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MedChemComm

Showing results (401-410 of 801) with videos related to

Pageof 81
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Medchemcomm|June 24, 2015
Synthesis and evaluation of [<sup>11</sup>C]PBD150, a radiolabeled glutaminyl cyclase inhibitor for the potential detection of Alzheimer's disease prior to amyloid β aggregationAllen F Brooks, Isaac M Jackson, Xia Shao, et al.
Medchemcomm|January 9, 2018
Histone lysine methyltransferase structure activity relationships that allow for segregation of G9a inhibition and anti-<i>Plasmodium</i> activitySandeep Sundriyal, Patty B Chen, Alexandra S Lubin, et al.
Medchemcomm|March 13, 2018
Phenylethynyl-substituted Heterocycles Inhibit Cyclin D1 and Induce the Expression of Cyclin-dependent Kinase Inhibitor p21<sup>Wif1/Cip1</sup> in Colorectal Cancer CellsVitaliy M Sviripa, Liliia M Kril, Wen Zhang, et al.
Medchemcomm|December 19, 2017
Bitopic fluorescent antagonists of the A<sub>2A</sub> adenosine receptor based on pyrazolo[4,3-<i>e</i>][1,2,4]triazolo[1,5-<i>c</i>]pyrimidin-5-amine functionalized congenersRomain Duroux, Antonella Ciancetta, Philip Mannes, et al.
Medchemcomm|December 21, 2018
Synthesis and biological evaluation of 3-(1,3,4-oxadiazol-2-yl)-1,8-naphthyridin-4(1<i>H</i>)-ones as cisplatin sensitizersXueyan Hou, Hao Luo, Mengqi Zhang, et al.
Medchemcomm|December 21, 2018
The emerging chemical patterns applied in predicting human toll-like receptor 8 agonistsShuheng Huang, Hu Mei, Duo Zhang, et al.
Medchemcomm|August 17, 2016
Design, synthesis and evaluation of novel <sup>19</sup>F magnetic resonance sensitive protein tyrosine phosphatase inhibitorsYu Li, Guiquan Xia, Qi Guo, et al.
Medchemcomm|August 11, 2015
Synthesis and evaluation of a series of resveratrol analogues as potent anti-cancer agents that target tubulinNikhil R Madadi, Hongliang Zong, Amit Ketkar, et al.
Medchemcomm|August 4, 2015
Structure-Based Design, Synthesis by Click Chemistry and <i>in Vivo</i> Activity of Highly Selective A<sub>3</sub> Adenosine Receptor AgonistsDilip K Tosh, Silvia Paoletta, Zhoumou Chen, et al.
Medchemcomm|December 19, 2015
The design and synthesis of 5- and 6-isoxazolylbenzimidazoles as selective inhibitors of the BET bromodomainsDuncan Hay, Oleg Fedorov, Panagis Filippakopoulos, et al.
Pageof 81

Showing results (401-410 of 801) with videos related to

Sort By:
Pageof 81
Medchemcomm|June 24, 2015
Synthesis and evaluation of [<sup>11</sup>C]PBD150, a radiolabeled glutaminyl cyclase inhibitor for the potential detection of Alzheimer's disease prior to amyloid β aggregationAllen F Brooks, Isaac M Jackson, Xia Shao, et al.
Medchemcomm|January 9, 2018
Histone lysine methyltransferase structure activity relationships that allow for segregation of G9a inhibition and anti-<i>Plasmodium</i> activitySandeep Sundriyal, Patty B Chen, Alexandra S Lubin, et al.
Medchemcomm|March 13, 2018
Phenylethynyl-substituted Heterocycles Inhibit Cyclin D1 and Induce the Expression of Cyclin-dependent Kinase Inhibitor p21<sup>Wif1/Cip1</sup> in Colorectal Cancer CellsVitaliy M Sviripa, Liliia M Kril, Wen Zhang, et al.
Medchemcomm|December 19, 2017
Bitopic fluorescent antagonists of the A<sub>2A</sub> adenosine receptor based on pyrazolo[4,3-<i>e</i>][1,2,4]triazolo[1,5-<i>c</i>]pyrimidin-5-amine functionalized congenersRomain Duroux, Antonella Ciancetta, Philip Mannes, et al.
Medchemcomm|December 21, 2018
Synthesis and biological evaluation of 3-(1,3,4-oxadiazol-2-yl)-1,8-naphthyridin-4(1<i>H</i>)-ones as cisplatin sensitizersXueyan Hou, Hao Luo, Mengqi Zhang, et al.
Medchemcomm|December 21, 2018
The emerging chemical patterns applied in predicting human toll-like receptor 8 agonistsShuheng Huang, Hu Mei, Duo Zhang, et al.
Medchemcomm|August 17, 2016
Design, synthesis and evaluation of novel <sup>19</sup>F magnetic resonance sensitive protein tyrosine phosphatase inhibitorsYu Li, Guiquan Xia, Qi Guo, et al.
Medchemcomm|August 11, 2015
Synthesis and evaluation of a series of resveratrol analogues as potent anti-cancer agents that target tubulinNikhil R Madadi, Hongliang Zong, Amit Ketkar, et al.
Medchemcomm|August 4, 2015
Structure-Based Design, Synthesis by Click Chemistry and <i>in Vivo</i> Activity of Highly Selective A<sub>3</sub> Adenosine Receptor AgonistsDilip K Tosh, Silvia Paoletta, Zhoumou Chen, et al.
Medchemcomm|December 19, 2015
The design and synthesis of 5- and 6-isoxazolylbenzimidazoles as selective inhibitors of the BET bromodomainsDuncan Hay, Oleg Fedorov, Panagis Filippakopoulos, et al.
Pageof 81