Bis(2,4-dioxy pyrimidinyl) di:one cpds

Uracil derivs. of formula (I) are new. (R=H or 1-4C alkyl). Pref. R1 is Me. (I) are pref. prepd. by reacting a cpd. with the formula X-COCO-X (X=halogen atom or 1-4C alkoxy gp.) with two or more times the mol quantity, pref. two times the mol quantity of a pyridine silylide of formula (II). (I) have...

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Hauptverfasser: MIKIO KUMAKURA, SEITARO KAJIYA, TATSURO YOKOYAMA, YUTAKA OKAZAKI, HIROSHI KAWAZURA, AKIRA AWYA, HIROSHI TOKUDA, ISAO SAKANO
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Sprache:eng ; ita
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Zusammenfassung:Uracil derivs. of formula (I) are new. (R=H or 1-4C alkyl). Pref. R1 is Me. (I) are pref. prepd. by reacting a cpd. with the formula X-COCO-X (X=halogen atom or 1-4C alkoxy gp.) with two or more times the mol quantity, pref. two times the mol quantity of a pyridine silylide of formula (II). (I) have immunity control effects and are suitable for treating chronic rheumatism, viral complaints and cancer, and have low toxicity. The estimated LD50 value in 7 day oral administration to ddY male mice was 1000 mg/kg or more. The dosage per 1 kg body wt. per day is suitably 1-30 mg for rectal application, 1-10 mg for intravenous injection and 1-30 mg for intramuscular or subcutaneous injection.