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10.1002/chem.201504936 http://scihub22266oqcxt.onion/10.1002/chem.201504936 C4955406!4955406!26945679     free     free     free       Chemistry 2016 ; 22 (16): 5458-66 Nephropedia Template TP {{tp|p=26945679|t=2016. ?-AApeptides as a new class of peptidomimetics |pdf=|usr=}}{{26945679}} gab.com Text -AApeptides as a new class of peptidomimetics JO: Chemistry http://www.kidney.de/pget.php?&tw=1&pmid=26945679 #FOAvip Sequence-specific peptidomimetics are molecules that mimic structure and function of peptides and proteins. With new backbones and molecular frameworks, peptidomimetics are of considerable interest to address challenges encountered in chemical biology and biomedical sciences. Based on the ?-PNA backbone, a new class of peptidomimetics - "?-AApeptides" were recently developed. Both linear and cyclic ?-AApeptides can be synthesized with high efficiency. Compared with ?-peptides, ?-AApeptides are resistant to enzymatic degradation, and amendable to diversification with a variety of chemical groups. Moreover, they could mimic primary and secondary structure, as well as function of peptides, and show promise in biological applications, such as development of new agents combating bacteria, cancer, and Alzheimer?s disease (AD). A few research outcomes of ?-AApeptides are highlighted in this concept article, and a future perspective is also proposed. Twit Text FOAVip -AApeptides as a new class of peptidomimetics ????Chemistry http://www.kidney.de/pget.php?&tw=1&pmid=26945679 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26945679 #FOAvip English Wikipedia <ref>{{Cite pmid|26945679}}</ref> ?-AApeptides as a new class of peptidomimetics #MMPMID26945679 Teng P; Shi Y; Sang P; Cai J Chemistry 2016[Apr]; 22 (16): 5458-66 PMID26945679show ga Sequence-specific peptidomimetics are molecules that mimic structure and function of peptides and proteins. With new backbones and molecular frameworks, peptidomimetics are of considerable interest to address challenges encountered in chemical biology and biomedical sciences. Based on the ?-PNA backbone, a new class of peptidomimetics - "?-AApeptides" were recently developed. Both linear and cyclic ?-AApeptides can be synthesized with high efficiency. Compared with ?-peptides, ?-AApeptides are resistant to enzymatic degradation, and amendable to diversification with a variety of chemical groups. Moreover, they could mimic primary and secondary structure, as well as function of peptides, and show promise in biological applications, such as development of new agents combating bacteria, cancer, and Alzheimer?s disease (AD). A few research outcomes of ?-AApeptides are highlighted in this concept article, and a future perspective is also proposed. ä?-AApeptides as a new class of peptidomimetics (epmc).pdf DeepDyve Pubget Overpricing