Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Kai, Zhenpeng"'
Autor:
Yang, Yang, Wu, Yichu, Zhang, Ruimeng, Jin, Meichen, Chen, Zijian, Li, Chunyu, Xu, Shibo, Song, Lixing, Kai, Zhenpeng, Wang, Zhonghua, Wu, Fanhong
Publikováno v:
In Tetrahedron 10 September 2024 164
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
So, Wai Lok1,2 (AUTHOR) henrysowailok@yahoo.com.hk, Kai, Zhenpeng3 (AUTHOR) kaizp@sit.edu.cn, Qu, Zhe1,2 (AUTHOR) quzheouc@gmail.com, Bendena, William G.4 (AUTHOR) bendenaw@queensu.ca, Hui, Jerome H. L.1,2 (AUTHOR) bendenaw@queensu.ca
Publikováno v:
International Journal of Molecular Sciences. Jun2022, Vol. 23 Issue 11, p5998-5998. 11p.
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 29:890-895
Allatostatins (AST) are neuropeptides originally described as inhibitors of juvenile hormone (JH) synthesis in insects. Consequently, they have been considered as potential lead compounds for the discovery of new insect growth regulators (IGRs). In t
Autor:
Li, Xinghai, Yang, Xinling, Liang, Xiaomei, Kai, Zhenpeng, Yuan, Huizu, Yuan, Dekai, Zhang, Jianjun, Wang, Ruiqing, Ran, Fuxiang, Qi, Shuhua, Ling, Yun, Chen, Fuheng, Wang, Daoquan
Publikováno v:
In Bioorganic & Medicinal Chemistry 2008 16(8):4538-4544
Autor:
Hong-ling Zhang, Kai Zhenpeng, Han Yang, Ren Yujie, Shan-shan Chen, Hui-juan Yang, Shan-shan Huang
Publikováno v:
Journal of Agricultural and Food Chemistry. 66:3644-3650
FGLamide allatostatins (ASTs) are regarded as possible insecticide candidates, although their lack of in vivo effects, rapid degradation, poor water solubility, and high production costs preclude their practical use in pest control. In contrast to pr
Autor:
Wang, Meizi, Li, Xinlu, Chen, Mengting, Wu, Xiaoqing, Mi, Yiduo, Kai, Zhenpeng, Yang, Xinling
Publikováno v:
In Bioorganic & Medicinal Chemistry Letters 1 April 2019 29(7):890-895
Autor:
Yecheng Liu, Kai Zhenpeng, Jiaxin Cui, Rui Zeng, Zhao Zhao, Zhonghua Wang, Fanhong Wu, Chao Fang, Yan Yin, Heng Zhang
Publikováno v:
Chinese Journal of Chemistry. 34:801-808
HMG-CoA reductase inhibitors were widely used as lipid-lowing agents through effectively blocking the rate-limiting step of cholesterol biosynthesis. 8 analogs of Rosuvastatin were firstly prepared with different distance and functional group between
Publikováno v:
Chinese Chemical Letters. 26:993-999
A total of 11 novel combretastatin A-4 (CA-4) analogs were designed, synthesized, and evaluated for the anti-proliferative effects in tumor cells. The compounds represent four structural classes: (i) hydrogenated derivatives, (ii) ethoxyl derivatives