GIP/GLP1 CO-AGONIST COMPOUNDS

To provide compounds that have agonist activity at both the human glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptors and are suitable for oral administration.SOLUTION: The present invention provides a compound having a specific amino acid sequence or a p...

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Hauptverfasser: QU HONGCHANG, JORGE ALSINA-FERNANDEZ, FRANCIS STAFFORD WILLARD, JAMES LINCOLN WALLIS, COSKUN TAMER, OVER CABRERA, ROBERT CHADWICK CUMMINS, AKTHAM ABURUB, KYLE WYNN SLOOP, ROBERT ANDREW BROWN, MOHAMED ELSAYED HAMED ELSAYED, MILATA MARY ABRAHAM, PHENIL JAYANTILAL PATEL, THI THANH HUYEN TRAN, AMITA DATTA-MANNAN, LAI XIANYIN
Format: Patent
Sprache:eng ; jpn
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Beschreibung
Zusammenfassung:To provide compounds that have agonist activity at both the human glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptors and are suitable for oral administration.SOLUTION: The present invention provides a compound having a specific amino acid sequence or a pharmaceutically acceptable salt thereof.SELECTED DRAWING: None 【課題】ヒトグルコース依存性インスリン分泌刺激ポリペプチド(GIP)受容体およびグルカゴン様ペプチド-1(GLP-1)受容体でアゴニスト活性を有する、経口投与に適した化合物を提供する。【解決手段】特定のアミノ酸配列を有する化合物、またはその薬学的に許容可能な塩による。【選択図】なし