28713-99-7Relevant academic research and scientific papers
Asymmetrical ligand binding by abscisic acid 8′-hydroxylase
Ueno, Kotomi,Yoneyama, Hidetaka,Mizutani, Masaharu,Hirai, Nobuhiro,Todoroki, Yasushi
, p. 6311 - 6322 (2008/09/17)
Abscisic acid (ABA), a plant stress hormone, has a chiral center (C1′) in its molecule, yielding the enantiomers (1′S)-(+)-ABA and (1′R)-(-)-ABA during chemical synthesis. ABA 8′-hydroxylase (CYP707A), which is the major and key P450 enzyme in ABA catabol
THE METABOLISM OF α-IONYLIDENE COMPOUNDS BY CERCOSPORA ROSICOLA
Neill, Steven J.,Horgan, Roger,Walton, Daniel C.,Mercer, Carola A. M.
, p. 2515 - 2520 (2007/10/02)
α-Ionylidene ethanol was converted to 4'hydroxy-α-ionylidene acetic acid, 1'-deoxy-ABA and ABA by Cerospora rosicola.Both the 4'-(R)- and 4'-(S)-epimers of 4'-hydroxy-α-ionylidene acetic acid were detected but the configuration of the 1'-position was not
Ionylideneacetic Acids and Abscisic Acid Biosynthesis by Cercospora rosicola
Norman, Shirley M.,Poling, Stephen M.,Maier, V. P.,Nelson, Mary D.
, p. 2317 - 2324 (2007/10/02)
Several compounds having the basic α-ionylideneacetic acid stucture were tested in Cercospora rosicola resuspensions.At 100 μM, all the compounds inhibited abscisic acid (ABA) biosynthesis.Time studies with unlabelled and deuterated (2Z,4E)- and (2E,4E)-α
