TY - JOUR
T1 - Synthesis of All Stereoisomers of RK460 and Evaluation of Their Activity and Selectivity as Abscisic Acid Receptor Antagonists
AU - Mikame, Yu
AU - Yoshida, Kazuko
AU - Hashizume, Daisuke
AU - Hirai, Go
AU - Nagasawa, Kazuo
AU - Osada, Hiroyuki
AU - Sodeoka, Mikiko
N1 - Funding Information:
This study was partially supported by the JSPS KAKENHI (Grant Numbers 16H01167, and 18H04417 for Middle Molecular Strat- egy and 16K18662, 17H06412, 18H02097, 18H03945), NARO Bio-oriented Technology Research Advancement Institution (Research program on development of innovative technology), AMED-CREST (JP18gm0710004), and RIKEN project funding. We also thank Dr. Shintaro Kawamura for his valuable technical advice.
Publisher Copyright:
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2019/3/7
Y1 - 2019/3/7
N2 - The PYR/PYL/RCAR protein families have recently emerged as receptors of the phytohormone abscisic acid (ABA, 1), which regulates plant responses to environmental stress. These families have multiple members with different physiological actions, and so selective agonists or antagonists are needed both as tools to elucidate functional differences and as lead compounds for agrochemicals. We previously identified RK460 (rac-3 a) as a PYR1-selective antagonist, and showed that it possesses five stereocenters on a 6,5-cis-bicyclo skeleton. Here, we synthesized all the stereoisomers of RK460 and evaluated their activity towards a panel of receptors. Relative stereochemistry as well as absolute stereochemistry was important for selective action.
AB - The PYR/PYL/RCAR protein families have recently emerged as receptors of the phytohormone abscisic acid (ABA, 1), which regulates plant responses to environmental stress. These families have multiple members with different physiological actions, and so selective agonists or antagonists are needed both as tools to elucidate functional differences and as lead compounds for agrochemicals. We previously identified RK460 (rac-3 a) as a PYR1-selective antagonist, and showed that it possesses five stereocenters on a 6,5-cis-bicyclo skeleton. Here, we synthesized all the stereoisomers of RK460 and evaluated their activity towards a panel of receptors. Relative stereochemistry as well as absolute stereochemistry was important for selective action.
UR - http://www.scopus.com/inward/record.url?scp=85061484666&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85061484666&partnerID=8YFLogxK
U2 - 10.1002/chem.201806056
DO - 10.1002/chem.201806056
M3 - Article
C2 - 30589135
AN - SCOPUS:85061484666
SN - 0947-6539
VL - 25
SP - 3496
EP - 3500
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 14
ER -