Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Qiong Gu

Showing results (61-70 of 216) with videos related to

Pageof 22
Sort By:
Journal of Natural Products|April 3, 2020
Jatrophane Diterpenoids from <i>Euphorbia esula</i> as Inhibitors of RANKL-Induced OsteoclastogenesisShengheng Yuan, Pei Hua, Chao Zhao, et al.
Fitoterapia|June 11, 2022
Diverse polyacetylenes from Atractylodes chinensis and their anti-osteoclastogenesis activityYuting Zhang, Xing Peng, Zhejun Sun, et al.
Journal of Natural Products|August 11, 2023
Discovery of <i>neo</i>-Clerodane Diterpenoids from <i>Ajuga campylantha</i> as Neuroprotective Agents against Ferroptosis and NeuroinflammationXing Peng, Qingyun Tan, Zhikang Zhang, et al.
Chemical Biology & Drug Design|May 12, 2015
Synthesis and anti-neuroinflammatory activity of lactone benzoyl hydrazine and 2-nitro-1-phenyl-1h-indole derivatives as p38α MAPK inhibitorsBao Cheng, Yongsheng Lin, Ming Kuang, et al.
Acta Crystallographica. Section E, Structure Reports Online|May 18, 2011
Bis[4-amino-N-(pyrimidin-2-yl)benzene-sulfonamidato](2,2'-bipyridine)manganese(II)Tian-Jing He, Yan-Shu Tan, Yun-Qiong Gu, et al.
Fitoterapia|January 29, 2018
Ethylnaphthoquinone derivatives as inhibitors of indoleamine-2, 3-dioxygenase from the mangrove endophytic fungus Neofusicoccum austral SYSU-SKS024Hui Cui, Hongao Zhang, Yena Liu, et al.
Journal of Cheminformatics|January 19, 2019
QBMG: quasi-biogenic molecule generator with deep recurrent neural networkShuangjia Zheng, Xin Yan, Qiong Gu, et al.
Journal of Medicinal Chemistry|September 28, 2016
Incorporation of Privileged Structures into Bevirimat Can Improve Activity against Wild-Type and Bevirimat-Resistant HIV-1Yu Zhao, Qiong Gu, Susan L Morris-Natschke, et al.
Dalton Transactions (Cambridge, England : 2003)|January 6, 2022
Ru(III) complexes with pyrazolopyrimidines as anticancer agents: bioactivities and the underlying mechanismsYun-Qiong Gu, Wen-Ying Shen, Qi-Yuan Yang, et al.
Journal of Medicinal Chemistry|December 20, 2022
Discovery of Spiro[pyrrolidine-3,3'-oxindole] LXRβ Agonists for the Treatment of OsteoporosisHao Chen, Pei Hua, Dane Huang, et al.
Pageof 22

Showing results (61-70 of 216) with videos related to

Sort By:
Pageof 22
Journal of Natural Products|April 3, 2020
Jatrophane Diterpenoids from <i>Euphorbia esula</i> as Inhibitors of RANKL-Induced OsteoclastogenesisShengheng Yuan, Pei Hua, Chao Zhao, et al.
Fitoterapia|June 11, 2022
Diverse polyacetylenes from Atractylodes chinensis and their anti-osteoclastogenesis activityYuting Zhang, Xing Peng, Zhejun Sun, et al.
Journal of Natural Products|August 11, 2023
Discovery of <i>neo</i>-Clerodane Diterpenoids from <i>Ajuga campylantha</i> as Neuroprotective Agents against Ferroptosis and NeuroinflammationXing Peng, Qingyun Tan, Zhikang Zhang, et al.
Chemical Biology & Drug Design|May 12, 2015
Synthesis and anti-neuroinflammatory activity of lactone benzoyl hydrazine and 2-nitro-1-phenyl-1h-indole derivatives as p38α MAPK inhibitorsBao Cheng, Yongsheng Lin, Ming Kuang, et al.
Acta Crystallographica. Section E, Structure Reports Online|May 18, 2011
Bis[4-amino-N-(pyrimidin-2-yl)benzene-sulfonamidato](2,2'-bipyridine)manganese(II)Tian-Jing He, Yan-Shu Tan, Yun-Qiong Gu, et al.
Fitoterapia|January 29, 2018
Ethylnaphthoquinone derivatives as inhibitors of indoleamine-2, 3-dioxygenase from the mangrove endophytic fungus Neofusicoccum austral SYSU-SKS024Hui Cui, Hongao Zhang, Yena Liu, et al.
Journal of Cheminformatics|January 19, 2019
QBMG: quasi-biogenic molecule generator with deep recurrent neural networkShuangjia Zheng, Xin Yan, Qiong Gu, et al.
Journal of Medicinal Chemistry|September 28, 2016
Incorporation of Privileged Structures into Bevirimat Can Improve Activity against Wild-Type and Bevirimat-Resistant HIV-1Yu Zhao, Qiong Gu, Susan L Morris-Natschke, et al.
Dalton Transactions (Cambridge, England : 2003)|January 6, 2022
Ru(III) complexes with pyrazolopyrimidines as anticancer agents: bioactivities and the underlying mechanismsYun-Qiong Gu, Wen-Ying Shen, Qi-Yuan Yang, et al.
Journal of Medicinal Chemistry|December 20, 2022
Discovery of Spiro[pyrrolidine-3,3'-oxindole] LXRβ Agonists for the Treatment of OsteoporosisHao Chen, Pei Hua, Dane Huang, et al.
Pageof 22