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Bioorganic & Medicinal Chemistry Letters|December 27, 2015
A minimally cytotoxic CD4 mimic as an HIV entry inhibitorTakaaki Mizuguchi, Shigeyoshi Harada, Tomoyuki Miura, et al.Bioorganic & Medicinal Chemistry|November 6, 2013
A CD4 mimic as an HIV entry inhibitor: pharmacokineticsChie Hashimoto, Tetsuo Narumi, Hiroyuki Otsuki, et al.Organic & Biomolecular Chemistry|August 27, 2009
Structure-activity relationship study on artificial CXCR4 ligands possessing the cyclic pentapeptide scaffold: the exploration of amino acid residues of pentapeptides by substitutions of several aromatic amino acidsTomohiro Tanaka, Wataru Nomura, Tetsuo Narumi, et al.Journal of Agricultural and Food Chemistry|January 26, 2016
Characteristic Fluctuations in Glycosidically Bound Volatiles during Tea Processing and Identification of Their Unstable DerivativesJilai Cui, Tsuyoshi Katsuno, Kojiro Totsuka, et al.Journal of Medicinal Chemistry|February 20, 2026
Amide-to-Chloroalkene Substitution for Peptide Backbone Modification to Enhance Membrane PermeabilitySayuri Takeo, Mio Takeda, Chihiro Iio, et al.Bioorganic & Medicinal Chemistry|August 17, 2010
Peptidic HIV integrase inhibitors derived from HIV gene products: structure-activity relationship studiesShintaro Suzuki, Kasthuraiah Maddali, Chie Hashimoto, et al.ACS Chemical Biology|August 1, 2013
Cell-permeable stapled peptides based on HIV-1 integrase inhibitors derived from HIV-1 gene productsWataru Nomura, Haruo Aikawa, Nami Ohashi, et al.Journal of Medicinal Chemistry|July 1, 2010
Peptide HIV-1 integrase inhibitors from HIV-1 gene productsShintaro Suzuki, Emiko Urano, Chie Hashimoto, et al.Pageof 8