| Literature DB >> 29574204 |
Jiyu Jin1, Chunxiao Miao2, Zhilong Wang3, Wanli Zhang2, Xiongwen Zhang4, Xin Xie5, Wei Lu6.
Abstract
β-adrenergic receptors (β-ARs) are broadly distributed in various tissues and regulate a panel of important physiological functions and disease states including cancer. Above all, β3-adrenergic receptor (β3-AR) plays a significant role in regulating lipolysis and thermogenesis in adipose tissue. In this study, we designed and synthesized a series of novel L-748,337 derivatives as selective human β3-AR antagonists. Among all the tested L-748,337 analogs, compound 23d was found to display 23-fold more potent β3-AR antagonist activity (EC50 = 0.5117 nM) than L-748,337 (EC50 = 11.91 nM). In vivo, compound 23d could alleviate weight loss and inhibit tumor growth in C26 tumor cachexia animal model.Entities:
Keywords: Antagonist; Cancer; Lipolysis and cachexia; β-Adrenergic receptor
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Year: 2018 PMID: 29574204 DOI: 10.1016/j.ejmech.2018.03.032
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514