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Development of Drug-Like-Templates : Structure-activity Relationship Study of Tachykinin Peptides for Development of Novel Neurokinin-3 Receptor Selective Agonists

机译：药物样模板的开发：速激肽肽与新型神经激肽3受体选择性激动剂的结构-活性关系研究

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平成24年度京都大学化学研究所スーパーコンピュータシステム利用報告書

机译：2012京都大学化学研究所超级计算机系统使用报告

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大野浩章;
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年度 2013
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1. Structure-activity relationship study of tachykinin peptides for the development of novel neurokinin-3 receptor selective agonists [J] . MisuR., NoguchiT., OhnoH., Bioorganic and medicinal chemistry . 2013,第8期

机译：速激肽开发新型神经激肽3受体选择性激动剂的构效关系研究
2. Structure-activity relationship study on senktide for development of novel potent neurokinin-3 receptor selective agonists [J] . Misu Ryosuke, Yamamoto Koki, Yamada Ai, MedChemComm . 2015,第3期

机译：senktide用于开发新型强效神经激肽3受体选择性激动剂的构效关系研究
3. Erratum: Structure-activity relationship study of N ~6-(2-(4-(1 H -Indol-5-yl)piperazin-1-yl)ethyl)-N ~6-propyl-4,5,6,7- tetrahydrobenzo[d]thiazole-2,6-diamine Analogues: Development of highly selective D3 dopamine receptor agonists along with a highly potent D2/D3 agonist and their pharmacological characterization(Journal of Medicinal Chemistry (2012) 55 (5826-5840)) (Erratum) [J] . Johnson M., Antonio T., Reith M.E.A., Journal of Medicinal Chemistry . 2013,第2期

机译：勘误：N〜6-（2-（4-（1 H-吲哚-5-基）哌嗪-1-基）乙基）-N〜6-丙基-4,5,6,7的构效关系研究-四氢苯并[d]噻唑-2,6-二胺类似物：高选择性D3多巴胺受体激动剂以及高效D2 / D3激动剂的开发及其药理特性（药物化学杂志（2012）55（5826-5840））（勘误表）
4. Structure-Activity Relationship Study of Tachykinin Peptides for the Development of Novel NK3 Receptor Agonists [C] . Ryosuke Misu, Taro Noguchi, Hiroaki Ohno American Peptide Symposium . 2013

机译：特异林蛋白肽在新型NK3受体激动剂发育的结构 - 活性关系研究
5. Selective GLP-1 receptor antagonists and glucagon/GLP-1 co-agonists discovered through an investigation into the structure-activity relationship in glucagon-related peptides. [D] . Patterson, James T. 2011

机译：通过研究胰高血糖素相关肽的结构-活性关系，发现了选择性的GLP-1受体拮抗剂和胰高血糖素/ GLP-1共激动剂。
6. Structure-Activity Relationships of Peptides Incorporating a Bioactive Reverse-Turn Heterocycle at the Melanocortin Receptors: Identification of a 5800-fold Mouse Melanocortin-3 Receptor (mMC3R) Selective Antagonist/Partial Agonist versus the Mouse Melanocortin-4 Receptor (mMC4R) [O] . Anamika Singh, Marvin Dirain, Rachel Witek, -1

机译：在Melanocortin受体上掺入生物逆向杂环的肽的结构-活性关系：鉴定为5800倍小鼠Melanocortin-3受体（mMC3R）选择性拮抗剂/部分激动剂与小鼠Melanocortin-4受体（mMC4R）
7. Structure-activity relationship study of tachykinin peptides for the development of novel neurokinin-3 receptor selective agonists. [O] . Misu Ryosuke, Noguchi Taro, Ohno Hiroaki, 2013

机译：速激肽对新型神经激肽3受体选择性激动剂发展的构效关系研究。

Development of Drug-Like-Templates : Structure-activity Relationship Study of Tachykinin Peptides for Development of Novel Neurokinin-3 Receptor Selective Agonists

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