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Structure-activity relationships for...
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Yamamoto, Koki.
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Structure-activity relationships for development of neurokinin-3 receptor antagonists = reducing environmental impact /
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Structure-activity relationships for development of neurokinin-3 receptor antagonists/ by Koki Yamamoto.
其他題名:
reducing environmental impact /
作者:
Yamamoto, Koki.
出版者:
Singapore :Springer Singapore : : 2020.,
面頁冊數:
xii, 86 p. :ill., digital ;24 cm.
內容註:
1. Introduction -- 2. Development of NK3R Antagonists with a Labile Functional Group in the Natural Environment -- 3. Development of NK3R Antagonists with a Degradable Scaffold in the Natural Environment: Synthesis and Application of Fused Piperazine Derivatives for Investigation of Degradable Core Motifs -- 4. Development of NK3R Antagonists with a Degradable Scaffold in the Natural Environment: Identification of NK3R Antagonists with a Decomposable Core Structure by Scaffold Hopping -- 5. Conclusion.
Contained By:
Springer eBooks
標題:
Bioorganic Chemistry. -
電子資源:
https://doi.org/10.1007/978-981-15-2965-8
ISBN:
9789811529658
Structure-activity relationships for development of neurokinin-3 receptor antagonists = reducing environmental impact /
Yamamoto, Koki.
Structure-activity relationships for development of neurokinin-3 receptor antagonists
reducing environmental impact /[electronic resource] :by Koki Yamamoto. - Singapore :Springer Singapore :2020. - xii, 86 p. :ill., digital ;24 cm. - Springer theses,2190-5053. - Springer theses..
1. Introduction -- 2. Development of NK3R Antagonists with a Labile Functional Group in the Natural Environment -- 3. Development of NK3R Antagonists with a Degradable Scaffold in the Natural Environment: Synthesis and Application of Fused Piperazine Derivatives for Investigation of Degradable Core Motifs -- 4. Development of NK3R Antagonists with a Degradable Scaffold in the Natural Environment: Identification of NK3R Antagonists with a Decomposable Core Structure by Scaffold Hopping -- 5. Conclusion.
This book explores the possible development of neurokinin-3 receptor (NK3R) antagonists with reduced environmental impact. Pharmaceuticals are used to cure diseases and to alleviate symptoms in humans and animals. However, the stable, bioactive substances excreted by patients have unfavorable effects on non-target species. To overcome these disadvantages of these highly stable, potent substances, drug design to turn off bioactivity after release into the environment is needed. The book describes the development of eco-friendly NK3R antagonists by introducing a labile functional moiety and substituting a scaffold. This resulted in a novel NK3R antagonist that oxidized into its inactive form when exposed to air. Further, the book presents an efficient and easily achievable synthetic method of creating triazolopiperazine scaffolds, as well as a structure-activity relationship study involving scaffold hopping for decomposable motifs, which led to a novel photodegradable NK3R antagonist. Demonstrating that it is possible to develop compounds that convert into their inactive forms under environmental conditions, this book is useful for anyone interested in therapeutic agents with reduced environmental impact.
ISBN: 9789811529658
Standard No.: 10.1007/978-981-15-2965-8doiSubjects--Topical Terms:
899222
Bioorganic Chemistry.
LC Class. No.: RM301.42 / .Y363 2020
Dewey Class. No.: 615.19
Structure-activity relationships for development of neurokinin-3 receptor antagonists = reducing environmental impact /
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This book explores the possible development of neurokinin-3 receptor (NK3R) antagonists with reduced environmental impact. Pharmaceuticals are used to cure diseases and to alleviate symptoms in humans and animals. However, the stable, bioactive substances excreted by patients have unfavorable effects on non-target species. To overcome these disadvantages of these highly stable, potent substances, drug design to turn off bioactivity after release into the environment is needed. The book describes the development of eco-friendly NK3R antagonists by introducing a labile functional moiety and substituting a scaffold. This resulted in a novel NK3R antagonist that oxidized into its inactive form when exposed to air. Further, the book presents an efficient and easily achievable synthetic method of creating triazolopiperazine scaffolds, as well as a structure-activity relationship study involving scaffold hopping for decomposable motifs, which led to a novel photodegradable NK3R antagonist. Demonstrating that it is possible to develop compounds that convert into their inactive forms under environmental conditions, this book is useful for anyone interested in therapeutic agents with reduced environmental impact.
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