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Journal of Medicinal Chemistry
|
January 28, 2021
Correction to "Identification of 2,4-Disubstituted Imidazopyridines as Hemozoin Formation Inhibitors with Fast-Killing Kinetics and <i>In Vivo</i> Efficacy in the <i>Plasmodium falciparum</i> NSG Mouse Model"
André Horatscheck, Ana Andrijevic, Aloysius T Nchinda, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 4, 2011
Pyrimido[4,5-d]azepines as potent and selective 5-HT2C receptor agonists: design, synthesis, and evaluation of PF-3246799 as a treatment for urinary incontinence
Mark D Andrews, Paul V Fish, Julian Blagg, et al.
ACS Chemical Biology
|
August 30, 2017
Selective Targeting of Bromodomains of the Bromodomain-PHD Fingers Family Impairs Osteoclast Differentiation
Julia C Meier, Cynthia Tallant, Oleg Fedorov, et al.
Nature
|
June 3, 2021
NOTUM from Apc-mutant cells biases clonal competition to initiate cancer
Dustin J Flanagan, Nalle Pentinmikko, Kalle Luopajärvi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 20, 2014
(R)-PFI-2 is a potent and selective inhibitor of SETD7 methyltransferase activity in cells
Dalia Barsyte-Lovejoy, Fengling Li, Menno J Oudhoff, et al.
Antimicrobial Agents and Chemotherapy
|
June 27, 2018
UCT943, a Next-Generation Plasmodium falciparum PI4K Inhibitor Preclinical Candidate for the Treatment of Malaria
Christel Brunschwig, Nina Lawrence, Dale Taylor, et al.
Antimicrobial Agents and Chemotherapy
|
October 26, 2018
Erratum for Brunschwig et al., "UCT943, a Next-Generation Plasmodium falciparum PI4K Inhibitor Preclinical Candidate for the Treatment of Malaria"
Christel Brunschwig, Nina Lawrence, Dale Taylor, et al.
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Search research articles
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Showing results (51-60 of 57) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 57 results.
Journal of Medicinal Chemistry
|
January 28, 2021
Correction to "Identification of 2,4-Disubstituted Imidazopyridines as Hemozoin Formation Inhibitors with Fast-Killing Kinetics and <i>In Vivo</i> Efficacy in the <i>Plasmodium falciparum</i> NSG Mouse Model"
André Horatscheck, Ana Andrijevic, Aloysius T Nchinda, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 4, 2011
Pyrimido[4,5-d]azepines as potent and selective 5-HT2C receptor agonists: design, synthesis, and evaluation of PF-3246799 as a treatment for urinary incontinence
Mark D Andrews, Paul V Fish, Julian Blagg, et al.
ACS Chemical Biology
|
August 30, 2017
Selective Targeting of Bromodomains of the Bromodomain-PHD Fingers Family Impairs Osteoclast Differentiation
Julia C Meier, Cynthia Tallant, Oleg Fedorov, et al.
Nature
|
June 3, 2021
NOTUM from Apc-mutant cells biases clonal competition to initiate cancer
Dustin J Flanagan, Nalle Pentinmikko, Kalle Luopajärvi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 20, 2014
(R)-PFI-2 is a potent and selective inhibitor of SETD7 methyltransferase activity in cells
Dalia Barsyte-Lovejoy, Fengling Li, Menno J Oudhoff, et al.
Antimicrobial Agents and Chemotherapy
|
June 27, 2018
UCT943, a Next-Generation Plasmodium falciparum PI4K Inhibitor Preclinical Candidate for the Treatment of Malaria
Christel Brunschwig, Nina Lawrence, Dale Taylor, et al.
Antimicrobial Agents and Chemotherapy
|
October 26, 2018
Erratum for Brunschwig et al., "UCT943, a Next-Generation Plasmodium falciparum PI4K Inhibitor Preclinical Candidate for the Treatment of Malaria"
Christel Brunschwig, Nina Lawrence, Dale Taylor, et al.
Page
of 6