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      1. Home
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      3. CPC Scientific

      CPC_Scientific Archive

      • Fatty acid derivatization and cyclization of the immunomodulatory peptide RP-182 targeting CD206high macrophages improves anti-tumor activity

        Singh, S.S., Calvo, R., Kumari, A., Sable, R.V., Fang, Y., Tao, D., Hu, X., Castle, S.G., Nahar, S., Li, D. and Major, E. Molecular Cancer Therapeutics (2024).

        • CPC Scientific Inc., 160E Tasman Dr., Suite 200, San Jose, CA 95134

        [..] assembling the peptide on the Rink Amide resin and attaching the PEG azide moiety to the N-terminal Lys, the Dde group was removed as previously shown and coupled to the Fmoc-PEG2-acid. Removal of the Fmoc followed by simultaneously click/coupling to bicyclo[6.1.0]non-4-yn-9-ylmethyl (2,5-dioxopyrrolidin-1-yl) carbonate gave 1c which was deprotected and cleaved from the resin to give 1c.

        Published On: August 30th, 2024Categories: Citations, Click Peptides, coauthored, Green Chemistry, PEGylation, Peptide Macrocycles, publications, Stapled Peptides
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      • A Non-immunogenic Bivalent D-Protein Potently Inhibits Retinal Vascularization and Tumor Growth

        Paul S. Marinec, Kyle E. Landgraf, Maruti Uppalapati, Gang Chen, Daniel Xie,‡ Qiyang Jiang, Yanlong Zhao, Annalise Petriello, Kurt Deshayes, Stephen B. H. Kent, Dana Ault-Riche*, and Sachdev S. Sidhu* ACS Chem. Biol. 2021, 16, 3, 548–556.

        • Chinese Peptide Company, Hangzhou Economic and Technical Development Zone, China, 310018.

        "The D-VEGF-A polypeptide chain (COOH acid, residues 8-109 (1)) was chemically synthesized using solid phase peptide synthesis (SPPS) and native chemical ligation, and folded to form the protein covalent homodimer, using methods adapted from our previous work [..]"

        Published On: March 19th, 2021Categories: Citations, Click Peptides, coauthored, PEGylation, publications
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      • Discovery of Dap‑3 Polymyxin Analogues for the Treatment of Multidrug-Resistant Gram-Negative Nosocomial Infections.

        Magee, T.V., Brown, M.F., Starr, J.T., Ackley, D.C., Abramite, J.A., Aubrecht, J., Butler, A., Crandon, J.L., Dib-Hajj, F., Flanagan, M.E. and Granskog, K. Journal of Medicinal Chemistry 56, no. 12 (2013): 5079-5093.

        1. Pfizer Worldwide Research & Development, Pfizer, Inc., Groton, Connecticut 06340, United States
        2. CPC Scientific, Hangzhou, P.R. China
        Published On: June 4th, 2013Categories: Citations, coauthored, Peptide Macrocycles, publications, Unnatural Amino Acids
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      • Design and structure of stapled peptides binding to estrogen receptors.

        Phillips, Chris, et al. Journal of the American Chemical Society 133.25 (2011): 9696-9699.

        "Synthetic peptides that specifically bind nuclear hormone receptors offer an alternative approach to small molecules for the modulation of receptor signaling and subsequent gene expression. [..] Using a number of biophysical techniques, including crystal structure analysis of receptor–stapled peptide complexes, we describe in detail the molecular interactions and demonstrate that all-hydrocarbon staples modulate molecular recognition events."

        Published On: May 25th, 2011Categories: Citations, coauthored, publications, Stapled Peptides
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