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      Discovery of Amantamide, a Selective CXCR7 Agonist from Marine Cyanobacteria

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          Abstract

          CXCR7 plays an emerging role in several physiological processes. A linear peptide, amantamide ( 1 ), was isolated from marine cyanobacteria and the structure determined by NMR and mass spectrometry. The total synthesis was achieved by solid-phase method. After screening two biological target libraries, 1 was identified as a selective CXCR7 agonist. The selective activation of CXCR7 by 1 could provide the basis for developing CXCR7 targeted therapeutics and deciphering the role of CXCR7 in different diseases.

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          Author and article information

          Journal
          Organic Letters
          Org. Lett.
          American Chemical Society (ACS)
          1523-7060
          1523-7052
          February 19 2019
          February 19 2019
          Affiliations
          [1 ]Department of Medicinal Chemistry and Center for Natural Products, Drug Discovery and Development (CNPD3), University of Florida, Gainesville, Florida 32610, United States
          [2 ]State Key Laboratory of Chemical Oncogenomics, Key Laboratory of Chemical Genomics, Peking University Shenzhen Graduate School, Xili, Nanshan District, Shenzhen 518055, China
          [3 ]Department of Chemistry, University of Florida, Gainesville, Florida 32611, United States
          [4 ]Marine Science Institute, College of Science, University of the Philippines, Diliman, Quezon City 1101, Philippines
          [5 ]Smithsonian Marine Station, Fort Pierce, Florida 34949, United States
          [6 ]QianYan Pharmatech Limited, Shenzhen, 518172, China
          Article
          10.1021/acs.orglett.9b00163
          7327960
          30779584
          8b5a9ff3-0205-46dc-b0d1-691f5cf09770
          © 2019
          History

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