Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Xiangguo, Meng"'
Publikováno v:
Frontiers in Pharmacology, Vol 10 (2019)
In this study, the absorption, distribution, metabolism and excretion (ADME) of sodium danshensu (Sodium DL-β-(3, 4-dihydroxyphenyl)lactate), one of the main water-soluble active constituents in Salvia miltiorrhiza, were evaluated in rats. Pharmacok
Externí odkaz:
https://doaj.org/article/6636d8c2632c462f9ff02bb261f9a8cd
Publikováno v:
International Journal of Theoretical Physics. 61
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a835f7f128f65131f04443a645a941b9
https://doi.org/10.1007/s10773-022-05248-x
https://doi.org/10.1007/s10773-022-05248-x
Publikováno v:
2022 IEEE 10th Asia-Pacific Conference on Antennas and Propagation (APCAP).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::caf1f8752530599030bab3aabee3c2ea
https://doi.org/10.1109/apcap56600.2022.10069137
https://doi.org/10.1109/apcap56600.2022.10069137
Autor:
Jing-Gen Liu, Xiangguo Meng, Jing Liu, Wenli Wang, Huoming Huang, Jing-Rui Chai, Jing Chen, Wei Li, Xue-Ping Li, Congmin Yuan, Wei Fu, Xinwei Li, Xue-Jun Xu, Peng Xie, Yujun Wang, Yuanyuan Qian
Publikováno v:
Journal of Medicinal Chemistry. 64:9458-9483
Management of moderate to severe pain relies heavily on opioid analgesics such as morphine, oxycodone, and fentanyl in clinics. However, their prolonged use was associated with undesirable side effects. Many new strategies to reduce side effects have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f906863e262826f49cc9db2fb0b05e0
https://doi.org/10.1021/acs.jmedchem.1c00722
https://doi.org/10.1021/acs.jmedchem.1c00722
Autor:
Xiangguo Meng, Siju Bi, Shixin Jin, Kai Wu, Shanchao Wu, Lei Shao, Pierre-Antoine Bonnet, Chunquan Sheng
Publikováno v:
Chinese Chemical Letters. 34:108096
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fef87dc7e9c7fe13e17cad1f25aa48ce
https://doi.org/10.1016/j.cclet.2022.108096
https://doi.org/10.1016/j.cclet.2022.108096
Publikováno v:
Evidence-based complementary and alternative medicine : eCAM. 2022
Type 2 diabetes mellitus (T2DM) has been regarded as a critical risk factor for pulmonary tuberculosis (PTB). Ginsenoside Rg1 has been identified as a potential therapeutic agent for T2DM by suppressing the inflammatory response. However, the effect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dee8a9e5362d3b1455be7e5506864d1
https://pubmed.ncbi.nlm.nih.gov/36248428
https://pubmed.ncbi.nlm.nih.gov/36248428
Publikováno v:
2022 China Semiconductor Technology International Conference (CSTIC).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3eba416dccedea372dc328e1b26781bf
https://doi.org/10.1109/cstic55103.2022.9856786
https://doi.org/10.1109/cstic55103.2022.9856786
Publikováno v:
Catalysis Science & Technology. 10:1650-1660
Steric hindrance in the binding pocket of an alcohol dehydrogenase (ADH) has a great impact on its activity and stereoselectivity simultaneously. Due to the subtle structural difference between two bulky phenyl substituents, the asymmetric synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45ec3b930a4c8964c5413b585be7d440
https://doi.org/10.1039/c9cy02444a
https://doi.org/10.1039/c9cy02444a
Publikováno v:
Bioorganic chemistry. 122
On the basis of synergistic effect between topoisomerase (Top) and histone deacetylase (HDAC) inhibitors, a series of novel evodiamine-based Top/HDAC dual inhibitors were designed and synthesized. Systematic structure-activity relationship (SAR) stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::755b10843ab5d10dcf12d582775332ea
https://pubmed.ncbi.nlm.nih.gov/35286923
https://pubmed.ncbi.nlm.nih.gov/35286923
Publikováno v:
Applied Microbiology and Biotechnology. 103:4417-4427
(2R,3S)-N-tert-Butoxycarbonyl-3-amino-1-chloro-2-hydroxy-4-phenylbutane (1b) is key for the synthesis of the antiviral drug atazanavir. It can be obtained via the stereoselective bioreduction of (3S)-3-(N-Boc-amino)-1-chloro-4-phenyl-butanone (1a) wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6235728893c0a627b9d48945bb22f4c
https://doi.org/10.1007/s00253-019-09781-4
https://doi.org/10.1007/s00253-019-09781-4