Invention Grant
- Patent Title: Developing potent urate transporter inhibitors: compounds designed for their uricosuric action
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Application No.: US13823522Application Date: 2011-10-06
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Publication No.: US10005750B2Publication Date: 2018-06-26
- Inventor: Michael F. Wempe , Hitoshi Endou
- Applicant: Michael F. Wempe , Hitoshi Endou
- Applicant Address: JP Tokyo
- Assignee: J-Pharma Co., Ltd.
- Current Assignee: J-Pharma Co., Ltd.
- Current Assignee Address: JP Tokyo
- Agency: Osha Liang LLP
- International Application: PCT/US2011/055006 WO 20111006
- International Announcement: WO2012/048058 WO 20120412
- Main IPC: C07D307/84
- IPC: C07D307/84 ; C07D209/12 ; C07D307/79 ; C07D307/80

Abstract:
A compound represented by the general Formula I: a pharmaceutically acceptable salt or ester thereof, a solvate thereof, a chelate thereof, a non-covalent complex thereof, a pro-drug thereof, a deuterated radio-labeled analog thereof, and mixtures of any of the foregoing, wherein: A-K are individually selected from carbon or nitrogen; X═—O, —NR1, or —S; R1-11 are individually selected from the group consisting of —H, C1-C6 alkyl, C6-C14 aryl, substituted C6-C14 aryl, C1-C14-alkoxy, halogen, hydroxyl, carboxy, cyano, C1-C6-alkanoyloxy, C1-C6-alkylthio, C1-C6-alkylsulfonyl, trifluoromethyl, hydroxy, C2-C6-alkoxycarbonyl, C2-C6-alkanoylamino, —O—R12, S—R12, —SO2—R12, —NHSO2R12 and —NHCO2R12, wherein R12 is phenyl, naphthyl, or phenyl or naphthly substituted with one to three groups selected from C1-C6-alkyl, C6-C10 aryl, C1-C6-alkoxy and halogen, and C4-C20 hydroxyheteroaryl wherein the heteroatoms are selected from the group consisting of sulfur, nitrogen, and oxygen.
Public/Granted literature
- US20130225673A1 DEVELOPING POTENT URATE TRANSPORTER INHIBITORS: COMPOUNDS DESIGNED FOR THEIR URICOSURIC ACTION Public/Granted day:2013-08-29
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