摘要:
This invention relates to new RAR selective retinoid agonists of formula (I) wherein the symbols are as defined in the specification to their pharmaceutically acceptable salts, individual isomers or to a racemic or non-racemic mixture; to pharmaceutical compositions containing them, and to methods for their use as therapeutic agents.
摘要:
Compounds of general formula (1) or salts thereof, exhibiting preventive and therapeutic effects against HIV infections wherein R1 is an optionally substituted five- or six-membered ring group; X1 is a free valency or the like; W is a divalent group represented by, e.g., general formula (2) (wherein A and B are each an optionally substituted five- to seven-membered ring; E¿1? and E4 are each optionally substituted carbon or the like; E2 and E3 are each oxygen or the like; and a and b are each a single bond or a double bond); X?2¿ is a divalent group constituting a straight chain moiety; Z1 is a divalent cyclic group or the like; Z2 is a free valency or the like; and R2 is optionally substituted amino or the like.
摘要:
This invention relates to new RAR selective retinoid agonists of formula (I) wherein the symbols are as defined in the specification to their pharmaceutically acceptable salts, individual isomers or to a racemic or non-racemic mixture; to pharmaceutical compositions containing them, and to methods for their use as therapeutic agents.
摘要:
This invention is to provide a compound for antagonizing CCR5, said compound being represented by formula (I), wherein R1 is an optionally substituted phenyl or an optionally substituted thienyl; Y is -CH¿2?-, -S- or -O-; and R?2, R3 and R4¿ are independently an optionally substituted aliphatic hydrocarbon group or an optionally substituted alicyclic heterocyclic ring group, and being effective for the prevention and treatment of infectious disease of HIV.
摘要:
Compounds of Formula (I), and their N-oxides and agriculturally suitable salts, are disclosed which are useful for controlling undesired vegetation wherein Q is Q-1, Q-2, Q-3 or Q-4; and Q, Z, X, R1 through R20, m, n, and r are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula (I) and a method for controlling undesired vegetation which involves contacting the vegetation or its environment with an effective amount of a compound of Formula (I).
R¹ C₇₋₁₀-Alkyl oder C₇₋₁₀-Alkoxy; R² einen Rest der Formeln
R³ Carboxy oder nieder-Alkoxycarbonyl; und n 1, 2 oder 3 darstellt; und Salze von Carbonsäuren der Formel I können als Heilmittel, z.B. zur Behandlung von Autoimmunerkrankungen bzw. Erkrankungen mit stark immunologischen Komponente, wie Psoriasis, Verwendung finden.
摘要翻译:其中X表示-S-,-SO-或-SO 2 - 的式“IMAGE”的化合物; R 1表示C 7-10 - 烷基或C 7-10 - 烷氧基; R 2表示下式的基团,其中R 3表示羧基或低级烷氧基羰基; n表示1,2或3; 并且式I的羧酸的盐可以用作药物,例如, 用于治疗具有强免疫组分(例如银屑病)的自身免疫性疾病或病症。
摘要:
The invention relates to substituted benzo-condensed cycloheptanone derivatives, to methods for producing them, to drugs containing said compounds and to the use of said compounds for producing drugs.
摘要:
Compounds of formula: (I) pharmaceutically acceptable salts, solvates, solvates of such salts and prodrugs thereof and their use as ileal bile acid transport (IBAT) inhibitors for the treatment of hyperlipidaemia are described. Processes for their manufacture and pharmaceutical compositions containing them are also described.