摘要:
Purine derivatives represented by general formula (I) or salts thereof, useful as the active ingredient of medicines such as antasthmatic, wherein R1 represents C¿1?-C4 alkyl or difluoromethyl; R?2¿ represents tetrahydrofuranyl, C¿1?-C7 alkyl, etc.; X represents hydrogen, halogeno or nitro; and A represents a group represented by general formula (II) or (III), wherein R?3¿ represents hydrogen, halogeno, etc.; and R?4 and R5¿ represent each hydrogen, halogeno, C¿1?-C4 alkyl, C1-C4 alkoxy, etc.
摘要:
New heterocyclic derivatives of formula (1) based on N6-substituted adenine, having anticancer, mitotic, imunosuppressive and antisenescent propoerties for plant, animal and human cells and methods of their preparation. Included are also pharmaceutical compositions, cosmetic preparations and growth regulators, which contain these derivatives as active compound and the use of these derivatives for the preparation of drugs, cosmetic preparations, in biotechnological processes, in cosmetics and in agriculture.
摘要:
Disclosed are processes for preparing compounds of formula (I) and pharmaceutically acceptable salts or esters thereof, wherein R2 is a purine or pyrimidine base or an analogue or derivative thereof; and Z is S, S = O or SO2. The invention also relates to intermediates of use in the preparation of these compounds.
摘要:
Compounds of formula (I) are HIV protease inhibitors. These compounds are useful in the prevention or treatment of infection by HIV and in the treatment of AIDS, either as compounds, pharmaceutically acceptable salts, pharmaceutical composition ingredients, whether or not in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of treating AIDS and methods of preventing or treating infection by HIV are also described.
摘要:
A method and composition for the treatment of humans infected with HIV that includes the administration of an HIV treatment amount of an enantiomerically pure β-D-dioxolanyl purine nucleoside of formula (I), wherein R is OH, Cl, NH2, or H, or a pharmaceutically acceptable salt or derivative of the compound, optionally in a pharmaceutically acceptable carrier or diluent.
摘要:
A process for the preparation of an amino acid ester of a nucleoside analogue, said process comprising reacting a nucleoside analogue having an esterifiable hydroxy group in its linear or cyclic ether moiety with a 2-oxa-4-aza-cycloalkane-1,3-dione, which process is economical, quick and simple to perform.