Soluble azole antifungal salt
    1.
    发明授权
    Soluble azole antifungal salt 失效
    可溶性唑类抗真菌盐

    公开(公告)号:US5883097A

    公开(公告)日:1999-03-16

    申请号:US61502

    申请日:1998-04-16

    摘要: The lactic acid�CH.sub.3 CH(OH)CO.sub.2 H! addition salt of the compound of formula I ##STR1## wherein the molar ratio of lactic acid, preferably L-lactic acid, to the compound of formula I is preferably about 1:1, pharmaceutical compositions of the lactic acid addition salt in an aqueous lactic acid carrier suitable for intravenous administration, and methods of using either of them to treat and/or prevent susceptible fungal infections in a host such as a mammal are disclosed.

    摘要翻译: 式I化合物的乳酸[CH 3 CH(OH)CO 2 H]加成盐,其中乳酸,优选L-乳酸与式I化合物的摩尔比优选为约1: 1,公开了适用于静脉内给药的乳酸载体的乳酸加成盐的药物组合物,以及使用它们之一来治疗和/或预防哺乳动物宿主易感真菌感染的方法。

    5′-amino acid esters of ribavirin and the use of same to treat hepatitis C with interferon
    7.
    发明授权
    5′-amino acid esters of ribavirin and the use of same to treat hepatitis C with interferon 失效
    利巴韦林的5'-氨基酸酯及其用途用干扰素治疗丙型肝炎

    公开(公告)号:US06277830B1

    公开(公告)日:2001-08-21

    申请号:US09348534

    申请日:1999-07-07

    IPC分类号: A01N4304

    CPC分类号: C07H19/056 Y10S514/894

    摘要: 5′-Amino acid esters of ribavirin represented by formula I: wherein R is CH3CH(NH2)—CO—, CH3CH2(CH3)CHCH(NH2)—CO—or H2N(CH2)4CH(NH2)—CO—; preferably R is or a pharmaceutically acceptable salt thereof, e.g., trifluoroacetate, tosylate, mesylate, and chloride, pharmaceutical compositions containing them as well as methods of treating patients having susceptible viral infections, e.g., chronic hepatitis C infections by administering a therapeutically effective amount of a ribavirin derivative, alone or in combination with a therapeutically effective amount of interferon-alpha are disclosed.

    摘要翻译: 由式I表示的利巴韦林的氨基酸酯:其中R是CH 3 CH(NH 2)-CO-,CH 3 CH 2(CH 3)CHCH(NH 2)-CO-或H 2 N(CH 2)4 CH(NH 2)-CO-; 优选R是其药学上可接受的盐,例如三氟乙酸盐,甲苯磺酸盐,甲磺酸盐和氯化物,含有它们的药物组合物以及治疗患有易感病毒感染的患者的方法,例如慢性丙型肝炎感染,通过施用治疗有效量的 公开了单独或与治​​疗有效量的干扰素-α组合的利巴韦林衍生物。

    Hydroxy-substituted antifungals
    8.
    发明授权
    Hydroxy-substituted antifungals 失效
    羟基取代的抗真菌剂

    公开(公告)号:US5698557A

    公开(公告)日:1997-12-16

    申请号:US664758

    申请日:1996-06-17

    CPC分类号: C07F9/65181 C07F9/65583

    摘要: A compound represented by the formula I ##STR1## wherein X is independently both F or both Cl or one X is independently F and the other is independently Cl; R.sub.1 is a straight or branched chain (C.sub.3 to C.sub.8) alkyl group substituted by one or two hydroxy moieties, an ether or ester thereof (e.g., a polyether ester, heterocyclic ester amino acid ester or phosphate ester) thereof and the carbon with the asterisk (*) has the R or S absolute configuration or a pharmaceutically acceptable salt thereof and pharmaceutical compositions thereof useful for treating and/or preventing fungal infections are disclosed.

    摘要翻译: 由式I表示的化合物其中X独立地为F或两者为Cl或一个X独立地为F,另一个独立地为Cl; R1是被一个或两个羟基部分取代的直链或支链(C3至C8)烷基,其醚或酯(例如,聚醚酯,杂环酯氨基酸酯或磷酸酯)和具有星号的碳 (*)具有R或S绝对构型或其药学上可接受的盐和用于治疗和/或预防真菌感染的药物组合物。