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Methods in Molecular Biology (Clifton, N.J.)|October 24, 2019
LC/MS Methods for Studying Lysosomal ADC CatabolismAndrew J Bessire, Chakrapani Subramanyam
ACS Medicinal Chemistry Letters|August 16, 2019
Quick Building Blocks (QBB): An Innovative and Efficient Business Model To Speed Medicinal Chemistry Analog SynthesisChristopher J Helal, Mark Bundesmann, Susan Hammond, et al.
Bioconjugate Chemistry|May 22, 2016
Determination of Antibody-Drug Conjugate Released Payload Species Using Directed in Vitro Assays and Mass Spectrometric InterrogationAndrew J Bessire, T Eric Ballard, Manoj Charati, et al.
Bioorganic & Medicinal Chemistry Letters|July 26, 2011
Discovery, synthesis and SAR of azinyl- and azolylbenzamides antagonists of the P2X₇ receptorChakrapani Subramanyam, Allen J Duplantier, Mark A Dombroski, et al.
Cell Chemical Biology|November 20, 2018
Covalent Docking Identifies a Potent and Selective MKK7 InhibitorAmit Shraga, Evgenia Olshvang, Natalia Davidzohn, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 21, 2011
Quantitative pharmacokinetic/pharmacodynamic analyses suggest that the 129/SVE mouse is a suitable preclinical pharmacology model for identifying small-molecule γ-secretase inhibitorsYasong Lu, Liming Zhang, Charles E Nolan, et al.
ACS Chemical Neuroscience|June 14, 2017
Identification and Profiling of a Selective and Brain Penetrant Radioligand for in Vivo Target Occupancy Measurement of Casein Kinase 1 (CK1) InhibitorsTravis T Wager, Paul Galatsis, Ramalakshmi Y Chandrasekaran, et al.
ACS Medicinal Chemistry Letters|November 25, 2016
Design, Synthesis, and Cytotoxic Evaluation of Novel Tubulysin Analogues as ADC PayloadsCarolyn A Leverett, Sai Chetan K Sukuru, Beth C Vetelino, et al.
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