-
1
-
-
0039302669
-
Dioxygen activation by enzymes with mononuclear non-heme iron active sites
-
Que, L.; Ho, R. Y. N. Dioxygen activation by enzymes with mononuclear non-heme iron active sites. Chem. Rev. 1996, 96, 2607-2624.
-
(1996)
Chem. Rev
, vol.96
, pp. 2607-2624
-
-
Que, L.1
Ho, R.Y.N.2
-
2
-
-
0030952515
-
A mechanistic rationalisation for the substrate specificity of recombinant mammalian 4-hydroxyphenylpyruvate dioxygenase
-
Crouch, N. P.; Adlington, R. M.; Baldwin, J. E.; Lee, M.-H.; MacKinnnon, C. H. A mechanistic rationalisation for the substrate specificity of recombinant mammalian 4-hydroxyphenylpyruvate dioxygenase. Tetrahedron 1997, 53, 6993-7010.
-
(1997)
Tetrahedron
, vol.53
, pp. 6993-7010
-
-
Crouch, N.P.1
Adlington, R.M.2
Baldwin, J.E.3
Lee, M.-H.4
MacKinnnon, C.H.5
-
3
-
-
0021824504
-
Alternate substrates and inhibitors of bacterial 4-hydroxyphenylpyruvate dioxygenase
-
Pascal, R. A.; Oliver, M. A.; Chen, Y. C. J. Alternate substrates and inhibitors of bacterial 4-hydroxyphenylpyruvate dioxygenase. Biochemistry 1985, 24, 3158-3165.
-
(1985)
Biochemistry
, vol.24
, pp. 3158-3165
-
-
Pascal, R.A.1
Oliver, M.A.2
Chen, Y.C.J.3
-
4
-
-
0029556712
-
Genetic dissection of carotenoid synthesis in Arabidopsis defines plastoquinone as an essential component of phytoene desaturation
-
Norris, S. R.; Barrette, T. R.; DellaPenna, D. Genetic dissection of carotenoid synthesis in Arabidopsis defines plastoquinone as an essential component of phytoene desaturation. Plant Cell 1995, 7, 2139-2149.
-
(1995)
Plant Cell
, vol.7
, pp. 2139-2149
-
-
Norris, S.R.1
Barrette, T.R.2
DellaPenna, D.3
-
5
-
-
0031760410
-
The mode of action of isoxaflutole I. Physiological effects, metabolism, and selectivity
-
Pallett, K. E.; Little, J. P.; Sheekey, M.; Veerasekaran, P. The mode of action of isoxaflutole I. Physiological effects, metabolism, and selectivity. Pestic. Biochem. Physiol. 1998, 62, 113-124.
-
(1998)
Pestic. Biochem. Physiol
, vol.62
, pp. 113-124
-
-
Pallett, K.E.1
Little, J.P.2
Sheekey, M.3
Veerasekaran, P.4
-
6
-
-
0027452908
-
SC-0051, a 2-benzoylcyclohexane-l,3-dione bleaching herbicide, is a potent inhibitor of the enzyme p-hydroxyphenylpyruvate dioxygenase
-
Schulz, A.; Ort, O.; Beyer, P.; Kleinig, H. SC-0051, a 2-benzoylcyclohexane-l,3-dione bleaching herbicide, is a potent inhibitor of the enzyme p-hydroxyphenylpyruvate dioxygenase. FEBS Lett. 1993, 318,162-166.
-
(1993)
FEBS Lett
, vol.318
, pp. 162-166
-
-
Schulz, A.1
Ort, O.2
Beyer, P.3
Kleinig, H.4
-
7
-
-
0030752735
-
The discovery and structural requirements of inhibitors of p-hydroxyphenylpyruvate dioxygenase
-
Lee, D. L.; Prisbylla, M. P.; Cromartie, T. H.; Dagarin, D. P.; Howard, S. W.; Provan, W. M.; Ellis, M. K.; Fraser, T.; Mutter, L. C. The discovery and structural requirements of inhibitors of p-hydroxyphenylpyruvate dioxygenase. Weed Sei. 1997, 45, 601-609.
