[Looking Back on My Life in Research over more than 40 Years].

IF 0.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan Pub Date : 2024-01-01 DOI:10.1248/yakushi.23-00153
Takahide Nishi
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Abstract

After graduating with a master's degree from Faculty of Pharmaceutical Sciences, Hokkaido University in 1983, I worked in medicinal chemistry for 37 years at a pharmaceutical company and 4 years at a university. On this occasion of my retirement, I would like to summarize the memorable reactions from my life in research over more than 40 years. This includes an overview of my drug discovery research at pharmaceutical companies covering practical and effective synthetic methods of key intermediates for renin inhibitors, 1β-methylcarbapenem, neurokinin receptor antagonists and sphingosine-1-phosphate receptor agonists. I have also described microbial transformation reactions for phosphorylation and glucuronidation, as well as antibacterial cyclic peptide and ogipeptins. During this time, two years of studying at the Scripps Research Institute and three years of working in India were also very valuable experiences. Finally, I have summarized the results of synthetic research on indole and azaindole derivatives conducted at the Health Sciences University of Hokkaido over a period of four years.

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[回顾我 40 多年的科研生活]。
1983 年从北海道大学药学部硕士毕业后,我在一家制药公司从事了 37 年的药物化学研究,并在一所大学工作了 4 年。值此退休之际,我想总结一下自己 40 多年研究生活中值得纪念的点点滴滴。其中包括我在制药公司的药物发现研究概况,包括肾素抑制剂、1β-甲基碳青霉烯、神经激肽受体拮抗剂和 1-磷酸鞘氨醇受体激动剂的关键中间体的实用有效合成方法。我还描述了磷酸化和葡萄糖醛酸化的微生物转化反应,以及抗菌环肽和寡肽。在此期间,在斯克里普斯研究所学习的两年和在印度工作的三年也是非常宝贵的经历。最后,我总结了四年来在北海道保健科学大学进行的吲哚和氮杂吲哚衍生物合成研究的成果。
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CiteScore
0.60
自引率
0.00%
发文量
169
审稿时长
1 months
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