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Dianqing Sun

Showing results (41-50 of 49) with videos related to

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Bioorganic & Medicinal Chemistry|December 9, 2009
Identification of triazinoindol-benzimidazolones as nanomolar inhibitors of the Mycobacterium tuberculosis enzyme TDP-6-deoxy-d-xylo-4-hexopyranosid-4-ulose 3,5-epimerase (RmlC)Sharmila Sivendran, Victoria Jones, Dianqing Sun, et al.
Journal of Natural Products|February 19, 2014
Herbicidin congeners, undecose nucleosides from an organic extract of Streptomyces sp. L-9-10Xingyun Chai, Ui Joung Youn, Dianqing Sun, et al.
Bioorganic & Medicinal Chemistry|April 24, 2009
Discovery, synthesis, and biological evaluation of piperidinol analogs with anti-tuberculosis activityDianqing Sun, Michael S Scherman, Victoria Jones, et al.
Plos One|February 23, 2019
Mechanism and resistance for antimycobacterial activity of a fluoroquinophenoxazine compoundPamela K Garcia, Thirunavukkarasu Annamalai, Wenjie Wang, et al.
ACS Omega|January 8, 2019
Pharmacophore Modeling, Synthesis, and Antibacterial Evaluation of Chalcones and DerivativesMingming Zhang, Allan M Prior, Marcus M Maddox, et al.
Bioorganic & Medicinal Chemistry|August 16, 2011
The structure-activity relationship of urea derivatives as anti-tuberculosis agentsJoshua R Brown, Elton J North, Julian G Hurdle, et al.
Journal of Medicinal Chemistry|September 3, 2015
Hirsutinolide Series Inhibit Stat3 Activity, Alter GCN1, MAP1B, Hsp105, G6PD, Vimentin, TrxR1, and Importin α-2 Expression, and Induce Antitumor Effects against Human GliomaGabriella Miklossy, Ui Joung Youn, Peibin Yue, et al.
Journal of Medicinal Chemistry|September 20, 2014
Synthesis, structure-activity relationship studies, and antibacterial evaluation of 4-chromanones and chalcones, as well as olympicin A and derivativesLi Feng, Marcus M Maddox, Md Zahidul Alam, et al.
Nature Medicine|January 28, 2014
Spectinamides: a new class of semisynthetic antituberculosis agents that overcome native drug effluxRichard E Lee, Julian G Hurdle, Jiuyu Liu, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Bioorganic & Medicinal Chemistry|December 9, 2009
Identification of triazinoindol-benzimidazolones as nanomolar inhibitors of the Mycobacterium tuberculosis enzyme TDP-6-deoxy-d-xylo-4-hexopyranosid-4-ulose 3,5-epimerase (RmlC)Sharmila Sivendran, Victoria Jones, Dianqing Sun, et al.
Journal of Natural Products|February 19, 2014
Herbicidin congeners, undecose nucleosides from an organic extract of Streptomyces sp. L-9-10Xingyun Chai, Ui Joung Youn, Dianqing Sun, et al.
Bioorganic & Medicinal Chemistry|April 24, 2009
Discovery, synthesis, and biological evaluation of piperidinol analogs with anti-tuberculosis activityDianqing Sun, Michael S Scherman, Victoria Jones, et al.
Plos One|February 23, 2019
Mechanism and resistance for antimycobacterial activity of a fluoroquinophenoxazine compoundPamela K Garcia, Thirunavukkarasu Annamalai, Wenjie Wang, et al.
ACS Omega|January 8, 2019
Pharmacophore Modeling, Synthesis, and Antibacterial Evaluation of Chalcones and DerivativesMingming Zhang, Allan M Prior, Marcus M Maddox, et al.
Bioorganic & Medicinal Chemistry|August 16, 2011
The structure-activity relationship of urea derivatives as anti-tuberculosis agentsJoshua R Brown, Elton J North, Julian G Hurdle, et al.
Journal of Medicinal Chemistry|September 3, 2015
Hirsutinolide Series Inhibit Stat3 Activity, Alter GCN1, MAP1B, Hsp105, G6PD, Vimentin, TrxR1, and Importin α-2 Expression, and Induce Antitumor Effects against Human GliomaGabriella Miklossy, Ui Joung Youn, Peibin Yue, et al.
Journal of Medicinal Chemistry|September 20, 2014
Synthesis, structure-activity relationship studies, and antibacterial evaluation of 4-chromanones and chalcones, as well as olympicin A and derivativesLi Feng, Marcus M Maddox, Md Zahidul Alam, et al.
Nature Medicine|January 28, 2014
Spectinamides: a new class of semisynthetic antituberculosis agents that overcome native drug effluxRichard E Lee, Julian G Hurdle, Jiuyu Liu, et al.
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