N-Substituted acrylamides
    2.
    发明授权
    N-Substituted acrylamides 失效
    N-取代的丙烯酰胺

    公开(公告)号:US3878223A

    公开(公告)日:1975-04-15

    申请号:US34062273

    申请日:1973-03-12

    Applicant: ABBOTT LAB

    CPC classification number: C07D231/40 C07D261/14 Y10S514/87

    Abstract: Acrylamides of N-containing heterocyclic moieties that optionally carry a further hetero atom adjacent to the said N and/or methyl substituent(s) on said hetero ring and at least one chlorine atom adjacent to the double bond of the acrylic moiety have been found to have anti-inflammatory properties at reasonably low dosage levels.

    Abstract translation: 已经发现,含氮杂环部分的丙烯酰胺任选地在所述杂环上邻近所述N和/或甲基取代基和与丙烯酸部分的双键相邻的至少一个氯原子携带另外的杂原子, 在相当低的剂量水平下具有抗炎性质。

    Chelocardin derivatives
    3.
    发明授权
    Chelocardin derivatives 失效
    舍卡定衍生物

    公开(公告)号:US3907889A

    公开(公告)日:1975-09-23

    申请号:US37110373

    申请日:1973-06-18

    Applicant: ABBOTT LAB

    CPC classification number: C07C251/72

    Abstract: A number of specific hydrazone derivatives of chelocardin having high antibiotic activity are described. These new derivatives show unusually low toxicity and consequently, a very high therapeutic index as chemotherapeutic agents against gramnegative organisms.

    Abstract translation: 描述了具有高抗生素活性的许多具有特异性的hydraz ard醛腙衍生物。 这些新衍生物显示异常低的毒性,因此作为抗革兰氏阴性生物体的化学治疗剂具有非常高的治疗指数。

    Chelocardin derivatives
    5.
    发明授权

    公开(公告)号:US3910906A

    公开(公告)日:1975-10-07

    申请号:US37110473

    申请日:1973-06-18

    Applicant: ABBOTT LAB

    CPC classification number: C07D295/22

    Abstract: A number of specific hydrazone derivatives of chelocardin having high antibiotic activity are described. These new derivatives show unusually low toxicity and consequently, a very high therapeutic index as chemotherapeutic agents against gramnegative organisms.

    8-fluoro-2-{8 3-(4-fluorophenylanilinopropyl{9 -gamma-carboline
    6.
    发明授权
    8-fluoro-2-{8 3-(4-fluorophenylanilinopropyl{9 -gamma-carboline 失效
    8-氟-2- {8- 3-(4-氟亚苯基]丙酸{9-马来酰胺

    公开(公告)号:US3687961A

    公开(公告)日:1972-08-29

    申请号:US3687961D

    申请日:1971-05-03

    Applicant: ABBOTT LAB

    CPC classification number: C07D471/04

    Abstract: 8-Fluoro-2-(3-(4-fluorophenylanilino)propyl)-1,2,3,4,tetrahydro-5H -pyrido(4,3-b)indole has been found to be a very useful tranquilizer at low dosages when administered to warmblooded animals. The new compound and its non-toxic acid addition salts have an oral ED50 of about 20 mg./kg. and an oral LD50 of 700 mg./kg.

    Abstract translation: 8-氟-2- [3-(4-氟苯基苯胺基)丙基] -1,2,3,4-四氢-5H-吡啶并[4,3-b]吲哚已被发现是非常有用的镇定剂 施用于温血动物时的低剂量。 新化合物及其无毒酸加成盐具有约20mg./kg的口服ED 50。 口服LD50为700mg./kg。

Patent Agency Ranking