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Current Opinion in Investigational Drugs (London, England : 2000)|February 7, 2004
Farnesyltransferase inhibitors as anticancer agents: current statusKuichun Zhu, Andrew D Hamilton, Saïd M SebtiRSC Advances|November 29, 2023
Tetrazole and acylsulfonamide bioisosteric replacements of the carboxylic acid in a dual MCL-1/BCL-x<sub>L</sub> inhibitor are toleratedLijia Chen, Brandon Lowe, Steven FletcherChemistry & Biology|February 28, 2009
Structural basis for binding and selectivity of antimalarial and anticancer ethylenediamine inhibitors to protein farnesyltransferaseMichael A Hast, Steven Fletcher, Christopher G Cummings, et al.Current Topics in Microbiology and Immunology|September 10, 2010
Hydrogen-bonded synthetic mimics of protein secondary structure as disruptors of protein-protein interactionsMarc J Adler, Andrew G Jamieson, Andrew D HamiltonPhilosophical Transactions. Series A, Mathematical, Physical, and Engineering Sciences|February 4, 2010
Synthetic mimetics of protein secondary structure domainsNathan T Ross, William P Katt, Andrew D HamiltonBioorganic & Medicinal Chemistry Letters|July 5, 2005
Self-assembly of bivalent protein-binding agents based on oligonucleotide-linked organic fragmentsK Ingrid Sprinz, Debarati M Tagore, Andrew D HamiltonOrganic Letters|September 20, 2019
Heterofunctionalized Cavitands by Macrocyclization of Sequence-Defined FoldamersJoseph W Meisel, Chunhua T Hu, Andrew D HamiltonTetrahedron Letters|March 31, 2010
Combined solid/solution phase synthesis of large surface area scaffolds derived from aminomethyl-benzoatesRishi K Jain, Lun K Tsou, Andrew D HamiltonOrganic & Biomolecular Chemistry|October 2, 2009
Novel 7-(dimethylamino)fluorene-based fluorescent probes and their binding to human serum albuminKwanghee Koh Park, Joon Woo Park, Andrew D HamiltonChemical Communications (Cambridge, England)|February 24, 2010
Programing the formation of DNA and PNA quadruplexes by pi-pi-stacking interactionsSourav Saha, Jianfeng Cai, Daniel Eiler, et al.Pageof 26