Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Danmei Tian"'
Autor:
Fangfang Wang, Sora Jin, Franklin Mayca Pozo, Danmei Tian, Xiyang Tang, Yi Dai, Xinsheng Yao, Jinshan Tang, Youwei Zhang
Publikováno v:
Acta Pharmaceutica Sinica B, Vol 12, Iss 3, Pp 1339-1350 (2022)
DNA damage response (DDR) is a highly conserved genome surveillance mechanism that preserves cell viability in the presence of chemotherapeutic drugs. Hence, small molecules that inhibit DDR are expected to enhance the anti-cancer effect of chemother
Externí odkaz:
https://doaj.org/article/8072e7df692147dfa21278fcaad7299d
Autor:
Shanji Chen, Danmei Tian, Jihua Wei, Cong Li, Yihan Ma, Xiaoshuang Gou, Yiran Shen, Mei Chen, Sihao Zhang, Jia Li, Bin Wu, Jinshan Tang
Publikováno v:
Frontiers in Marine Science, Vol 9 (2022)
Two new citrinin dimers bearing a 6,6-spiroketal moiety (1 and 2) and four known analogues (3–6), together with 18 known citrinin monomers (7–24), were isolated from the culture of hydrothermal vent-associated fungus Penicillium citrinum Y34. The
Externí odkaz:
https://doaj.org/article/4d6149c6e9254c798132c7007c3bee46
Autor:
Changrong Lai, Jiayi Chen, Jing Liu, Danmei Tian, Donghe Lan, Tongzheng Liu, Bin Wu, Hongkai Bi, Jinshan Tang
Publikováno v:
Marine Drugs, Vol 20, Iss 11, p 720 (2022)
Marine fungi-derived secondary metabolites are still an important source for the discovery of potential antimicrobial agents. Here, five new polyketides (1, 2, and 6–8) and seven known compounds (3–5 and 9–12) were obtained from the culture of
Externí odkaz:
https://doaj.org/article/f1a975c37e4b4f8d9031d185beab2e4d
Autor:
Fangfang Wang, Franklin Mayca Pozo, Danmei Tian, Xinran Geng, Xinsheng Yao, Youwei Zhang, Jinshan Tang
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2020)
Externí odkaz:
https://doaj.org/article/232e2c3e6c6241b195eb499f1fe693df
Autor:
Fangfang Wang, Franklin Mayca Pozo, Danmei Tian, Xinran Geng, Xinsheng Yao, Youwei Zhang, Jinshan Tang
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2020)
Shikonin is a natural naphthoquinone compound and has demonstrated potent anti-cancer activities; however, the underlying molecular mechanisms remained elusive. Here we report that Shikonin inhibited the growth of a wide range of human cancer cell li
Externí odkaz:
https://doaj.org/article/98cdc45294c840fe9e6249602c419b83
Autor:
Xiaoshuang Gou, Danmei Tian, Jihua Wei, Yihan Ma, Yixue Zhang, Mei Chen, Wenjuan Ding, Bin Wu, Jinshan Tang
Publikováno v:
Marine Drugs, Vol 19, Iss 8, p 416 (2021)
Marine fungi-derived natural products represent an excellent reservoir for the discovery of novel lead compounds with biological activities. Here, we report the identification of two new drimane sesquiterpenes (1 and 2) and six new polyketides (3–8
Externí odkaz:
https://doaj.org/article/354794d396164bb18e4a8c86f4a60165
Autor:
Wenjuan Ding, Chokkalingam Uvarani, Fangfang Wang, Yaxin Xue, Ning Wu, Liming He, Danmei Tian, Mei Chen, Youwei Zhang, Kui Hong, Jinshan Tang
Publikováno v:
Marine Drugs, Vol 18, Iss 11, p 575 (2020)
Deep-sea fungi have become a new arsenal for the discovery of leading compounds. Here five new ophiobolins 1–5, together with six known analogues 6–11, obtained from a deep-sea derived fungus WHU0154. Their structures were determined by analyses
Externí odkaz:
https://doaj.org/article/5841bd89b22a40558bbfb8a554f041bf
Publikováno v:
Fitoterapia. 162
A new pentacyclic triterpenoid, 2-hydroxy-1-ene-hydroxyhopanone (19), and a new benzoxepin-5-one, 3-(4-methyl-3-penten-1-yl)-6-hydroxy-9-methoxy-2H-1-benzoxepin-5-one (25), along with 26 known compounds (1-18, 20-24, 26-28), were isolated from the ro
Autor:
Danmei Tian, Huadong Zhao, Jing Cao, Sihao Zhang, Wanqi Wang, Xiyang Tang, Yi Dai, Wangyi Zhou, Lihua Zhang, Jiefeng Tian, Yuanyuan Han, Jinshan Tang, Zhaohui Song, Xiaohui Ma, Yi He, Xinsheng Yao
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 227:115271
Autor:
Xin-Sheng Yao, Xinran Geng, Qingwen Li, Jinshan Tang, Youwei Zhang, Fangfang Wang, Danmei Tian, Goutham Narla, Huadong Zhao
Publikováno v:
Cancer Lett
Kirsten rat sarcoma virus oncogene homolog (KRAS) mutant lung cancer remains a challenge to cure and chemotherapy is the current standard treatment in the clinic. Hence, understanding molecular mechanisms underlying the sensitivity of KRAS mutant lun