The inhibitory activity of natural products on plant p-hydroxyphenylpyruvate dioxygenase.
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S. Duke | F. Dayan | A. Rimando | B. Scheffler | I. Khan | E. Abourashed | M. R. Tellez | J. Romagni | G. Meazza | D. Nanayakkara | M. Tellez
[1] S. S. Narwal,et al. Allelopathy in Ecological Agriculture and Forestry , 2012, Springer Netherlands.
[2] D. C. Holt,et al. Mesotrione: a new selective herbicide for use in maize. , 2001, Pest management science.
[3] F. Dayan,et al. The phytotoxic lichen metabolite, usnic acid, is a potent inhibitor of plant p‐hydroxyphenylpyruvate dioxygenase , 2000, FEBS letters.
[4] D. Job,et al. Inhibition of p-hydroxyphenylpyruvate dioxygenase by the diketonitrile of isoxaflutole: a case of half-site reactivity. , 2000, Biochemistry.
[5] C. G. Carter,et al. The structure–activity relationships of the triketone class of HPPD herbicides† , 1998 .
[6] K. Pallett,et al. The Mode of Action of Isoxaflutole II. Characterization of the Inhibition of Carrot 4-Hydroxyphenylpyruvate Dioxygenase by the Diketonitrile Derivative of Isoxaflutole☆☆☆ , 1998 .
[7] K. Pallett,et al. The Mode of Action of Isoxaflutole: I. Physiological Effects, Metabolism, and Selectivity , 1998 .
[8] Dayan,et al. A new photosystem II electron transfer inhibitor from sorghum bicolor , 1998, Journal of natural products.
[9] T. Fraser,et al. The discovery and structural requirements of inhibitors of p-hydroxyphenylpyruvate dioxygenase , 1997, Weed Science.
[10] J. Baldwin,et al. A mechanistic rationalisation for the substrate specificity of recombinant mammalian 4-hydroxyphenylpyruvate dioxygenase (4-HPPD) , 1997 .
[11] R. Ho,et al. Dioxygen Activation by Enzymes with Mononuclear Non-Heme Iron Active Sites. , 1996, Chemical reviews.
[12] E. Lock,et al. Inhibition of 4-hydroxyphenylpyruvate dioxygenase by 2-(2-nitro-4-trifluoromethylbenzoyl)-cyclohexane-1,3-dione and 2-(2-chloro-4-methanesulfonylbenzoyl)-cyclohexane-1,3-dione. , 1995, Toxicology and applied pharmacology.
[13] A. Schulz,et al. SC‐0051, a 2‐benzoyl‐cyclohexane‐1,3‐dione bleaching herbicide, is a potent inhibitor of the enzyme p‐hydroxyphenylpyruvate dioxygenase , 1993, FEBS letters.
[14] R. Pascal,et al. Alternate substrates and inhibitors of bacterial 4-hydroxyphenylpyruvate dioxygenase. , 1985, Biochemistry.
[15] S. Lindstedt,et al. The mechanism of enzymic formation of homogentisate from p-hydroxyphenylpyruvate. , 1970, Journal of the American Chemical Society.
[16] Christopher G. Knudsen,et al. Discovery of the triketone class of HPPD inhibiting herbicides and their relationship to naturally occurring β-triketones , 2000 .
[17] E. Lock,et al. Characterization of the interaction of 2-[2-nitro-4-(trifluoromethyl)benzoyl]-4,4,6,6,-tetramethyl- cyclohexane-1,3,5-trione with rat hepatic 4-hydroxyphenylpyruvate dioxygenase. , 1996, Chemical research in toxicology.
[18] J. Beraud,et al. ICIA0051, a new herbicide for the control of annual weeds in maize , 1991 .
[19] R. Hellyer. The occurrence of β-triketones in the steam-volatile oils of some myrtaceous Australian plants , 1968 .