| Literature DB >> 24900773 |
Sumihiro Nomura1, Yasuo Yamamoto1, Yosuke Matsumura1, Kiyomi Ohba1, Shigeki Sakamaki1, Hirotaka Kimata1, Keiko Nakayama1, Chiaki Kuriyama1, Yasuaki Matsushita1, Kiichiro Ueta1, Minoru Tsuda-Tsukimoto1.
Abstract
Inhibition of the renal sodium glucose cotransporter (SGLT) increases urinary glucose excretion (UGE) and thus reduces blood glucose levels during hyperglycemia. To explore the potential of new antihyperglycemic agents, we synthesized and determined the human SGLT2 (hSGLT2) inhibitory potential of novel substituted 3-benzylindole-N-glucosides 6. Optimization of 6 resulted in the discovery of 3-(4-cyclopropylbenzyl)-4-fluoroindole-N-glucoside 6a-4 (TA-1887), a highly potent and selective hSGLT2 inhibitor, with pronounced antihyperglycemic effects in high-fat diet-fed KK (HF-KK) mice. Our results suggest the potential of indole-N-glucosides as novel antihyperglycemic agents through inhibition of renal SGLT2.Entities:
Keywords: TA-1887; Type 2 diabetes; antihyperglycemic effect; indole-N-glucoside; sodium glucose cotransporter 2 inhibitor; urinary glucose excretion
Year: 2013 PMID: 24900773 PMCID: PMC4027614 DOI: 10.1021/ml400339b
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345