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Chemmedchem|October 26, 2016
Retro-1 Analogues Differentially Affect Oligonucleotide Delivery and Toxin TraffickingBing Yang, Xin Ming, Hajer Abdelkafi, et al.
Chemmedchem|October 28, 2016
Introducing Glycolinkers for the Functionalization of Cytotoxic Drugs and Applications in Antibody-Drug Conjugation ChemistryFilip S Ekholm, Henna Pynnönen, Anja Vilkman, et al.
Chemmedchem|October 28, 2016
Targeting Cancer Cells with a Bisphosphonate ProdrugKenji Matsumoto, Kosuke Hayashi, Kaoru Murata-Hirai, et al.
Chemmedchem|January 4, 2017
Preparation of a Salecan/poly(2-acrylamido-2-methylpropanosulfonic acid-co-[2-(methacryloxy)ethyl]trimethylammonium chloride) Semi-IPN Hydrogel for Drug DeliveryXiaoliang Qi, Junjian Li, Wei Wei, et al.
Chemmedchem|December 20, 2016
Inhibition of the Cysteine Protease Human Cathepsin L by Triazine Nitriles: Amide⋅⋅⋅Heteroarene π-Stacking Interactions and Chalcogen Bonding in the S3 PocketMaude Giroud, Jakov Ivkovic, Mara Martignoni, et al.
Chemmedchem|December 25, 2007
Synthesis, biological evaluation, and molecular modeling studies of rebeccamycin analogues modified in the carbohydrate moietyFabio Animati, Marco Berettoni, Mario Bigioni, et al.
Chemmedchem|December 25, 2007
Reduction of lipophilicity at the lipophilic domain of RXR agonists enables production of subtype preference: RXRalpha-preferential agonist possessing a sulfonamide moietyKayo Takamatsu, Atsushi Takano, Nobumasa Yakushiji, et al.
Chemmedchem|February 6, 2008
Synthesis and biological evaluation of isosteric analogues of FK866, an inhibitor of NAD salvageUbaldina Galli, Emanuela Ercolano, Lorenzo Carraro, et al.
Chemmedchem|January 5, 2008
Identification of putative binding sites of P-glycoprotein based on its homology modelChristoph Globisch, Ilza K Pajeva, Michael Wiese
Chemmedchem|February 6, 2014
Bromodomains and their pharmacological inhibitorsDaniel Gallenkamp, Kathy A Gelato, Bernard Haendler, et al.
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