-
(1997)
Weed Sei
, vol.45
, pp. 601-609
-
-
Lee, D.L.1
Prisbylla, M.P.2
Cromartie, T.H.3
Dagarin, D.P.4
Howard, S.W.5
Provan, W.M.6
Ellis, M.K.7
Fraser, T.8
Mutter, L.C.9
-
8
-
-
0031789261
-
The mode of action of isoxaflutole II. Characterization of the inhibition of carrot 4-hydroxyphenylpyruvate dioxygenase by the diketonitrile derivative of isoxaflutole
-
Viviani, E.; Little, J. P.; Pallett, K. E. The mode of action of isoxaflutole II. Characterization of the inhibition of carrot 4-hydroxyphenylpyruvate dioxygenase by the diketonitrile derivative of isoxaflutole. Pestic. Biochem. Physiol. 1998, 62, 125-134.
-
(1998)
Pestic. Biochem. Physiol
, vol.62
, pp. 125-134
-
-
Viviani, E.1
Little, J.P.2
Pallett, K.E.3
-
9
-
-
0031754019
-
Structure-toxicity relationships for selected naphthoquinones to Tetrahymena pyriformis
-
Schultz, T. W.; Bearden, A. P. Structure-toxicity relationships for selected naphthoquinones to Tetrahymena pyriformis. Bull. Environ. Contam. Toxicol. 1998, 61, 405-410.
-
(1998)
Bull. Environ. Contam. Toxicol
, vol.61
, pp. 405-410
-
-
Schultz, T.W.1
Bearden, A.P.2
-
10
-
-
0003634569
-
-
9th ed, Weed Science Society of America: Lawrence, KS
-
Senseman, S. A. Herbicide Handbook, 9th ed.; Weed Science Society of America: Lawrence, KS, 2007; p 458.
-
(2007)
Herbicide Handbook
, pp. 458
-
-
Senseman, S.A.1
-
11
-
-
44349160015
-
Genetic basis of sensitivity in sweet corn to tembotrione
-
Williams, M. M.; Pataky, J. K. Genetic basis of sensitivity in sweet corn to tembotrione. Weed Sci. 2008, 56, 364-370.
-
(2008)
Weed Sci
, vol.56
, pp. 364-370
-
-
Williams, M.M.1
Pataky, J.K.2
-
12
-
-
0031774552
-
The structure-activity relationships of the triketone class of HPPD herbicides
-
Lee, D. L.; Knudsen, C. G.; Michaely, W. J.; Chin, H.-L.; Nguyen, N. H.; Carter, C. G.; Cromartie, T. H.; Lake, B. H.; Shribbs, J. M.; Fraser, T. The structure-activity relationships of the triketone class of HPPD herbicides. Pestic. Sci. 1998, 54, 377-384.
-
(1998)
Pestic. Sci
, vol.54
, pp. 377-384
-
-
Lee, D.L.1
Knudsen, C.G.2
Michaely, W.J.3
Chin, H.-L.4
Nguyen, N.H.5
Carter, C.G.6
Cromartie, T.H.7
Lake, B.H.8
Shribbs, J.M.9
Fraser, T.10
-
13
-
-
67649238980
-
-
Gray, R. A.; Tseng, C. K.; Rusay, R. J. l-Hydroxy-2-(alkylketo)4,4,6,6- tetramethyl cyclohexen-3,5-dione herbicides. U.S. Patent 4,227,919, 1980.
-
Gray, R. A.; Tseng, C. K.; Rusay, R. J. l-Hydroxy-2-(alkylketo)4,4,6,6- tetramethyl cyclohexen-3,5-dione herbicides. U.S. Patent 4,227,919, 1980.
-
-
-
-
14
-
-
2942586865
-
Essential oils from New Zealand manuka: Triketone and other chemotypes of Leptospermum scoparium
-
Douglas, M. H.; van Klink, J. W.; Smallfield, B. M.; Perry, N. B.; Anderson, R. E.; Johnstone, P.; Weavers, R. T. Essential oils from New Zealand manuka: triketone and other chemotypes of Leptospermum scoparium. Phytochemistry 2004, 65, 1255-1264.
-
(2004)
Phytochemistry
, vol.65
, pp. 1255-1264
-
-
Douglas, M.H.1
van Klink, J.W.2
Smallfield, B.M.3
Perry, N.B.4
Anderson, R.E.5
Johnstone, P.6
Weavers, R.T.7
-
15
-
-
84970548689
-
The occurrence of β-triketones in the steam-volatile oils of some myrtaceous australian plants
-
Hellyer, R. O. The occurrence of β-triketones in the steam-volatile oils of some myrtaceous australian plants. Aust. J. Chem 1968, 21, 2825-2828.
