367501-39-1Relevant articles and documents
Discovery of DS-6930, a potent selective PPARγ modulator. Part I: Lead identification
Shinozuka, Tsuyoshi,Tsukada, Tomoharu,Fujii, Kunihiko,Tokumaru, Eri,Shimada, Kousei,Onishi, Yoshiyuki,Matsui, Yumi,Wakimoto, Satoko,Kuroha, Masanori,Ogata, Tsuneaki,Araki, Kazushi,Ohsumi, Jun,Sawamura, Ryoko,Watanabe, Nobuaki,Yamamoto, Hideki,Fujimoto, Kazunori,Tani, Yoshiro,Mori, Makoto,Tanaka, Jun
, p. 5079 - 5098 (2018/09/27)
The lead identification of a novel potent selective PPARγ agonist, DS-6930 is reported. To avoid PPARγ-related adverse effects, a partial agonist was designed to prevent the direct interaction with helix 12 of PPARγ-LBD. Because the TZD group is known to
RHO KINASE INHIBITORS
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Page/Page column 48-49, (2012/02/01)
The present invention relates to compounds of formula (I): and pharmaceutically acceptable salts thereof, wherein R1 and X are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of Rho Kinase-mediated disorders selected from hypertension, atherosclerosis, restenosis, stroke, myocardial infarction, heart failure, coronary artery disease, peripheral artery disease, coronary vasospasm, cerebral vasospasm, ischemia/reperfusion injury, pulmonary hypertension, angina, erectile dysfunction, renal disease, organ failure, asthma, glaucoma, cancer, Alzheimer's disease, multiple sclerosis, spinal cord injury, neuropathic pain, rheumatoid arthritis, psoriasis inflammatory bowel disease, and combinations of such disorders.
FUSED BICYCLIC HETEROARYL DERIVATIVES
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Page/Page column 65, (2010/01/07)
Problem to be Solved The present invention relates to a novel fused bicyclic heteroaryl derivative or a pharmacologically acceptable salt thereof, which has an excellent hypoglycemic effect or treats and/or prevents the onset of a disorder of carbohydrate