A Robust Platform for the Molecular Design of Potent, Protease-Stable, Long-Acting GIP Analogues-Reference-Cited by-同舟云学术

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A Robust Platform for the Molecular Design of Potent, Protease-Stable, Long-Acting GIP Analogues

Published:2024-03-08 Issue:6 Volume:67 Page:4998-5010
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Sicinski Kathleen M.¹,Sürmeli Damla¹^ORCID,Du Jasper¹,Raman Venkata S.¹,Montanari Vittorio¹,Lee Minhee¹,Harwood Benjamin N.²,Kopin Alan S.²,Beinborn Martin¹³,Kumar Krishna¹^ORCID

Affiliation:

1. Department of Chemistry, Tufts University, Medford, Massachusetts 02155, United States

2. Molecular Cardiology Research Institute, Tufts Medical Center, Boston, Massachusetts 02111, United States

3. Molecular Pharmacology Research Center, Tufts Medical Center, Boston, Massachusetts 02111, United States

Funder

Tufts Medical Center

Division of Diabetes, Endocrinology, and Metabolic Diseases

National Institute on Aging

Tufts University

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jmedchem.4c00111

Reference55 articles.

1. The expanding incretin universe: from basic biology to clinical translation

2. The biology of incretin hormones

3. International Union of Pharmacology. XXXV. The Glucagon Receptor Family

4. Separate and Combined Glucometabolic Effects of Endogenous Glucose-Dependent Insulinotropic Polypeptide and Glucagon-like Peptide 1 in Healthy Individuals

5. GIP and GLP-1: Stepsiblings Rather Than Monozygotic Twins Within the Incretin Family

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