Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Lianbo Zhao"'
Autor:
Cen Xiang, Quanyuan Qiu, Chunmei Zhang, Yandong Leng, Mengzhen Yuan, Yao Rong, Futao Liu, Lianbo Zhao, Zhen Liu, Yunsong Chang, Yu-Ou Teng
Publikováno v:
European Journal of Medicinal Chemistry Reports, Vol 12, Iss , Pp 100196- (2024)
Flavonoids are widely found in plants and diets and are considered to possess a variety of biological activities. Therefore, in this study, 8 novel compounds derivating from the precursor compound 1a, were designed and synthesized, and their activiti
Externí odkaz:
https://doaj.org/article/24824b2d79d04389ba41eafe8219511c
Autor:
Zhen Liu, Ye Xu, Lvqian Guo, Xinran Li, Junling Gao, Weiran Xie, Lianbo Zhao, Yuou Teng, Xuejiao Li, Peng Yu
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 38, Iss 1, Pp 1-11 (2023)
The effect of the combination of 10-Hydroxycamptothecin (HCPT) and crizotinib (CRI) on EGFR- and KRAS-mutant lung cancer cells was investigated and the conjugates of the two drugs were synthesised. HCPT combined with CRI synergistically inhibited the
Externí odkaz:
https://doaj.org/article/51b38f276eb046cd8373dae2a520c22f
Publikováno v:
Molecules, Vol 26, Iss 16, p 4779 (2021)
(±)-Anastatins A and B are flavonoids isolated from Anastatica hierochuntica. In a previous study, twenty-four di- and tri-substituted novel derivatives of anastatins were designed and their preliminary antioxidant activities were evaluated. In the
Externí odkaz:
https://doaj.org/article/21528f08e1294c27a9723209261b53dd
Publikováno v:
Molecules, Vol 26, Iss 1, p 176 (2020)
A series of multi-substituted isatin derivatives were synthesized using the powerful Sandmeyer reaction. The structures of these derivatives were confirmed by 1H-NMR, 13C-NMR, and HR-MS. Inhibition of proliferation activities of these derivatives aga
Externí odkaz:
https://doaj.org/article/08397027d6ee4fc0ad27897cbb6ada7f
Autor:
Cen Xiang, Xiaoxuan Chen, Jiaping Yao, Na Yang, Jiajia Yu, Quanyuan Qiu, Shouqing Zhang, Xiangsun Kong, Lianbo Zhao, Zhen-chuan Fan, Peng Yu, Yuou Teng
Publikováno v:
European Journal of Medicinal Chemistry. :115510
Publikováno v:
Molecules, Vol 26, Iss 176, p 176 (2021)
Molecules
Volume 26
Issue 1
Molecules
Volume 26
Issue 1
A series of multi-substituted isatin derivatives were synthesized using the powerful Sandmeyer reaction. The structures of these derivatives were confirmed by 1H-NMR, 13C-NMR, and HR-MS. Inhibition of proliferation activities of these derivatives aga
Publikováno v:
Molecules, Vol 26, Iss 4779, p 4779 (2021)
Molecules
Volume 26
Issue 16
Molecules
Volume 26
Issue 16
(±)-Anastatins A and B are flavonoids isolated from Anastatica hierochuntica. In a previous study, twenty-four di- and tri-substituted novel derivatives of anastatins were designed and their preliminary antioxidant activities were evaluated. In the
Autor:
Qian Zhang, Yuning Liu, Na Guo, Lianbo Zhao, Peng Yu, Tao Zhu, Tiantian Hao, Xin Meng, Jiacheng Liu, Haomeng Wang
Publikováno v:
Carbohydrate research. 499
Brucellosis is a highly infectious zoonotic disease caused by Brucella. It is necessary to control and eliminate brucellosis. The cell wall O-polysaccharides of pathogenic Brucella species are homopolymers of the rare sugar 4,6-dideoxy-4-formamido-α
Publikováno v:
Advanced Synthesis and Catalysis
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2020, 362 (18), pp.3841-3845. ⟨10.1002/adsc.202000769⟩
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2020, 362 (18), pp.3841-3845. ⟨10.1002/adsc.202000769⟩
International audience; A concise and practical method for the metal-free synthesis of 1,8-naphthyridones is described using a two-step approach involving regioselective amination of pyridine N-oxides and acid-mediated cyclization. This is the first
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b35a57bca4f57d77ca84a7fa397d3e3
https://hal.archives-ouvertes.fr/hal-02996754
https://hal.archives-ouvertes.fr/hal-02996754
Autor:
Lianbo Zhao, Xinying Zhang, Yinan Zhang, Robert H. Dodd, Hao Lei, Yujiao Ma, Hua Sun, Peng Yu, Ying Ma
Publikováno v:
Bioorganicmedicinal chemistry letters. 30(14)
A series of tetracyclic oxindole derivatives was synthesized by asymmetric 1, 3-dipole reaction in 2–4 steps in 57–86% overall yields. These compounds were evaluated for α-glucosidase inhibitory and glucose consumption-promoting activity in vitr