Syntheses of isotope-labeled SGLT2 inhibitor canagliflozin (JNJ-28431754)

被引:1
|
作者
Lin, Ronghui [1 ]
Hoerr, David C. [1 ]
Weaner, Larry E. [1 ]
Salter, Rhys [1 ]
机构
[1] Janssen Pharmaceut Co Johnson & Johnson, Janssen Res & Dev LLC, Welsh & McKean Rd, Spring House, PA 19477 USA
关键词
canagliflozin; isotope label; SGLT2; inhibitor; synthesis; COTRANSPORTER; 2; INHIBITOR; TYPE-2; DIABETES-MELLITUS; GLUCOSE;
D O I
10.1002/jlcr.3542
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Canagliflozin (Invokana, JNJ-28431754) is an orally bioavailable and selective SGLT2 (subtype 2 sodium-glucose transport protein) inhibitor approved for the treatment of type 2 diabetes. Herein, we report the synthesis of C-13 and C-14-labeled canagliflozin. Stable isotope-labeled [C-13(6)]canagliflozin was synthesized in 4 steps starting from [C-13(6)]-labeled glucose. The [C-14]-Labeled canagliflozin was synthesized by incorporation of [C-14] into the benzylic position between the thiophene and benzene rings of the compound. Detailed synthesis of the isotope-labeled compounds is reported.
引用
收藏
页码:616 / 623
页数:8
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