Year |
Citation |
Score |
2022 |
Young HA, Proulx C. On-resin Cα-functionalization of -arylglycinyl peptides with boronic acids. Organic & Biomolecular Chemistry. PMID 35616496 DOI: 10.1039/d2ob00524g |
0.304 |
|
2020 |
Frégeau G, Sarduy R, Elimam H, Esposito CL, Mellal K, Ménard L, Leitão da Graça SD, Proulx C, Zhang J, Febbraio M, Soto Y, Lubell WD, Ong H, Marleau S. Atheroprotective and atheroregressive potential of azapeptide derivatives of GHRP-6 as selective CD36 ligands in apolipoprotein E-deficient mice. Atherosclerosis. 307: 52-62. PMID 32721647 DOI: 10.1016/J.Atherosclerosis.2020.06.010 |
0.561 |
|
2020 |
Proulx C, Zhang J, Sabatino D, Chemtob S, Ong H, Lubell WD. Synthesis and Biomedical Potential of Azapeptide Modulators of the Cluster of Differentiation 36 Receptor (CD36). Biomedicines. 8. PMID 32717955 DOI: 10.3390/Biomedicines8080241 |
0.54 |
|
2019 |
Guthrie QAE, Young HA, Proulx C. Ketoxime peptide ligations: oxidative couplings of alkoxyamines to -aryl peptides. Chemical Science. 10: 9506-9512. PMID 32110307 DOI: 10.1039/C9Sc04028E |
0.422 |
|
2019 |
Young HA, Guthrie QAE, Proulx C. N-Arylation of Amino Acid Esters to Expand Side Chain Diversity in Ketoxime Peptide Ligations. The Journal of Organic Chemistry. PMID 31793778 DOI: 10.1021/Acs.Joc.9B02810 |
0.414 |
|
2019 |
Reese HR, Shanahan CC, Proulx C, Menegatti S. Peptide science: a "rule model" for new generations of peptidomimetics. Acta Biomaterialia. PMID 31698048 DOI: 10.1016/J.Actbio.2019.10.045 |
0.437 |
|
2019 |
McMechen MA, Willis EL, Gourville PC, Proulx C. Aza-Amino Acids Disrupt β-Sheet Secondary Structures. Molecules (Basel, Switzerland). 24. PMID 31109055 DOI: 10.3390/Molecules24101919 |
0.369 |
|
2018 |
Guthrie QAE, Proulx C. Oxime Ligation via in situ Oxidation of N-Phenylglycinyl Peptides. Organic Letters. PMID 29694052 DOI: 10.1021/Acs.Orglett.8B00713 |
0.361 |
|
2018 |
Battigelli A, Kim JH, Dehigaspitiya DC, Proulx C, Robertson EJ, Murray DJ, Rad B, Kirshenbaum K, Zuckermann RN. Glycosylated Peptoid Nanosheets as a Multivalent Scaffold for Protein Recognition. Acs Nano. PMID 29512997 DOI: 10.1021/Acsnano.7B08018 |
0.658 |
|
2018 |
Frégeau G, Sarduy R, Ménard L, Machane S, Mahroug A, Proulx C, Lubell WD, Ong H, Marleau S. Athroprotective and Atheroregressive Potential of an [aza-Y4]-GHRP-6 Analogue, a Selective CD36 Ligand, in Apolipoprotein E-deficient Mice Atherosclerosis Supplements. 32: 160-161. DOI: 10.1016/J.Atherosclerosissup.2018.04.486 |
0.52 |
|
2017 |
Huynh DN, Bessi VL, Ménard L, Piquereau J, Proulx C, Febbraio M, Lubell WD, Carpentier AC, Burelle Y, Ong H, Marleau S. Adiponectin has a pivotal role in the cardioprotective effect of CP-3(iv), a selective CD36 azapeptide ligand, after transient coronary artery occlusion in mice. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. PMID 29018142 DOI: 10.1096/Fj.201700505R |
0.515 |
|
2017 |
Chingle R, Proulx C, Lubell WD. Azapeptide Synthesis Methods for Expanding Side-Chain Diversity for Biomedical Applications. Accounts of Chemical Research. PMID 28598597 DOI: 10.1021/Acs.Accounts.7B00114 |
0.637 |
|
2016 |
Robertson EJ, Proulx C, Su JK, Garcia RL, Yoo S, Nehls EM, Connolly MD, Taravati L, Zuckermann RN. Molecular Engineering of the Peptoid Nanosheet Hydrophobic Core. Langmuir : the Acs Journal of Surfaces and Colloids. PMID 27794618 DOI: 10.1021/Acs.Langmuir.6B02735 |
0.602 |
|
2016 |
Proulx C, Noë F, Yoo S, Connolly MD, Zuckermann RN. On-Resin N-Terminal Peptoid Degradation: Toward Mild Sequencing Conditions. Biopolymers. PMID 27258140 DOI: 10.1002/Bip.22884 |
0.585 |
|
2016 |
Flood D, Proulx C, Robertson EJ, Battigelli A, Wang S, Schwartzberg AM, Zuckermann RN. Improved chemical and mechanical stability of peptoid nanosheets by photo-crosslinking the hydrophobic core. Chemical Communications (Cambridge, England). PMID 26864502 DOI: 10.1039/C6Cc00588H |
0.535 |
|
2016 |
Robertson EJ, Battigelli A, Proulx C, Mannige RV, Haxton TK, Yun L, Whitelam S, Zuckermann RN. Design, Synthesis, Assembly, and Engineering of Peptoid Nanosheets. Accounts of Chemical Research. PMID 26741294 DOI: 10.1021/Acs.Accounts.5B00439 |
0.599 |
|
2015 |
Mannige RV, Haxton TK, Proulx C, Robertson EJ, Battigelli A, Butterfoss GL, Zuckermann RN, Whitelam S. Peptoid nanosheets exhibit a new secondary-structure motif. Nature. 526: 415-20. PMID 26444241 DOI: 10.1038/Nature15363 |
