Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Wan-Ping Hsieh"'
Autor:
Wan-Ping Hsieh, 謝琬萍
89
The first project described in this thesis is the investigation of the rductive alkylation of γ-cyano-α,β-unsaturated enones 58 and 59 by sequential treatment with lithium naphthalenide and an alkylating agent. The reduction precursors 58
The first project described in this thesis is the investigation of the rductive alkylation of γ-cyano-α,β-unsaturated enones 58 and 59 by sequential treatment with lithium naphthalenide and an alkylating agent. The reduction precursors 58
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/56391422721704046774
Autor:
Wen-Chi Hsiao, Yu-Sheng Chao, Kak-Shan Shia, Chia-Yu Hsu, Wan-Ping Hsieh, Yinchiu Lin, Teng-Kuang Yeh, Ming-Shiu Hung, Shi-Liang Tseng
Publikováno v:
Pharmacological Research. 62:337-343
A novel alkynylthiophene series of cannabinoid CB1 receptor antagonists has been described to exhibit distinct intrinsic activities with minimal substructure modifications. The three representatives, BPR0432, BPR0568 and BPR0569, functioning as a neu
Autor:
Chien-Huang Wu, Ming-Shiu Hung, Chin-Yu Lin, Min-Tsang Hsieh, Jiing-Jyh Jan, Cheng-Ming Chu, Kak-Shan Shia, Ming-Chen Chou, Teng-Kuang Yeh, Horng-Shing Shy, Jen-Shin Song, Yu-Sheng Chao, Shi-Liang Tseng, Yen-Nan Yeh, Wan-Ping Hsieh, Yinchiu Lin, Chun-Wei Kuo, Wan-Ling Chung, Chun-Ping Chang
Publikováno v:
Journal of Medicinal Chemistry. 52:4496-4510
By using the active metabolite 5 as an initial template, further structural modifications led to the identification of the titled compound 24 (BPR-890) as a highly potent CB1 inverse agonist possessing an excellent CB2/1 selectivity and remarkable in
Autor:
Hua-Hao Chiu, Jen-Shin Song, Wan-Ping Hsieh, Ming-Shiu Hung, Cheng-Ming Chu, Kak-Shan Shia, Yen-Shih Tung, Chun-Ping Chang, Yu-Sheng Chao, Shi-Liang Tseng, Chien-Huang Wu, Yinchiu Lin, Wan-Ling Chung, Chia-Liang Tai, Chun-Wei Kuo
Publikováno v:
Journal of Medicinal Chemistry. 51:5397-5412
Replacing the conventional pyrazole 5-aryl substituent of 1 (SR141716A) with the 2-thienyl moiety appended with an appropriate alkynyl unit, a novel class of 5-(5-alkynyl-2-thienyl)pyrazole derivatives, behaving as highly potent CB1 receptor antagoni
Autor:
Chao Yu-Sheng, Min-Tsang Hsieh, Chia Chien Hsieh, Kak Shan Shia, Chun Wei Kuo, Hui Chuan Wu, Wan Ping Hsieh, Chia Liang Tai, Ming Shiu Hung, Jing Po Tsao, Jen Shin Song, Shi Liang Tseng, Vijay D. Pawar, Hua Hao Chiu
Publikováno v:
Org. Biomol. Chem.. 6:447-450
A novel class of (5-(pent-1-enyl)thiophen-2-yl)pyrazole antagonists was discovered, many of which exhibited potent CB1 activity and good CB1/2 selectivity, suggesting that along with a 1,3-transposition of the carbonyl of the pyrazole 3-carboxamide,
Autor:
Shi-Liang, Tseng, Ming-Shiu, Hung, Chun-Ping, Chang, Jen-Shin, Song, Chia-Liang, Tai, Hua-Hao, Chiu, Wan-Ping, Hsieh, Yinchiu, Lin, Wan-Ling, Chung, Chun-Wei, Kuo, Chien-Huang, Wu, Cheng-Ming, Chu, Yen-Shih, Tung, Yu-Sheng, Chao, Kak-Shan, Shia
Publikováno v:
Journal of medicinal chemistry. 51(17)
Replacing the conventional pyrazole 5-aryl substituent of 1 (SR141716A) with the 2-thienyl moiety appended with an appropriate alkynyl unit, a novel class of 5-(5-alkynyl-2-thienyl)pyrazole derivatives, behaving as highly potent CB1 receptor antagoni