (Good) For?Enzymes of diverse origin form kinin when incubated with plasma globulins. Trypsin has been used as a model for kinin-releasing enzymes since the discovery of bradykinin by Rocha e Silva .. (1949).
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