Structure-activity relationships in the developmental toxicity of substituted phenols: In vivo effects

Teratology ◽  
1990 ◽  
Vol 41 (1) ◽  
pp. 43-59 ◽  
Author(s):  
Robert J. Kavlock
ChemInform ◽  
2011 ◽  
Vol 42 (35) ◽  
pp. no-no
Author(s):  
Jun-ichi Kuroyanagi ◽  
Kazuo Kanai ◽  
Takao Horiuchi ◽  
Hiroshi Takeshita ◽  
Shozo Kobayashi ◽  
...  

1991 ◽  
Vol 16 (2) ◽  
pp. 225-229
Author(s):  
R. J. KAVLOCK ◽  
L. A. OGLESBY ◽  
L. L. HALL ◽  
H. L. FISHER ◽  
F. COPELAND ◽  
...  

2009 ◽  
Vol 76 (1) ◽  
pp. 58-67 ◽  
Author(s):  
Ester Gutiérrez-Pascual ◽  
Jérôme Leprince ◽  
Antonio J. Martínez-Fuentes ◽  
Isabelle Ségalas-Milazzo ◽  
Rafael Pineda ◽  
...  

1989 ◽  
Vol 44 (1-2) ◽  
pp. 85-96 ◽  
Author(s):  
E. Ebert ◽  
W. Eckhardt ◽  
K. Jäkel ◽  
D. Sozzi ◽  
C. Vogel ◽  
...  

Abstract The preparation of the four stereoisomers of propiconazole (TILT®) is described. Their inhibition of the 14α-C-demethylation of the sterol nucleus is examined and compared with the inhibition by the four stereoisomers of etaconazole (SONAX®). The quantitative structure-activity relationships (QSAR) of substituted 1,3-dioxolane-2-yl-methyltriazoles and 1,3-dioxane-2-ylmethyltriazoles on in vivo fungicidal activity are investigated.


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