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Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|March 27, 2021
The histamine H3R and dopamine D2R/D3R antagonist ST-713 ameliorates autism-like behavioral features in BTBR T+tf/J mice by multiple actionsKarthikkumar Venkatachalam, Nermin Eissa, Mohamed Al Awad, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|July 9, 2008
A solid phase parallel synthesis of diverse amides as dopamine D3 receptor ligandsMickaël Jean, Jacques Renault, Jean-Claude Camelin, et al.
Nature Reviews. Drug Discovery|June 9, 2018
Cryo-EM in drug discovery: achievements, limitations and prospectsJean-Paul Renaud, Ashwin Chari, Claudio Ciferri, et al.
Nature|July 20, 2007
Structural insight into filament formation by mammalian septinsMinhajuddin Sirajuddin, Marian Farkasovsky, Florian Hauer, et al.
Bioorganic & Medicinal Chemistry|June 12, 2002
Piperidino-hydrocarbon compounds as novel non-imidazole histamine H(3)-receptor antagonistsGalina Meier, Xavier Ligneau, Heinz H Pertz, et al.
Bioorganic & Medicinal Chemistry|April 19, 2011
N-Alkenyl and cycloalkyl carbamates as dual acting histamine H3 and H4 receptor ligandsMałgorzata Więcek, Tim Kottke, Xavier Ligneau, et al.
Bioorganic & Medicinal Chemistry Letters|April 22, 2014
Benzylpiperidine variations on histamine H3 receptor ligands for improved drug-likenessKerstin Wingen, J Stephan Schwed, Kathleen Isensee, et al.
Nature Structural & Molecular Biology|December 28, 2010
Substrate binding on the APC/C occurs between the coactivator Cdh1 and the processivity factor Doc1Bettina A Buschhorn, Georg Petzold, Marta Galova, et al.
Science (New York, N.Y.)|August 6, 2016
The inhibition mechanism of human 20S proteasomes enables next-generation inhibitor designJil Schrader, Fabian Henneberg, Ricardo A Mata, et al.
British Journal of Pharmacology|February 28, 2018
Antinociceptive effects of novel histamine H3 and H4 receptor antagonists and their influence on morphine analgesia of neuropathic pain in the mouseKatarzyna Popiolek-Barczyk, Dorota Łażewska, Gniewomir Latacz, et al.
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