-
(1968)
Aust. J. Chem
, vol.21
, pp. 2825-2828
-
-
Hellyer, R.O.1
-
16
-
-
0032944337
-
Triketones from myrtaceae: Isoleptospermone from Leptospermum scoparium and papuanone from Corymbia dallachiana
-
van Klink, J. W.; Brophy, N. B.; Perry, N. B.; Weavers, R. T. Triketones from myrtaceae: isoleptospermone from Leptospermum scoparium and papuanone from Corymbia dallachiana. J. Nat. Prod. 1999, 62, 487-489.
-
(1999)
J. Nat. Prod
, vol.62
, pp. 487-489
-
-
van Klink, J.W.1
Brophy, N.B.2
Perry, N.B.3
Weavers, R.T.4
-
17
-
-
0033837211
-
Leaf essential oils of the genus Leptospermum (Myrtaceae) in eastern Australia. Part 6. Leptospermum polygalifolium and allies
-
Brophy, J. J.; Goldsack, R. J.; Bean, A. R.; Forster, P. I.; Lepschi, B. J. Leaf essential oils of the genus Leptospermum (Myrtaceae) in eastern Australia. Part 6. Leptospermum polygalifolium and allies. Flavour Fragrance J. 2000,15, 271-277.
-
(2000)
Flavour Fragrance J
, vol.15
, pp. 271-277
-
-
Brophy, J.J.1
Goldsack, R.J.2
Bean, A.R.3
Forster, P.I.4
Lepschi, B.J.5
-
18
-
-
21444433418
-
2-Acylcycloalkane1,3- diones
-
Rubinov, D. B.; Rubinova, I. L.; Akhrem, A. A. 2-Acylcycloalkane1,3- diones. Chem. Nat. Compd. 1995, 31, 537-559.
-
(1995)
Chem. Nat. Compd
, vol.31
, pp. 537-559
-
-
Rubinov, D.B.1
Rubinova, I.L.2
Akhrem, A.A.3
-
19
-
-
27644497906
-
Triketones active against antibiotic-resistant bacteria: Synthesis, structure-activity relationships, and mode of action
-
van Klink, J. W.; Larsen, L.; Perry, N. B.; Weavers, R. T.; Cook, G. M.; Bremer, P. J.; MacKenzie, A. D.; Kirika, T. Triketones active against antibiotic-resistant bacteria: synthesis, structure-activity relationships, and mode of action. Bioorg. Med. Chem. 2005, 13, 6651-6662.
-
(2005)
Bioorg. Med. Chem
, vol.13
, pp. 6651-6662
-
-
van Klink, J.W.1
Larsen, L.2
Perry, N.B.3
Weavers, R.T.4
Cook, G.M.5
Bremer, P.J.6
MacKenzie, A.D.7
Kirika, T.8
-
20
-
-
0033881387
-
A comparative study of the in vitro antimicrobial activity of tea tree oils with special reference to the activity of β-triketones
-
Christoph, F.; Kaulfers, P.-M.; Stahl-Biskup, E. A comparative study of the in vitro antimicrobial activity of tea tree oils with special reference to the activity of β-triketones. Planta Med. 2000, 66, 556-560.
-
(2000)
Planta Med
, vol.66
, pp. 556-560
-
-
Christoph, F.1
Kaulfers, P.-M.2
Stahl-Biskup, E.3
-
21
-
-
84869299677
-
-
Spooner-Hart, R. N.; Basta, A. H. Pesticidal compositions containing β-diketones and β-triketones from essential oils. Pct. Int. Appl. Coden PIXXD2 WO 2002089587, AI 20021114, CAN 137:347894, AN 2002:868663, 2002; 88 pp.
-
Spooner-Hart, R. N.; Basta, A. H. Pesticidal compositions containing β-diketones and β-triketones from essential oils. Pct. Int. Appl. Coden PIXXD2 WO 2002089587, AI 20021114, CAN 137:347894, AN 2002:868663, 2002; 88 pp.
-
-
-
-
22
-
-
0000748357
-
The composition of commercial manuka oils from New Zealand
-
Christoph, F.; Kubeczka, K. H.; Stahl-Biskup, E. The composition of commercial manuka oils from New Zealand. J. Essent. Oil Res. 1999, 11, 705-710.
