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Coronalon: a powerful tool in plant stress physiology

MPS-Authors
http://pubman.mpdl.mpg.de/cone/persons/resource/persons4167

Schüler,  G.
Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons4052

Mithöfer,  A.
Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons3786

Baldwin,  I. T.
Department of Molecular Ecology, MPI for Chemical Ecology, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons3936

Hölscher,  D.
Research Group Biosynthesis / NMR, MPI for Chemical Ecology, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons4159

Schneider,  B.
Research Group Biosynthesis / NMR, MPI for Chemical Ecology, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons3812

Boland,  W.
Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society;

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Citation

Schüler, G., Mithöfer, A., Baldwin, I. T., Berger, S., Ebel, S., Santos, J. G., et al. (2004). Coronalon: a powerful tool in plant stress physiology. FEBS Letters, 563(1-3), 17-22. doi:10.1016/S0014-5793(04)00239-X.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0012-A349-9
Abstract
Coronalon, a synthetic 6-ethyl indanoyl isoleucine conjugate, has been designed as a highly active mimic of octadecanoid phytohormones that are involved in insect and disease resistance. The spectrum of biological activities that is affected by coronalo