TY  - GEN
AU  - Rikimaru,Kentaro
AU  - Wakabayashi,Takeshi
AU  - Abe,Hidenori
AU  - Tawaraishi,Taisuke
AU  - Imoto,Hiroshi
AU  - Yonemori,Jinichi
AU  - Hirose,Hideki
AU  - Murase,Katsuhito
AU  - Matsuo,Takanori
AU  - Matsumoto,Mitsuharu
AU  - Nomura,Chisako
AU  - Tsuge,Hiroko
AU  - Arimura,Naoto
AU  - Kawakami,Kazutoshi
AU  - Sakamoto,Junichi
AU  - Funami,Miyuki
AU  - Mol,Clifford D
AU  - Snell,Gyorgy P
AU  - Bragstad,Kenneth A
AU  - Sang,Bi-Ching
AU  - Dougan,Douglas R
AU  - Tanaka,Toshimasa
AU  - Katayama,Nozomi
AU  - Horiguchi,Yoshiaki
AU  - Momose,Yu
TI  - Structure-activity relationships and key structural feature of pyridyloxybenzene-acylsulfonamides as new, potent, and selective peroxisome proliferator-activated receptor (PPAR) γ Agonists
SN  - 1464-3391
PY  - 2012///0810
KW  - Acylation
KW  - Animals
KW  - Binding Sites
KW  - Blood Glucose
KW  - drug effects
KW  - CHO Cells
KW  - COS Cells
KW  - Chlorocebus aethiops
KW  - Cricetinae
KW  - Crystallography, X-Ray
KW  - Drug Design
KW  - Humans
KW  - Hypoglycemic Agents
KW  - chemistry
KW  - Male
KW  - Models, Molecular
KW  - Peroxisome Proliferator-Activated Receptors
KW  - agonists
KW  - Protein Binding
KW  - Pyridines
KW  - administration & dosage
KW  - Rats, Wistar
KW  - Structure-Activity Relationship
KW  - Sulfonamides
N1  - Publication Type: Journal Article; Research Support, U.S. Gov't, Non-P.H.S
UR  - https://doi.org/10.1016/j.bmc.2012.03.036
ER  -