| Literature DB >> 28935264 |
Naoki Nishizawa1, Yoko Kanematsu-Yamaki2, Masaaki Funata2, Hiroaki Nagai2, Ayako Shimizu2, Hisashi Fujita2, Junichi Sakamoto2, Shiro Takekawa2, Taiji Asami3.
Abstract
Neuromedin U (NMU) mediates various physiological functions via NMUR1 and NMUR2 receptors. NMUR2 has been considered a promising treatment option for diabetes and obesity. Although NMU-8, a shorter peptide, has potent agonist activity for both receptors, it is metabolically unstable. Therefore, NMU-8 analogs modified with long-chain alkyl moieties via a linker were synthesized. An octadecanoyl analog (17) with amino acid substitutions [αMePhe19, Nle21, and Arg(Me)24] and a linker [Tra-γGlu-PEG(2)] dramatically increased NMUR2 selectivity, with retention of high agonist activity. Subcutaneous administration of 17 induced anorectic activity in C57BL/6J mice. Owing to its high metabolic stability, 17 would be useful in clarifying the physiological role and therapeutic application of NMU.Entities:
Keywords: Diabetes; NMU-8; Neuromedin U (NMU); Obesity; Polyethylene glycol (PEG)
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Year: 2017 PMID: 28935264 DOI: 10.1016/j.bmcl.2017.09.019
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823