Abstract |
In reactions of 5-aminoisothiazolopyrimidines 1 with glycosilisothiocyanates and phenyl isocyano- or isocyanates, N-glycosilo-N-phenylo- and N-isothiazolopyrimidinothiocarbamides type II were obtained. The same compound--5-aminoisothiazolopyrimidine 1 in reaction with glucose, arabinose and ribose bromoderivatives was converted into N-glycosiloaminoisothiazolopyrimidies type 3. Some of the newly synthetized compounds appeared effective against L-1210 leukemia and Sa-180 sarcoma.
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Authors | Z Machoń, I Mielczarek, J Wieczorek, M Mordarski |
Journal | Archivum immunologiae et therapiae experimentalis
(Arch Immunol Ther Exp (Warsz))
Vol. 35
Issue 5
Pg. 609-16
( 1987)
ISSN: 0004-069X [Print] Switzerland |
PMID | 3455650
(Publication Type: Journal Article)
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Chemical References |
- Antineoplastic Agents
- Pyrimidines
- Thiazoles
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Topics |
- Animals
- Antineoplastic Agents
(chemical synthesis, therapeutic use)
- Cell Division
(drug effects)
- Chemical Phenomena
- Chemistry
- Drug Screening Assays, Antitumor
- Leukemia L1210
(drug therapy, mortality, pathology)
- Mice
- Pyrimidines
(chemical synthesis, therapeutic use)
- Sarcoma, Experimental
(drug therapy, mortality, pathology)
- Thiazoles
(chemical synthesis, therapeutic use)
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