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【下載完整報告】AI熱潮從學術研究也能看出端倪?哪些議題是2023熱搜議題?
期刊
Structural Development Studies of Subtype-Selective Ligands for Peroxisome Proliferator-Activated Receptors (PPARs) Based on the 3,4-Disubstituted Phenylpropanoic Acid Scaffold as a Versatile Template
Hiroyuki Miyachi
;
Yuichi Hashimoto
《PPAR Research》
2008卷
(2008/12)
Pp. 937-951-091
https://doi.org/10.1155/2008/689859
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延伸閱讀
楊承翰(2015)。
Self-assembly, Structures, and Properties of Metal—Organic Compounds with Pyrimidine and Imidazole Ligands
〔碩士論文,國立中正大學〕。華藝線上圖書館。https://www.airitilibrary.com/Article/Detail?DocID=U0033-2110201614030150
Agarwal, N., Bajpai, A., & Gupta, S. P. (2013).
A Quantitative Structure-Activity Relationship and Molecular Modeling Study on a Series of Heteroaryl- and Heterocyclyl-Substituted Imidazo[1,2-a]Pyridine Derivatives Acting as Acid Pump Antagonists
.
Biochemistry Research International
,
2013
(), 4-18. https://doi.org/10.1155/2013/141469
Li, C. Y. (2022).
Structural and functional elucidation of adenylation domain of nonribosomal peptide synthetase-like protein in Aspulvinone E biosynthesis
[master's thesis, National Taiwan University]. Airiti Library. https://doi.org/10.6342/NTU202202724
吳慧娟 (2014).
Synthesis and Structure-activity Relationship Study of Novel 1,5-Diarylpyrrole as Potent and Selective CB1 Cannabinoid Receptor Ligands
[doctoral dissertation, National Tsing Hua University]. Airiti Library. https://www.airitilibrary.com/Article/Detail?DocID=U0016-2912201413514161
Chen, C. S., Lai, S. Y., Hsu, P. S., Tsai, C. Y., Fang, C. W., Su, M. J., Cheng, F. C., Kao, C. L., & Chem, J. W. (2002).
Design, Synthesis and Biological Evaluation of Heterocycle-Conjugated Styrene Derivatives as Protein Tyrosine Kinase Inhibitors and Free Radical Scavengers
.
The Chinese Pharmaceutical Journal
,
54
(5), 353-374. https://doi.org/10.7019/CPJ.200210.0353
國際替代計量
Structural Development Studies of Subtype-Selective Ligands for Peroxisome Proliferator-Activated Receptors (PPARs) Based on the 3,4-Disubstituted Phenylpropanoic Acid Scaffold as a Versatile Template
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