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    • 5. 发明授权
    • 14.beta.-H-, 14-and 15-En-11.beta.-aryl-4-oestrenes
    • 14β-H,14和15-En-11β-芳基-4-盎司
    • US5426102A
    • 1995-06-20
    • US81269
    • 1993-06-22
    • Wolfgang SchwedeEckhard OttowGunter NeefArwed CleveKrzysztof ChwaliszHorst Michna
    • Wolfgang SchwedeEckhard OttowGunter NeefArwed CleveKrzysztof ChwaliszHorst Michna
    • A61K31/57A61K31/58A61K31/585A61P5/38C07J1/00C07J3/00C07J5/00C07J7/00C07J9/00C07J17/00C07J21/00C07J33/00C07J41/00C07J43/00
    • C07J1/0092C07J1/0088C07J1/0096C07J17/00C07J33/002C07J41/0094C07J43/003C07J9/00
    • Novel compounds of the general formula I ##STR1## and the pharmacologically tolerable addition salts thereof with acids are described, in which eitherIa) R.sup.11 represents a hydrogen atom in the .beta.-configuration and each of R.sup.12 and R.sup.13 represents a hydrogen atom, orIb) R.sup.11 represents a hydrogen atom in the .beta.-configuration and R.sup.12 and R.sup.13 together represent a second bond, orIc) R.sup.11 and R.sup.12 together represent a second bond and R.sup.13 represents a hydrogen atom, orId) R.sup.11 represents a hydrogen atom in the .alpha.-configuration and R.sup.12 and R.sup.13 together represent a second bond,and in Ia), Ib), Ic) or Id)X represents an oxygen atom, the hydroxyimino grouping >N.about.OH or two hydrogen atoms,R.sup.1 represents a hydrogen atom or a methyl group,R.sup.2 represents a hydroxy group, a C.sub.1 -C.sub.10 -alkoxy group or a C.sub.1 -C.sub.10 -acyloxy group, andR.sup.3 and R.sup.4 have the meanings customary for competitive progesterone antagonists specified in the description.The invention relates also to processes for the preparation of the novel compounds, to pharmaceutical compositions containing those compounds, to their use for the manufacture of medicaments, and to the novel intermediates required for the process.The novel compounds have a strong affinity for the gestagen receptor and exhibit pronounced antigestagenic and also antiglucocorticoid, antimineralocorticoid and antiandrogenic properties.
    • PCT No.PCT / EP91 / 02494 371日期:1993年6月22日 102(e)日期1993年11月1日PCT 1991年12月21日PCT PCT。 出版物WO92 / 11278 描述了通式I的新型化合物(Ⅰ)及其与酸的药理学上可以忍受的加成盐,其中Ia)R11表示β-构型中的氢原子, R 12和R 13表示氢原子,或Ib)R 11表示β构型中的氢原子,R 12和R 13一起表示第二键,或者Ic)R 11和R 12一起表示第二键,R 13表示氢原子,或 Id)R11表示α-构型中的氢原子,R 12和R 13一起表示第二键,并且在Ia),Ib),Ic)或Id)中X表示氧原子,羟基亚氨基> N不同OH或两个 氢原子,R 1表示氢原子或甲基,R 2表示羟基,C 1 -C 10 - 烷氧基或C 1 -C 10 - 酰氧基,R 3和R 4具有常规用于在 描述。 本发明还涉及制备新化合物的方法,含有这些化合物的药物组合物,其用于制备药物的方法以及该方法所需的新型中间体。 新化合物对于孕激素受体具有强烈的亲和力,并且具有显着的抗原成分和抗糖皮质激素,抗皮质激素和抗雄激素的特性。
    • 8. 发明授权
    • 19,11 .beta.-bridged steroids, their manufacture and pharmaceutical
preparations containing them
    • 19,11(BETA) - 混合型STEROIDS,其制造和含有它们的药物制剂
    • US5095129A
    • 1992-03-10
    • US283632
    • 1988-12-09
    • Eckhard OttowRudolf WiechertGunter NeefSybille BeierWalter ElgerDavid A. Henderson
    • Eckhard OttowRudolf WiechertGunter NeefSybille BeierWalter ElgerDavid A. Henderson
    • A61K31/565A61K31/58A61P5/00C07J21/00C07J31/00C07J41/00C07J53/00C07J63/00C07J71/00
    • C07J71/0063C07J21/006C07J31/006C07J41/0038C07J53/002C07J71/0005C07J71/0047
    • New 19,11.beta.-bridged steroids of the general formula I ##STR1## where R.sup.1 stands for a methyl or ethyl radical,R.sup.2 for a hydrogen or chlorine atom or a C.sub.1 -C.sub.4 -alkyl radical,B and G, which are the same or different, respectively for a hydrogen atom, a C.sub.1 -C.sub.4 -alkyl radical or, together, for a second bond between the carbon atoms 6 and 7,B and R.sup.2 together for a methylene or an ethylene group,Z for the radical of a pentagonal or hexagonal ring, which is possibly substituted and possibly unsaturated,V stands for a possibly substituted carbocyclic or heterocyclic aryl radical,the ring A for ##STR2## M and N together meaning a second bond or M a hydrogen atom and N a hydroxy group,X means an oxygen atom, two hydrogen atoms or a hydroxyimino grouping N.about.OH,R.sup.3 and D, which are the same or different, respectively a hydrogen atom, a nitrile radical or a C.sub.1 -C.sub.4 -alkyl radical or, together, a methylene or ethylene group,E a hydrogen atom or a C.sub.1 -C.sub.4 -alkyl radical,D and E together meaning a second bond between carbon atoms 1 and 2 or together a methylene group ##STR3## with R.sup.11 in the meaning of a hydrogen atom or a C.sub.1 -C.sub.8 -alkyl radical,are described as well as their pharmaceutically tolerated addition salts with acids. The new compounds possess valuable pharmacological properties.
    • 新的19,11个β-桥连类固醇,其通式为Ⅰ(Ⅰ),其中R1代表甲基或乙基,R2代表氢或氯原子或C1-C4烷基,B和G,其中 分别对于氢原子,C 1 -C 4 - 烷基或碳原子6和7之间的第二个键,B和R 2一起为亚甲基或亚乙基,Z为相同或不同的 可能被取代且可能不饱和的五角或六方环的基团V代表可能被取代的碳环或杂环芳基,A,A,M和N一起表示第二个键或M是氢原子 和N是羟基,X表示氧原子,两个氢原子或羟基亚氨基基团N分别OH,R3和D分别相同或不同,分别为氢原子,腈基或C1-C4烷基 或者一起是亚甲基或亚乙基,E是氢原子或C 1 -C 4烷基,D和E togeth 呃意指碳原子1和2之间的第二个键或一起与氢原子或C 1 -C 8 - 烷基的含义中的R 11一起形成的亚甲基基团b)或者c),以及 它们与酸的药学上耐受的加成盐。 新化合物具有宝贵的药理性质。