Quinolone compounds for the treatment of disorders caused by
helicobacter pylori
    2.
    发明授权
    Quinolone compounds for the treatment of disorders caused by helicobacter pylori 失效
    喹诺酮化合物用于治疗由幽门螺杆菌引起的疾病

    公开(公告)号:US5942619A

    公开(公告)日:1999-08-24

    申请号:US43374

    申请日:1998-04-24

    摘要: This invention provides processes for producing quinolone compounds which comprise cultivating Amycoa sp. FERM BP-4785, and then isolating quinolone compounds from the fermentation broth. The compounds produced by these processes include compounds of formula (I) wherein R.sup.1 is H, R.sup.2 is (a) and R.sup.3 is CH.sub.3 ; R.sup.1 is CH.sub.3, R.sup.2 is (a) and R.sup.3 is CH.sub.3 ; or R.sup.1 is CH.sub.3, R.sup.2 is (b) and R.sup.3 is CH.sub.3 ; and the like. The present invention also relates to a pharmaceutical composition comprising the same, which is useful in the treatment of diseases, disorders and adverse conditions caused by Helicobacter pylori and is particularly useful in the treatment of gastroduodenal disorders, diseases and adverse conditions caused thereby. ##STR1##

    摘要翻译: PCT No.PCT / IB96 / 00670 Sec。 371日期:1998年4月24日 102(e)1998年4月24日PCT PCT 1996年7月11日PCT公布。 出版物WO97 / 12868 日期:1997年04月10日本发明提供了生产喹诺酮化合物的方法,其中包括培养Amycoa sp。 FERM BP-4785,然后从发酵液中分离出喹诺酮化合物。 通过这些方法制备的化合物包括其中R 1是H,R 2是(a)和R 3是CH 3的式(I)化合物; R1是CH3,R2是(a),R3是CH3; 或R 1为CH 3,R 2为(b),R 3为CH 3; 等等。 本发明还涉及含有该组合物的药物组合物,其可用于治疗由幽门螺杆菌引起的疾病,病症和不利条件,并且特别可用于治疗胃十二指肠疾病,疾病和由此引起的不利条件。

    Compounds for treating gastroduodenal diseases
    3.
    发明授权
    Compounds for treating gastroduodenal diseases 失效
    用于治疗胃十二指肠疾病的化合物

    公开(公告)号:US06372781B1

    公开(公告)日:2002-04-16

    申请号:US09588889

    申请日:2000-06-07

    IPC分类号: A61K31365

    CPC分类号: C07D493/10

    摘要: Spirolaxine, the compound of formula (I) wherein R is H, and the novel compounds of formula (I) wherein R is (C1-C5) alkyl or CH3(CH2)nCO and n is 1, 2, 3 or 4 are useful in treating gastroduodenal diseases such as gastric ulcers, duodenal ulcers and gastric cancer caused by Helicobacter pylori. Spirolaxine and spirolaxine methyl ether are isolated from the fermentation of Sporotrichum pruinosum ATCC 74278. Spirolaxine and the compounds of formula (I) are also useful in combination with H2 antagonist, colloidal bismuth subcitrate and other antibiotics.

    摘要翻译: 其中R为H的式(I)化合物和其中R为(C 1 -C 5)烷基或CH 3(CH 2)n CO且n为1,2,3或4的式(I)的新型化合物的Spirolaxine为有用的 用于治疗由幽门螺杆菌引起的胃十二指肠疾病如胃溃疡,十二指肠溃疡和胃癌。 Spirolaxine和spirolaxine甲醚从Sporotrichum pruinosum ATCC 74278的发酵中分离。Spirolaxine和式(I)化合物也可与H2拮抗剂,胶体铋亚硝酸盐和其他抗生素组合使用。

    Spirolaxine derivatives for treating gastrobuodenal diseases
    4.
    发明授权
    Spirolaxine derivatives for treating gastrobuodenal diseases 失效
    用于治疗胃十二指肠疾病的Spirolaxine衍生物

    公开(公告)号:US06174710B1

    公开(公告)日:2001-01-16

    申请号:US08765437

    申请日:1997-01-16

    IPC分类号: A61K31365

    CPC分类号: C07D493/10

    摘要: Spirolaxine, the compound of formula (I) wherein R is H, and the novel compounds of formula (I) wherein R is (C1-C6)alkyl or CH3(CH2)nCO and n is 1, 2, 3 or 4 are useful in treating gastroduodenal diseases such as gastric ulcers, duodenal ulcers and gastric cancer caused by Helicobacter pylori. Spirolaxine and spirolaxine methyl ether are isolated from the fermentation of Sporotrichum pruinosum ATCC 74278. Spirolaxine and the compounds of formula (I) are also useful in combination with H2 antagonist colloidal bismuth subcitrate and other antibiotics.

    摘要翻译: 其中R为H的式(I)化合物和其中R为(C 1 -C 6)烷基或CH 3(CH 2)n CO且n为1,2,3或4的式(I)的新化合物的Spirolaxine是有用的 用于治疗由幽门螺杆菌引起的胃十二指肠疾病如胃溃疡,十二指肠溃疡和胃癌。 Sporrolaxine和Spirolaxine甲醚从Sporotrichum pruinosum ATCC 74278的发酵中分离出来。Spirolaxine和式(I)化合物也可与H2拮抗剂胶体铋亚硝酸盐和其他抗生素组合使用。

    Process for preparing spirolaxine and spirolaxine methyl ether
    5.
    发明授权
    Process for preparing spirolaxine and spirolaxine methyl ether 失效
    制备spirolaxine和spirolaxine甲基醚的方法

    公开(公告)号:US6074855A

    公开(公告)日:2000-06-13

    申请号:US894088

    申请日:1997-08-14

    CPC分类号: C12P17/181

    摘要: Processes for preparing spirolaxine and spirolaxine methyl ether, the compounds of formulas (I) and (II) respectively, ##STR1## comprising fermenting fungi selected from the group consisting of Sporotrichum pruinosum FD 29585, ATCC 74327; Sporotrichum pruinosum FD 29454, ATCC 74329; Sporotrichun pruinosum FD 29586, ATCC 74328; and Phanerochaete chrysosporiun LN 3576, ATCC 74326. This invention also relates to a process for preparing spirolaxine comprising fermenting Sporotrichum pruinosum FD 29458, ATCC 74330.

    摘要翻译: PCT No.PCT / IB95 / 00217 Sec。 371日期1997年8月13日 102(e)日期1997年8月13日PCT 1995年3月30日PCT公布。 出版物WO96 / 30538 日期1996年10月3日分别制备螺旋石和螺旋甲醚的方法,分别为式(I)和(II)的化合物,其包含发酵真菌,其选自Sporotrichum pruinosum FD 29585,ATCC 74327; Sporotrichum pruinosum FD 29454,ATCC 74329; Sporotrichun pruinosum FD 29586,ATCC 74328; 和Phanerochaete chrysosporiun LN 3576,ATCC 74326.本发明还涉及一种制备Spirolaxine的方法,其包括发酵Sporotrichum pruinosum FD 29458,ATCC 74330。