Synthesis and SAR studies of a novel class of S1P1 receptor antagonists |
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Authors: | Nakamura Tsuyoshi Yonesu Kiyoaki Mizuno Yumiko Suzuki Chie Sakata Yuki Takuwa Yoh Nara Futoshi Satoh Susumu |
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Institution: | Medicinal Chemistry Research Laboratories, Sankyo Co., Ltd, 1-2-58 Hiromachi, Tokyo 140-8710, Japan. |
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Abstract: | A series of Sodium 4-(4-butoxyphenyl)thio]-2'-substituted-1,1'-biphenyl-3- sulfonates were identified as functional sphingosine-1-phosphate (S1P) antagonists with selectivity for the S1P(1) receptor subtype starting from chemical lead 2, which was found while screening our in-house compound library. We performed chemical modifications on each regional structure of compound 2, for example, on the three ring compartments, the benzyl substituents, and the long alkyl chain part. The introduction of a biphenyl skeletal structure and the installation of a hydroxyl group onto the terminal carbon in the side-chain region resulted in the potent derivative 35c, which showed >500-fold more potent S1P(1) inhibitory activity than lead compound 2. We report herein the synthesis and structure-activity relationships of structurally novel S1P(1) receptor antagonists. |
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