Design, synthesis, and evaluation of a novel series of α-subsituted phenylpropanoic acid derivatives as human peroxisome proliferators-activated receptor (PPAR) α/δ dual agonists for the treatment of metabolic syndrome.
Design, synthesis, and evaluation of a novel series of α-subsituted phenylpropanoic acid derivatives as human peroxisome proliferators-activated receptor (PPAR) α/δ dual agonists for the treatment of metabolic syndrome.
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设计、合成和评估一系列新型 α-取代苯丙酸衍生物,作为人过氧化物酶体增殖物激活受体 (PPAR) α/δ 双激动剂,用于治疗代谢综合征。
DOI:
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发表时间:
2006
期刊:
影响因子:
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通讯作者:
他7名
中科院分区:
文献类型:
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作者:
Jun-ichi Kasuga;他7名
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影响因子:
2.7
作者:
Jun-ichi Kasuga;M. Makishima;Y. Hashimoto;H. Miyachi
通讯作者:
Jun-ichi Kasuga;M. Makishima;Y. Hashimoto;H. Miyachi
影响因子:
2.7
作者:
H. Miyachi;M. Nomura;T. Tanase;Masahiro Suzuki;K. Murakami;K. Awano
通讯作者:
K. Awano
影响因子:
15.9
作者:
Okuno, A;Tamemoto, H;Kadowaki, T
通讯作者:
Kadowaki, T
影响因子:
10.5
作者:
Lim, H;Gupta, RA;Dey, SK
通讯作者:
Dey, SK
DOI:
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发表时间:
2003
期刊:
影响因子:
--
作者:
M. Nomura;T. Tanase;T. Ide;M. Tsunoda;Masahiro Suzuki;H. Uchiki;and Koji Murakami;H. Miyachi
通讯作者:
H. Miyachi