-
(1999)
J. Essent. Oil Res
, vol.11
, pp. 705-710
-
-
Christoph, F.1
Kubeczka, K.H.2
Stahl-Biskup, E.3
-
23
-
-
30844444386
-
Virucidal activity of a β-triketone-rich essential oil oí Leptospermum scoparium (manuka oil) against HSV-1 and HSV-2 in cell culture
-
Reichling, J.; Koch, C; Stahl-Biskup, E.; Sojka, C; Schnitzler, P. Virucidal activity of a β-triketone-rich essential oil oí Leptospermum scoparium (manuka oil) against HSV-1 and HSV-2 in cell culture. Planta Med. 2005, 71, 1123-1127.
-
(2005)
Planta Med
, vol.71
, pp. 1123-1127
-
-
Reichling, J.1
Koch, C.2
Stahl-Biskup, E.3
Sojka, C.4
Schnitzler, P.5
-
24
-
-
0010078138
-
Discovery of the triketone class of HPPD inhibiting herbicides and their relationship to naturally occurring β-triketones
-
Narwal, S. S, Ed, Kluwer Academic Publishers: Dordrecht, The Netherlands
-
Knudsen, C. G.; Lee, D. L.; Michaely, W. J.; Chin, H.-L.; Nguyen, N. H.; Rusay, R. J.; Cromartie, T. H.; Gray, R.; Lake, B. H.; Fraser, T. E. M.; Cartwright, D. Discovery of the triketone class of HPPD inhibiting herbicides and their relationship to naturally occurring β-triketones. In Allelopathy in Ecological Agriculture and Forestry; Narwal, S. S., Ed.; Kluwer Academic Publishers: Dordrecht, The Netherlands, 2000; pp 101-111.
-
(2000)
Allelopathy in Ecological Agriculture and Forestry
, pp. 101-111
-
-
Knudsen, C.G.1
Lee, D.L.2
Michaely, W.J.3
Chin, H.-L.4
Nguyen, N.H.5
Rusay, R.J.6
Cromartie, T.H.7
Gray, R.8
Lake, B.H.9
Fraser, T.E.M.10
Cartwright, D.11
-
25
-
-
34447103297
-
-
Dayan, F. E.; Duke, S. O.; Sauldubois, A.; Singh, N.; McCurdy, C; Cantrell, C. L. p-Hydroxyphenylpyruvate dioxygenase is a herbicidal target site for β-triketones from Leptospermum scoparium. Phytochemistry 2007, 68, 2004-2014.
-
Dayan, F. E.; Duke, S. O.; Sauldubois, A.; Singh, N.; McCurdy, C; Cantrell, C. L. p-Hydroxyphenylpyruvate dioxygenase is a herbicidal target site for β-triketones from Leptospermum scoparium. Phytochemistry 2007, 68, 2004-2014.
-
-
-
-
26
-
-
0033117526
-
Characterization and subcellular compartmentation of recombinant 4-hydroxyphenylpyruvate dioxygenase from Arabidopsis in transgenic tobacco
-
Garcia, I.; Rodgers, M.; Pepin, R.; Hsieh, T.-Z.; Matringe, M. Characterization and subcellular compartmentation of recombinant 4-hydroxyphenylpyruvate dioxygenase from Arabidopsis in transgenic tobacco. Plant Physiol. 1999,119, 1507-1516.
-
(1999)
Plant Physiol
, vol.119
, pp. 1507-1516
-
-
Garcia, I.1
Rodgers, M.2
Pepin, R.3
Hsieh, T.-Z.4
Matringe, M.5
-
28
-
-
28444445926
-
-
R-Development-Core-Team, 2.2.1; R Foundation for Statistical Computing: Vienna, Austria
-
R-Development-Core-Team. R: A Language and Environment for Statistical Computing, 2.2.1; R Foundation for Statistical Computing: Vienna, Austria, 2005.
-
(2005)
R: A Language and Environment for Statistical Computing
-
-
-
29
-
-
4043073398
-
Structural basis for herbicidal inhibitor selectivity revealed by comparison of crystal structures of plant and mammalian 4-hydroxyphenylpyruvate dioxygenases
-
Yang, C; Pflugrath, J. W.; Camper, D. L.; Foster, M. L.; Pernich, D. J.; Walsh, T. A. Structural basis for herbicidal inhibitor selectivity revealed by comparison of crystal structures of plant and mammalian 4-hydroxyphenylpyruvate dioxygenases. Biochemistry 2004,43, 10414-10423.
