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Review ArticleReview Article

Novel Pharmacological Approaches to the Treatment of Type 2 Diabetes

E. J. Verspohl
Martin C. Michel, ASSOCIATE EDITOR
Pharmacological Reviews April 2012, 64 (2) 188-237; DOI: https://doi.org/10.1124/pr.110.003319
E. J. Verspohl
Institute for Pharmaceutical Sciences, Department Pharmacology, University of Muenster, Muenster, Germany
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Martin C. Michel
Institute for Pharmaceutical Sciences, Department Pharmacology, University of Muenster, Muenster, Germany
Roles: ASSOCIATE EDITOR
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Article Information

vol. 64 no. 2 188-237
DOI 
https://doi.org/10.1124/pr.110.003319
PubMed 
22407617

Published By 
American Society for Pharmacology and Experimental Therapeutics
Print ISSN 
0031-6997
Online ISSN 
1521-0081
History 
  • Published online March 14, 2012.

Article Versions

  • Earlier version (March 8, 2012 - 05:54).
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© 2012 by The American Society for Pharmacology and Experimental Therapeutics

Author Information

  1. E. J. Verspohl
  1. Institute for Pharmaceutical Sciences, Department Pharmacology, University of Muenster, Muenster, Germany
  1. Martin C. Michel, ASSOCIATE EDITOR
  1. Address correspondence to:
    Dr. Eugen J. Verspohl, Department of Pharmacology, Institute of Medicinal Chemistry, University of Muenster, Hittorfstr. 58-62, 48149 Muenster, Germany. E-mail: verspoh{at}uni-muenster.de
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Pharmacological Reviews: 64 (2)
Pharmacological Reviews
Vol. 64, Issue 2
1 Apr 2012
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Review ArticleReview Article

FUTURE TYPE 2 DIABETES THERAPY

E. J. Verspohl
Pharmacological Reviews April 1, 2012, 64 (2) 188-237; DOI: https://doi.org/10.1124/pr.110.003319

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Review ArticleReview Article

FUTURE TYPE 2 DIABETES THERAPY

E. J. Verspohl
Pharmacological Reviews April 1, 2012, 64 (2) 188-237; DOI: https://doi.org/10.1124/pr.110.003319
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  • Article
    • Abstract
    • I. Introduction
    • II. Incretin Mimetics and Incretin Analogs
    • III. Dipeptidyl-Peptidase 4 Inhibitors
    • IV. Sodium-Coupled Glucose Cotransporter 2 Inhibitors
    • V. Pramlintide (Amyloid Deposits, Amylin)
    • VI. Peroxisome Proliferator-Activated Receptor Agonists (New Glitazones and Glitazars); Glitazars Are Dual Peroxisome Proliferator-Activated Receptor Agonists
    • VII. New Glinides
    • VIII. Enzymes as Targets (Signaling Systems)
    • IX. Physiological Compounds (Hormones)
    • X. New Remedies with Respect to Late Complications of Diabetes
    • XI. G-Protein-Coupled Receptors
    • XII. Hypothetical New Targets (Emerging Targets) Still Lacking Therapeutic Significance
    • Acknowledgments
    • Authorship Contributions
    • Footnotes
    • References
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