Cyclic Peptides in Pipeline: What Future for These Great Molecules?

被引:34
作者
Costa, Lia [1 ,2 ]
Sousa, Emilia [1 ,2 ]
Fernandes, Carla [1 ,2 ]
机构
[1] Univ Porto, Fac Farm, Dept Ciencias Quim, Lab Quim Organ & Farmaceut, Rua Jorge Viterbo Ferreira 228, P-4050313 Porto, Portugal
[2] Interdisciplinary Ctr Marine & Environm Res CIIMAR, EdifTerminal Cruzeiros Porto Leixoes, Ave Gen Nort, P-4050208 Matosinhos, Portugal
关键词
bioactivity; clinical trials; cyclic peptides; cyclization; pipeline; DECOMPENSATED HEART-FAILURE; ANTAGONIST PLUS ERIBULIN; RECENT PROGRESS; IN-VITRO; DOUBLE-BLIND; ENZYMATIC CYCLIZATION; STAUDINGER LIGATION; BIOACTIVE PEPTIDES; DRUG DISCOVERY; BROAD-SPECTRUM;
D O I
10.3390/ph16070996
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cyclic peptides are molecules that are already used as drugs in therapies approved for various pharmacological activities, for example, as antibiotics, antifungals, anticancer, and immunosuppressants. Interest in these molecules has been growing due to the improved pharmacokinetic and pharmacodynamic properties of the cyclic structure over linear peptides and by the evolution of chemical synthesis, computational, and in vitro methods. To date, 53 cyclic peptides have been approved by different regulatory authorities, and many others are in clinical trials for a wide diversity of conditions. In this review, the potential of cyclic peptides is presented, and general aspects of their synthesis and development are discussed. Furthermore, an overview of already approved cyclic peptides is also given, and the cyclic peptides in clinical trials are summarized.
引用
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页数:35
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共 261 条
  • [1] Single Dose of the CXCR4 Antagonist BL-8040 Induces Rapid Mobilization for the Collection of Human CD34+ Cells in Healthy Volunteers
    Abraham, Michal
    Pereg, Yaron
    Bulvik, Baruch
    Klein, Shiri
    Mishalian, Inbal
    Wald, Hana
    Eizenberg, Orly
    Beider, Katia
    Nagler, Arnon
    Golan, Rottem
    Vainstein, Abi
    Aharon, Arnon
    Galun, Eithan
    Caraco, Yoseph
    Or, Reuven
    Peled, Amnon
    [J]. CLINICAL CANCER RESEARCH, 2017, 23 (22) : 6790 - 6801
  • [2] CyClick Chemistry for the Synthesis of Cyclic Peptides
    Adebomi, Victor
    Cohen, Ryan D.
    Wills, Rachel
    Chavers, Holland Andrew Hays
    Martin, Gary E.
    Raj, Monika
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2019, 58 (52) : 19073 - 19080
  • [3] The Pharmacological Potential of Non-ribosomal Peptides from Marine Sponge and Tunicates
    Agrawal, Shivankar
    Adholeya, Alok
    Deshmukh, Sunil K.
    [J]. FRONTIERS IN PHARMACOLOGY, 2016, 7
  • [4] Echinocandins: The Expanding Antifungal Armamentarium
    Aguilar-Zapata, Daniel
    Petraitiene, Ruta
    Petraitis, Vidmantas
    [J]. CLINICAL INFECTIOUS DISEASES, 2015, 61 : S604 - S611
  • [5] Exploring Marine as a Rich Source of Bioactive Peptides: Challenges and Opportunities from Marine Pharmacology
    Ahmed, Ishtiaq
    Asgher, Muhammad
    Sher, Farooq
    Hussain, Syed Makhdoom
    Nazish, Nadia
    Joshi, Navneet
    Sharma, Ashutosh
    Parra-Saldivar, Roberto
    Bilal, Muhammad
    Iqbal, Hafiz M. N.
    [J]. MARINE DRUGS, 2022, 20 (03)
  • [6] aileronrx, OUR APPROACH PROTECT
  • [7] aileronrx, CLIN DEV
  • [8] Bioactive Peptides: Synthesis, Sources, Applications, and Proposed Mechanisms of Action
    Akbarian, Mohsen
    Khani, Ali
    Eghbalpour, Sara
    Uversky, Vladimir N.
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (03)
  • [9] Greening Fmoc/tBu solid-phase peptide synthesis
    Al Musaimi, Othman
    de la Torre, Beatriz G.
    Albericio, Fernando
    [J]. GREEN CHEMISTRY, 2020, 22 (04) : 996 - 1018
  • [10] Developments in peptide and amide synthesis
    Albericio, F
    [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 2004, 8 (03) : 211 - 221