Cytotoxic sulphonamides designed for selective deposition in malignant tissue
- 30 November 1975
- journal article
- Published by Elsevier in European Journal of Cancer (1965)
- Vol. 11 (11), 787-793
- https://doi.org/10.1016/0014-2964(75)90172-3
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
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- Synthese de la sulfadiazine et de ses derives : LA (N4 ‐ acetylsulfani lamido) ‐ ‐2 pyrimidine, la (bennzenesulfonamito) ‐2 pyrimidine et la (P ‐ toluenesulfonamido) ‐ 2 pyrimidine marquees par le 14C dans le noyau pyrimidineJournal of Labelled Compounds and Radiopharmaceuticals, 1973
- Synthesen radioaktiv markierter Verbindungen; Synthese von N‐Phenyl‐N'‐dimethylharnstoff(Fenuron)‐[Phenyl‐14C] und N‐Phenyl‐N'‐dimethylharnstoff(Fenuron)‐[14CH3] bzw. N‐(p‐Chlorphenyl)‐N'‐dimethylharnstoff(Monuron‐[14CH3]Zeitschrift für Chemie, 1969
- Aryl-2-halogenoalkylamines: XXV. Derivatives of sulphanilamide designed for selective deposition in neoplastic tissueEuropean Journal of Cancer (1965), 1968
- Sulfapyrazine Precipitated in Cancer Tissue upon Repeated Glucose InjectionsScience, 1950