-
(2004)
Biochemistry
, vol.43
, pp. 10414-10423
-
-
Yang, C.1
Pflugrath, J.W.2
Camper, D.L.3
Foster, M.L.4
Pernich, D.J.5
Walsh, T.A.6
-
30
-
-
2542568185
-
Structure of the ferrous form of (4-hydroxyphenyl)pyruvate dioxygenase from Streptomyces avermitilis in complex with the therapeutic herbicide, NTBC
-
Brownlee, J. M.; Johnson-Winters, K.; Harrison, D. H.; Moran, G. R. Structure of the ferrous form of (4-hydroxyphenyl)pyruvate dioxygenase from Streptomyces avermitilis in complex with the therapeutic herbicide, NTBC. Biochemistry 2004, 43, 6370-6377.
-
(2004)
Biochemistry
, vol.43
, pp. 6370-6377
-
-
Brownlee, J.M.1
Johnson-Winters, K.2
Harrison, D.H.3
Moran, G.R.4
-
31
-
-
0023751431
-
Comparative molecular field analysis (CoMFA). Effect of shape of binding of steroids to carrier proteins
-
Cramer, R. D. I.; Patterson, D. E.; Bunce, J. D. Comparative molecular field analysis (CoMFA). Effect of shape of binding of steroids to carrier proteins. J. Am. Chem. Soc. 1988,110,5959-5967.
-
(1988)
J. Am. Chem. Soc
, vol.110
, pp. 5959-5967
-
-
Cramer, R.D.I.1
Patterson, D.E.2
Bunce, J.D.3
-
32
-
-
11944251068
-
Maximally diagonal force constants in dependent angle-bending coordinates. II. Implications for the design of empirical force fields
-
Halgren, T. A. Maximally diagonal force constants in dependent angle-bending coordinates. II. Implications for the design of empirical force fields. J. Am. Chem. Soc. 1990,112, 4723-4728.
-
(1990)
J. Am. Chem. Soc
, vol.112
, pp. 4723-4728
-
-
Halgren, T.A.1
-
33
-
-
0026292147
-
HINT: A new method of empirical hydrophobic field calculation for CoMFA
-
Kellogg, G. E.; Semus, S. F.; Abraham, D. J. HINT: a new method of empirical hydrophobic field calculation for CoMFA. J. Comput.Aid. Mol. Des. 1991, 5, 545-552.
-
(1991)
J. Comput.Aid. Mol. Des
, vol.5
, pp. 545-552
-
-
Kellogg, G.E.1
Semus, S.F.2
Abraham, D.J.3
-
34
-
-
4544345612
-
Oxidative fragmentation of the bridged β-triketone core of hyperforin
-
Verotta, L.; Lovaglio, E.; Sterner, O.; Appendino, G.; Bombardelli, E. Oxidative fragmentation of the bridged β-triketone core of hyperforin. Eur. J. Org. Chem. 2004, 6, 1193-1197.
-
(2004)
Eur. J. Org. Chem
, vol.6
, pp. 1193-1197
-
-
Verotta, L.1
Lovaglio, E.2
Sterner, O.3
Appendino, G.4
Bombardelli, E.5
-
35
-
-
0019422535
-
Dihydrochalcone sweeteners - a study of the atypical temporal phenomena
-
DuBois, G. E.; Crosby, G. A.; Stephenson, R. A. Dihydrochalcone sweeteners - a study of the atypical temporal phenomena. J. Med. Chem. 1981, 24, 408-428.
-
(1981)
J. Med. Chem
, vol.24
, pp. 408-428
-
-
DuBois, G.E.1
Crosby, G.A.2
Stephenson, R.A.3
-
36
-
-
0029189074
-
Functional anatomy of the oil glands of Melaleuca alternifolia (Myrtaceae)
-
List, S.; Brown, P. H.; Walsh, K. B. Functional anatomy of the oil glands of Melaleuca alternifolia (Myrtaceae). Aust. J. Bot. 1995, 43, 629-641.
-
(1995)
Aust. J. Bot
, vol.43
, pp. 629-641
-
-
List, S.1
Brown, P.H.2
Walsh, K.B.3
-
37
-
-
0041784773
-
Trichomes and root hairs: Natural pesticide factories
-
Dayan, F. E.; Duke, S. O. Trichomes and root hairs: natural pesticide factories. Pestic. Outlook 2003, 4, 175-178.
