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Nats 1740 Assignment 231

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  • Chimeric RNA Oligonucleotides Incorporating Triazole-Linked Trinucleotides: Synthesis and Function as mRNA in Cell-Free Translation Reactions


    The Journal of Organic Chemistry201681 (19), 8967-8976

    Abstract | Full Text HTML | PDF | PDF w/ Links

  • Selective Amidation of Unprotected Amino Alcohols Using Surfactant-in-Water Technology: A Highly Desirable Alternative to Reprotoxic Polar Aprotic Solvents

    MichaelParmentierMona K.WagnerKevinMagraFabriceGallou

    Organic Process Research & Development201620 (6), 1104-1107

    Abstract | Full Text HTML | PDF | PDF w/ Links

  • Chimeric Agents Derived from the Functionalized Amino Acid, Lacosamide, and the α-Aminoamide, Safinamide: Evaluation of Their Inhibitory Actions on Voltage-Gated Sodium Channels, and Antiseizure and Antinociception Activities and Comparison with Lacosamide and Safinamide

    Ki DukParkXiao-FangYangErik T.DustrudeYuyingWangMatthew S.RipschFletcher A.WhiteRajeshKhannaHaroldKohn

    ACS Chemical Neuroscience20156 (2), 316-330

    Abstract | Full Text HTML | PDF | PDF w/ Links

  • Substituted N-(Biphenyl-4′-yl)methyl (R)-2-Acetamido-3-methoxypropionamides: Potent Anticonvulsants That Affect Frequency (Use) Dependence and Slow Inactivation of Sodium Channels

    HyosungLeeKi DukParkRobertTorregrosaXiao-FangYangErik T.DustrudeYuyingWangSarah M.WilsonCindyBarbosaYuchengXiaoTheodore R.CumminsRajeshKhannaHaroldKohn

    Journal of Medicinal Chemistry201457 (14), 6165-6182

    Abstract | Full Text HTML | PDF | PDF w/ Links

  • Discovery of Lacosamide Affinity Bait Agents That Exhibit Potent Voltage-Gated Sodium Channel Blocking Properties

    Ki DukParkXiao-FangYangHyosungLeeErik T.DustrudeYuyingWangRajeshKhannaHaroldKohn

    ACS Chemical Neuroscience20134 (3), 463-474

    Abstract | Full Text HTML | PDF | PDF w/ Links

  • Peptide Coupling Reagents, More than a Letter Soup


    Chemical Reviews2011111 (11), 6557-6602

    Abstract | Full Text HTML | PDF | PDF w/ Links

  • Defining the Structural Parameters That Confer Anticonvulsant Activity by the Site-by-Site Modification of (R)-N′-Benzyl 2-Amino-3-methylbutanamide

    Amber M.KingMarcDe RyckRafalKaminskiAnneValadeJames P.StablesHaroldKohn

    Journal of Medicinal Chemistry201154 (19), 6432-6442

    Abstract | Full Text HTML | PDF | PDF w/ Links

  • Primary Amino Acid Derivatives: Substitution of the 4′-N′-Benzylamide Site in (R)-N′-Benzyl 2-Amino-3-methylbutanamide, (R)-N′-Benzyl 2-Amino-3,3-dimethylbutanamide, and (R)-N′-Benzyl 2-Amino-3-methoxypropionamide Provides Potent Anticonvulsants with Pain-Attenuating Properties

    Amber M.KingChristopheSaloméEliseSalomé-GrosjeanMarcDe RyckRafalKaminskiAnneValadeJames P.StablesHaroldKohn

    Journal of Medicinal Chemistry201154 (19), 6417-6431

    Abstract | Full Text HTML | PDF | PDF w/ Links

  • Primary Amino Acid Derivatives: Compounds with Anticonvulsant and Neuropathic Pain Protection Activities

    Amber M.KingChristopheSaloméJasonDinsmore

  • 1. Wang M, Abbineni G, Clevenger A, Mao C, Xu S. Nanomedicine: NBM. 2011;7:710–729. doi: 10.1016/j.nano.2011.02.013.[PMC free article][PubMed][Cross Ref]

