摘要:
AND SALTS THEREOF WITH PHARMACOLOGICALLY ACCEPTABLE ACIDS. The invention furthermore is related to processes for the production thereof. The new compounds of formula I are useful as antiviral agents.
The present invention is related to certain new basically substituted cyclic urea derivatives having the general formula I
摘要翻译:本发明涉及一些新的基本上取代的具有通式I的化合物的环脲衍生物,其与具有药理学上可接受的酸的盐相比,其平均值为N-CO-A-R-N角度N-R1 I R3(CH2)m。 本发明还涉及其生产方法。 新的式I化合物可用作抗病毒剂。
摘要:
THERE ARE PROVIDED NEW N-SUBSTITUTED AMIDES AND ESTERAAMIDES OF PHOSPHORIC ACID OF THE FORMULA I:
O WHEREIN R1 IS A LOWER ALKYL GROUP HAVING FROM 1 TO 4 CARBON ATOMS BEING SUBSTITUTED WITH ONE OR SEVERAL HALOGEN ATOMS, Z IS HYDROGEN OR A LOWER ALKYL GROUP HAVING FROM 1 TO 4 CARBON ATOMS, M IS 2 OR 3 AND X2 IS THE ETHYLENE IMINO GROUP OR THE GROUP HAVING THE FORMULA:
CL-(-C(-Z)2)M-N-R
WHEREIN R IS HYDROGEN OR A LOWER ALKYL GROUP HAVING FROM 1 TO 4 CARBON ATOMS WHICH MAY BE SUBSTITUTED WITH A CHLORINE ATOM OR A HYDROXY GROUP, AND Z AND M HAVE THE ABOVE-GIVEN MEANING. EACH OF THESE PRODUCTS IS USEFUL AS A CYTOSTATICALLY EFFECTIVE COMPOUND AND IS USED IN THE MANNER EXEMPLIFIED HEREINAFTER WITH RESPECT TO TEST ANIMALS, E.G. RATS, ACCORDING TO KNOWN TECHNIQUES FOR ADMINISTERING TEST DOSAGES.
摘要:
The present invention is related to certain new basic Alpha nortricyclyl-(3)-benzyl ethers and salts, quaternary ammonium salts and N-oxides thereof, pharmaceutical composition comprising the same as active principle and a process for the treatment of spasm.