Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Huqiang, Lv"'
Publikováno v:
Mitochondrial DNA. Part B. Resources, Vol 7, Iss 6, Pp 969-970 (2022)
Habenaria dentata is a rare species with high ornamental value in China. In this study, we report the complete chloroplast (cp) genome of H. dentata using the Illumina sequencing data. The total genome of H. dentata is 153,682 bp in length and the GC
Externí odkaz:
https://doaj.org/article/530f0750d5f44f99a66cfcb87f966cc1
Publikováno v:
Mitochondrial DNA. Part B. Resources, Vol 7, Iss 2, Pp 326-327 (2022)
Ficus pumila L. is a climbing fig commonly used as an ornamental plant. In this study, we sequenced and assembled the complete chloroplast genome of F. pumila. The complete chloroplast genome of F. pumila is 160,248 bp in length which includes a pair
Externí odkaz:
https://doaj.org/article/1684448d95f64036adaccfda445cdaaa
Autor:
Chengde Wu, Gong Zhen, Xijun Sheng, Chen Shuhui, Shoubo Zhang, Jie Shen, Huqiang Lv, Wang Xuehai, Jun Wang, Zhibo Qi, Hu Guoping, Sun Wenjie, Sun Guanglong, Yuchuan Zhu, Weifeng Mao, Liang Shen, Xuejun Zhang, Yan Pan, Minghui Cui, Ronghua Tu, Dongling Hao, Shuhua Han, Shen Chunli, Xin Li, Li Yi, Lei Huang, Jian Li
Publikováno v:
ACS Medicinal Chemistry Letters. 11:1863-1868
The identification and lead optimization of a series of pyrazolo[3,4-d]pyridazinone derivatives are described as a novel class of potent irreversible BTK inhibitors, resulting in the discovery of compound 8. Compound 8 exhibited high potency against
Autor:
Xuejun, Zhang, Xijun, Sheng, Jie, Shen, Shoubo, Zhang, Wenjie, Sun, Chunli, Shen, Yi, Li, Jun, Wang, Huqiang, Lv, Minghui, Cui, Yuchuan, Zhu, Lei, Huang, Dongling, Hao, Zhibo, Qi, Guanglong, Sun, Weifeng, Mao, Yan, Pan, Liang, Shen, Xin, Li, Guoping, Hu, Zhen, Gong, Shuhua, Han, Jian, Li, Shuhui, Chen, Ronghua, Tu, Xuehai, Wang, Chengde, Wu
Publikováno v:
ACS Med Chem Lett
[Image: see text] The identification and lead optimization of a series of pyrazolo[3,4-d]pyridazinone derivatives are described as a novel class of potent irreversible BTK inhibitors, resulting in the discovery of compound 8. Compound 8 exhibited hig