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Relationships between Structure and Cytotoxicity of Thiourea Derivatives

Franke, R., Vasilev, G. N. and Dove, Stefan (1979) Relationships between Structure and Cytotoxicity of Thiourea Derivatives. Doklady Bolgarskoj Akademii Nauk (Sofia) 32 (3), pp. 369-375.

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The relations between the chem structure of the title compds. (I; R1 = Cl, OH, Me, NHAc, OMe; R2 = H, Cl, Me, OMe, NO2; R3 = alkyl or Ph; n = 1 or 2) and their cytotoxicity were studied by the technique of discriminant anal. To est. the effects of substituents in the substituted Ph ring on cytotoxicity, the hydrophobic substituent const., the Hammett const., and Taft's steric const. were used. ...


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Item type:Article
Institutions:Chemistry and Pharmacy > Institute of Pharmacy > Pharmaceutical/Medicinal Chemistry II (Prof. Buschauer)
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Dewey Decimal Classification:500 Science > 570 Life sciences
500 Science > 540 Chemistry & allied sciences
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:No
Item ID:5437
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