0.563 |
|
2015 |
Proulx C, Yoo S, Connolly MD, Zuckermann RN. Accelerated Submonomer Solid-Phase Synthesis of Peptoids Incorporating Multiple Substituted N-Aryl Glycine Monomers. The Journal of Organic Chemistry. PMID 26280152 DOI: 10.1021/Acs.Joc.5B01449 |
0.575 |
|
2014 |
Sanii B, Haxton TK, Olivier GK, Cho A, Barton B, Proulx C, Whitelam S, Zuckermann RN. Structure-determining step in the hierarchical assembly of peptoid nanosheets. Acs Nano. 8: 11674-84. PMID 25327498 DOI: 10.1021/Nn505007U |
0.702 |
|
2014 |
Robertson EJ, Oliver GK, Qian M, Proulx C, Zuckermann RN, Richmond GL. Assembly and molecular order of two-dimensional peptoid nanosheets through the oil-water interface. Proceedings of the National Academy of Sciences of the United States of America. 111: 13284-9. PMID 25197049 DOI: 10.1073/Pnas.1414843111 |
0.55 |
|
2014 |
Zhang J, Proulx C, Tomberg A, Lubell WD. Multicomponent diversity-oriented synthesis of aza-lysine-peptide mimics. Organic Letters. 16: 298-301. PMID 24328523 DOI: 10.1021/Ol403297V |
0.605 |
|
2014 |
Proulx C, Lubell WD. Analysis of N-amino-imidazolin-2-one peptide turn mimic 4-position substituent effects on conformation by X-ray crystallography. Biopolymers. 102: 7-15. PMID 23897495 DOI: 10.1002/Bip.22327 |
0.596 |
|
2014 |
Sun J, Proulx C, Zuckermann RN. Precision sequence control in bioinspired peptoid polymers Acs Symposium Series. 1170: 35-53. DOI: 10.1021/bk-2014-1170.ch003 |
0.456 |
|
2012 |
Proulx C, Lubell WD. N-Amino-imidazolin-2-one peptide mimic synthesis and conformational analysis. Organic Letters. 14: 4552-5. PMID 22892053 DOI: 10.1021/Ol302021N |
0.616 |
|
2012 |
Proulx C, Picard É, Boeglin D, Pohankova P, Chemtob S, Ong H, Lubell WD. Azapeptide analogues of the growth hormone releasing peptide 6 as cluster of differentiation 36 receptor ligands with reduced affinity for the growth hormone secretagogue receptor 1a. Journal of Medicinal Chemistry. 55: 6502-11. PMID 22712585 DOI: 10.1021/Jm300557T |
0.569 |
|
2011 |
Proulx C, Sabatino D, Hopewell R, Spiegel J, García Ramos Y, Lubell WD. Azapeptides and their therapeutic potential. Future Medicinal Chemistry. 3: 1139-64. PMID 21806378 DOI: 10.4155/Fmc.11.74 |
0.607 |
|
2011 |
Bolduc OR, Lambert-Lanteigne P, Colin DY, Zhao SS, Proulx C, Boeglin D, Lubell WD, Pelletier JN, Féthière J, Ong H, Masson JF. Modified peptide monolayer binding His-tagged biomolecules for small ligand screening with SPR biosensors. The Analyst. 136: 3142-8. PMID 21698315 DOI: 10.1039/C1An15235A |
0.611 |
|
2011 |
Sabatino D, Proulx C, Pohankova P, Ong H, Lubell WD. Structure-activity relationships of GHRP-6 azapeptide ligands of the CD36 scavenger receptor by solid-phase submonomer azapeptide synthesis. Journal of the American Chemical Society. 133: 12493-506. PMID 21692501 DOI: 10.1021/Ja203007U |
0.612 |
|
2010 |
Proulx C, Lubell WD. Aza-1,2,3-triazole-3-alanine synthesis via copper-catalyzed 1,3-dipolar cycloaddition on aza-progargylglycine. The Journal of Organic Chemistry. 75: 5385-7. PMID 20583744 DOI: 10.1021/Jo100957Z |
0.59 |
|
2010 |
Proulx C, Lubell WD. Copper-catalyzed N-arylation of semicarbazones for the synthesis of aza-arylglycine-containing aza-peptides. Organic Letters. 12: 2916-9. PMID 20536163 DOI: 10.1021/Ol100932M |
0.624 |
|
2010 |
Bourguet CB, Proulx C, Klocek S, Sabatino D, Lubell WD. Solution-phase submonomer diversification of aza-dipeptide building blocks and their application in aza-peptide and aza-DKP synthesis. Journal of Peptide Science : An Official Publication of the European Peptide Society. 16: 284-96. PMID 20474040 DOI: 10.1002/Psc.1235 |
0.59 |
|
2009 |
Sabatino D, Proulx C, Klocek S, Bourguet CB, Boeglin D, Ong H, Lubell WD. Exploring side-chain diversity by submonomer solid-phase aza-peptide synthesis. Organic Letters. 11: 3650-3. PMID 19606817 DOI: 10.1021/Ol901423C |
0.618 |
|
2009 |
Bourguet CB, Dörr A, Godina T, Proulx C, Fridkin G, Jamieson A, Sabatino D, Kassem T, Boutard N, Arsenault J, Ronga L, Brouillette Y, Bednarek M, Tolles JC, Lubell WD. Portraits of the pioneers of the American Peptide Society. Advances in Experimental Medicine and Biology. 611: xlix-lxix. PMID 19400064 |
0.498 |
|
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