    2. Mader H S, Kele P, Saleh S M, Wolfbeis O S. Curr Opin Chem Biol. 2010;14:582–596. doi: 10.1016/j.cbpa.2010.08.014.[PubMed][Cross Ref]

    3. Liu C, Gao Z, Zeng J, Hou Y, Fang F, Li Y, Qiao R, Shen L, Lei H, Yang W, et al. ACS Nano. 2013;7:7227–7240. doi: 10.1021/nn4030898.[PubMed][Cross Ref]

    4. Deng R, Qin F, Chen R, Huang W, Hong M, Liu X. Nat Nanotechnol. 2015;10:237–242. doi: 10.1038/nnano.2014.317.[PubMed][Cross Ref]

    5. Sun Y, Feng W, Yang P, Huang C, Li F. Chem Soc Rev. 2015;44:1509–1525. doi: 10.1039/C4CS00175C.[PubMed][Cross Ref]

    6. Zhou J, Liu Z, Li F. Chem Soc Rev. 2012;41:1323–1349. doi: 10.1039/C1CS15187H.[PubMed][Cross Ref]

    7. Wang F, Banerjee D, Liu Y, Chen X, Liu X. Analyst. 2010;135:1839–1854. doi: 10.1039/c0an00144a.[PubMed][Cross Ref]

    8. Wang F, Liu X. Chem Soc Rev. 2009;38:976–989. doi: 10.1039/b809132n.[PubMed][Cross Ref]

    9. Guanying C, Gang H. Theranostics. 2013;3:289–291. doi: 10.7150/thno.6382.[PMC free article][PubMed][Cross Ref]

    10. Qiu H, Yang C, Shao W, Damasco J, Wang X, Ågren H, Prasad P N, Chen G. Nanomaterials. 2014;4:55. doi: 10.3390/nano4010055.[PMC free article][PubMed][Cross Ref]

    11. Liu Y, Tu D, Zhu H, Li R, Luo W, Chen X. Adv Mater. 2010;22:3266. doi: 10.1002/adma.201000128.[PubMed][Cross Ref]

    12. Wang F, Wang J, Liu X. Angew Chem. 2010;49:7456. doi: 10.1002/anie.201003959.[PubMed][Cross Ref]

    13. Chen D, Lei L, Yang A, Wang Z, Wang Y. Chem Commun. 2012;48:5898–5900. doi: 10.1039/c2cc32102e.[PubMed][Cross Ref]

    14. Liu F, He X, Liu L, You H, Zhang H, Wang Z. Biomaterials. 2013;34:5218–5225. doi: 10.1016/j.biomaterials.2013.03.058.[PubMed][Cross Ref]

    15. Cao T, Yang T, Gao Y, Yang Y, Hu H, Li F. Inorg Chem Commun. 2010;13:392–394. doi: 10.1016/j.inoche.2009.12.031.[Cross Ref]

    16. Chen Z, Chen H, Hu H, Yu M, Li F, Zhang Q, Zhou Z, Yi T, Huang C. J Am Chem Soc. 2008;130:3023–3029. doi: 10.1021/ja076151k.[PubMed][Cross Ref]

    17. Bogdan N, Vetrone F, Ozin G A, Capobianco J A. Nano Lett. 2011;11:835–840. doi: 10.1021/nl1041929.[PubMed][Cross Ref]

    18. Cheng L, Yang K, Zhang S, Shao M, Lee S, Liu Z. Nano Res. 2010;3:722–732. doi: 10.1007/s12274-010-0036-2.[Cross Ref]

    19. Zhao Y, Wang Z, Zhang W, Jiang X. Nanoscale. 2010;2:2114–2119. doi: 10.1039/c0nr00309c.[PubMed][Cross Ref]

    20. Huang Y, Zhang B, Xi S, Yang B, Xu Q, Tan J. ACS Appl Mater Interfaces. 2016;8:11336–11341. doi: 10.1021/acsami.6b02838.[PubMed][Cross Ref]

