Synthesis of Diphenylmethyl Analogues and Their Affinity for the Melanocortin-4 Receptor and the Serotonin Transporter
スポンサーリンク
概要
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While examining antagonists of the melanocortin-4 receptor (MC4 receptor), we found that compound 12b, containing a diphenylmethyl moiety, had a relatively high affinity for the MC4 receptor. When diphenylmethyl analogues were further examined, compounds 12c and 18 were also found to exhibit a high affinity for the MC4 receptor (IC_<50>=46.7nM and 33.2 nM, respectively). Furthermore, compound 12c was also found to show a high affinity for the serotonin transporter (IC_<50>=10.7 nM). Here, we describe the synthesis and biological evaluation of various diphenylmethyl analogues in relation to their actions on the MC4 receptor and the serotonin transporter.
- 2007-07-01
著者
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NAKAZATO Atsuro
Medicinal Research Laboratories, Taisho Pharmaceutical Co., Ltd.
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Chaki Shigeyuki
Medicinal Research Laboratories Taisho Pharmaceutical Co. Ltd.
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Chaki Shigeyuki
Medicinal Pharmacology Laboratory Taisho Pharmaceutical Co. Ltd.
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NOZAWA Dai
Medicinal Research Laboratories, Taisho Pharmaceutical Co., Ltd.
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OKUBO Taketoshi
Medicinal Research Laboratories, Taisho Pharmaceutical Co., Ltd.
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OKUYAMA Shigeru
Medicinal Research Laboratories, Taisho Pharmaceutical Co., Ltd.
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ISHII Takaaki
Medicinal Research Laboratories, Taisho Pharmaceutical Co., Ltd.
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Nakazato Atsuro
Medicinal Research Laboratories Taisho Pharmaceutical Co. Ltd.
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Okuyama Shigeru
Medicinal Research Laboratories Taisho Pharmaceutical Co. Ltd.
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Ishii Takaaki
Medicinal Research Laboratories Taisho Pharmaceutical Co. Ltd.
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Okubo Taketoshi
Medicinal Research Laboratories Taisho Pharmaceutical Co. Ltd.
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Nozawa Dai
Medicinal Research Laboratories Taisho Pharmaceutical Co. Ltd.
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Nakazato Atsuro
Strategic Planning Of Drug Discovery R&d Headquarters Of Pharmaceutical Operation Taisho Pharmaceutical Co. Ltd. Jpn
関連論文
- Identification of Arginine Analogues as Antagonists and Agonists for the Melanocortin-4 Receptor
- Synthesis of Diphenylmethyl Analogues and Their Affinity for the Melanocortin-4 Receptor and the Serotonin Transporter
- The Role of the DRY Motif of Human MC4R for Receptor Activation
- Scalable Synthesis of (+)-2-Amino-3-fluorobicyclo [3.1.0] hexane-2,6-dicarboxylic Acid as a Potent and Selective Group II Metabotropic Glutamate Receptor Agonist