-
(2003)
Pestic. Outlook
, vol.4
, pp. 175-178
-
-
Dayan, F.E.1
Duke, S.O.2
-
38
-
-
45849101363
-
Mechanisms of resistance to self-produced toxic secondary metabolites in plants
-
Sirikantaramas, S.; Yamakazi, M.; Saito, K. Mechanisms of resistance to self-produced toxic secondary metabolites in plants. Phytochem. Rev. 2008, 7, 467-477.
-
(2008)
Phytochem. Rev
, vol.7
, pp. 467-477
-
-
Sirikantaramas, S.1
Yamakazi, M.2
Saito, K.3
-
39
-
-
0037030803
-
The inhibitory activity of natural products on plant p- hydroxyphenylpyruvate dioxygenase
-
Meazza, G.; Scheffler, B. E.; Tellez, M. R.; Rimando, A. M.; Nanayakkara, N. P. D.; Khan, I. A.; Abourashed, E. A.; Romagni, J. G.; Duke, S. O.; Dayan, F. E. The inhibitory activity of natural products on plant p- hydroxyphenylpyruvate dioxygenase. Phytochemistry 2002, 59, 281-288.
-
(2002)
Phytochemistry
, vol.59
, pp. 281-288
-
-
Meazza, G.1
Scheffler, B.E.2
Tellez, M.R.3
Rimando, A.M.4
Nanayakkara, N.P.D.5
Khan, I.A.6
Abourashed, E.A.7
Romagni, J.G.8
Duke, S.O.9
Dayan, F.E.10
-
40
-
-
0343517556
-
Hydrophobicity: Is LogPo/w more than the sum of its parts?
-
Kellogg, G. E.; Abraham, D. J. Hydrophobicity: is LogPo/w more than the sum of its parts?. Eur. J. Med. Chem. 2000, 35, 651-661.
-
(2000)
Eur. J. Med. Chem
, vol.35
, pp. 651-661
-
-
Kellogg, G.E.1
Abraham, D.J.2
-
41
-
-
0842344659
-
Three-dimensional modeling of plant 4-hydroxyphenylpyruvate dioxygenase, a molecular target of triketone-type herbicides
-
Kakidani, H.; Hirai, K. Three-dimensional modeling of plant 4-hydroxyphenylpyruvate dioxygenase, a molecular target of triketone-type herbicides. J. Pestic. Sci. 2003, 28, 409-415.
-
(2003)
J. Pestic. Sci
, vol.28
, pp. 409-415
-
-
Kakidani, H.1
Hirai, K.2
-
42
-
-
0030054012
-
-
Ellis, M. K.; Whitfield, A. C; Gowans, L. A.; Auton, T. R.; Provan, W. M.; Lock, E. A.; Lee, D. L.; Smith, L. L. Characterization of the interaction of 2-[2-nitro-4-(trifluoromethyl)benzoyl]-4,4,6,6-tetramethylcyclohexane-l,3,5- trione with rat hepatic 4-hydroxyphenylpyruvate dioxygenase. Chem. Res. Toxicol. 1996, 9, 24-27.
-
Ellis, M. K.; Whitfield, A. C; Gowans, L. A.; Auton, T. R.; Provan, W. M.; Lock, E. A.; Lee, D. L.; Smith, L. L. Characterization of the interaction of 2-[2-nitro-4-(trifluoromethyl)benzoyl]-4,4,6,6-tetramethylcyclohexane-l,3,5- trione with rat hepatic 4-hydroxyphenylpyruvate dioxygenase. Chem. Res. Toxicol. 1996, 9, 24-27.
-
-
-
-
43
-
-
0037009202
-
3D-QSAR studies on 4-hydroxyphenylpyruvate dioxygenase inhibitors by comparative molecular field analysis (CoMFA)
-
Huang, M.; Yang, D.-Y.; Shang, Z.; Zou, J.; Yu, Q. 3D-QSAR studies on 4-hydroxyphenylpyruvate dioxygenase inhibitors by comparative molecular field analysis (CoMFA). Bioorg. Med. Chem. Lett. 2002,12, 2271-2275.
-
(2002)
Bioorg. Med. Chem. Lett
, vol.12
, pp. 2271-2275
-
-
Huang, M.1
Yang, D.-Y.2
Shang, Z.3
Zou, J.4
Yu, Q.5
|