    21. Baalousha M, Arkill K P, Romer I, Palmer R E, Lead J R. Sci Total Environ. 2015;502:344–353. doi: 10.1016/j.scitotenv.2014.09.035.[PubMed][Cross Ref]

    22. Cascales C, Paíno C L, Bazán E, Zaldo C. Nanotechnology. 2017;28:185101. doi: 10.1088/1361-6528/aa6834.[PubMed][Cross Ref]

    23. Rogosnitzky M, Branch S. BioMetals. 2016;29:365–376. doi: 10.1007/s10534-016-9931-7.[PMC free article][PubMed][Cross Ref]

    24. Swaminathan S. Magn Reson Imaging. 2016;34:1373–1376. doi: 10.1016/j.mri.2016.08.016.[PubMed][Cross Ref]

    25. Park S, Mohanty N, Suk J W, Nagaraja A, An J, Piner R D, Cai W, Dreyer D R, Berry V, Ruoff R S. Adv Mater. 2010;22:1736–1740. doi: 10.1002/adma.200903611.[PubMed][Cross Ref]

    26. Yi G-S, Chow G-M. Chem Mater. 2007;19:341. doi: 10.1021/cm062447y.[Cross Ref]

    27. Wong H-T, Vetrone F, Naccache R, Chan H L W, Hao J, Capobianco J A. J Mater Chem. 2011;21:16589. doi: 10.1039/c1jm12796a.[Cross Ref]

    28. Baziulyte D, Karabanovas V, Stalnionis M, Jurciukonis I, Sakirzanovas S. Book of abstracts of the “Chemistry and Chemical Technology; International Conference of Lithuanian Society of Chemistry; 2016. p. 150.

    29. Johnson N J J, Oakden W, Stanisz G J, Scott Prosser R, van Veggel F C J M. Chem Mater. 2011;23:3714–3722. doi: 10.1021/cm201297x.[Cross Ref]

    30. Hou Y, Qiao R, Fang F, Wang X, Dong C, Liu K, Liu C, Liu Z, Lei H, Wang F, et al. ACS Nano. 2013;7:330–338. doi: 10.1021/nn304837c.[PubMed][Cross Ref]

    31. Vetrone F, Naccache R, de la Fuente A J, Sanz-Rodriguez F, Blazquez-Castro A, Rodriguez E M, Jaque D, Solé J G, Capobianco J A. Nanoscale. 2010;2:495–498. doi: 10.1039/B9NR00236G.[PubMed][Cross Ref]

    32. Karabanovas V, Zitkus Z, Kuciauskas D, Rotomskis R, Valius M. J Biomed Nanotechnol. 2014;10:775–786. doi: 10.1166/jbn.2014.1770.[PubMed][Cross Ref]

    33. Osman O, Zanini L F, Frénéa-Robin M, Dumas-Bouchiat F, Dempsey N M, Reyne G, Buret F, Haddour N. Biomed Microdevices. 2012;14:947–954. doi: 10.1007/s10544-012-9673-4.[PubMed][Cross Ref]

    34. Wang S-H, Lee C-W, Chiou A, Wei P-K. J Nanobiotechnol. 2010;8:33. doi: 10.1186/1477-3155-8-33.[PMC free article][PubMed][Cross Ref]

    35. Woźniak A, Noculak A, Gapiński J, Kociolek D, Boś-Liedke A, Zalewski T, Grześkowiak B F, Kołodziejczak A, Jurga S, Banski M, et al. RSC Adv. 2016;6:95633–95643. doi: 10.1039/C6RA20415E.[Cross Ref]

    36. Guller A E, Generalova A N, Petersen E V, Nechaev A V, Trusova I A, Landyshev N N, Nadort A, Grebenik E A, Deyev S M, Shekhter A B, et al. Nano Res. 2015;8:1546–1562. doi: 10.1007/s12274-014-0641-6.[Cross Ref]

    37. Ren W, Tian G, Jian S, Gu Z, Zhou L, Yan L, Jin S, Yin W, Zhao Y. RSC Adv. 2012;2:7037–7041. doi: 10.1039/c2ra20855e.[Cross Ref]

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