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    • 12. 发明授权
    • Composition and method of producing infertility in male rodents
    • 雄性啮齿类动物不育症的组成和方法
    • US4012520A
    • 1977-03-15
    • US601487
    • 1975-08-04
    • Gilbert A. Youngdale
    • Gilbert A. Youngdale
    • A01N43/28A01N9/12
    • A01N43/28
    • Pharmaceutical preparations in dosage forms and animal feeds (baits) consisting essentially of pharmaceutically acceptable carriers, oral and injectable, compounded with a sublethal, yet effective, amount of a compound having the formula: ##STR1## and R.sub.1 and R.sub.2 are the same or different and are hydrogen, alkyl of from 1 to 17 carbon atoms, alkenyl of from 2 to 17 carbon atoms, phenyl, a heterocyclic ring such as furyl, pyrrolyl, thienyl, indolyl or pyridyl, and R.sub.1 and R.sub.2, taken together, can be a carbocyclic ring of up to 8 carbon atoms, for inducing sterility in male mammals. Methods for preventing impregnation of females by male mammals which comprises administering systemically to male mammals a sterilizing amount of a compound of the Formula l.
    • 基本上由药学上可接受的载体组成的剂型和动物饲料(诱饵)的药物制剂,口服和可注射的,与亚致死但有效量的具有下式的化合物:其中R 1和R 2相同 或不同的是氢,1至17个碳原子的烷基,2至17个碳原子的烯基,苯基,杂环如呋喃基,吡咯基,噻吩基,吲哚基或吡啶基,以及R1和R2一起可以 是最多8个碳原子的碳环,用于在雄性哺乳动物中诱导不育。 用于防止雄性哺乳动物浸渍雌性的方法,其包括向雄性哺乳动物全身施用灭菌量的式I化合物。
    • 15. 发明授权
    • Cyclic hydrocarbons with an aminoalkyl sidechain
    • 具有氨基烷基侧链的环状烃
    • US5001234A
    • 1991-03-19
    • US435481
    • 1989-10-16
    • Gordon L. BundyGilbert A. Youngdale
    • Gordon L. BundyGilbert A. Youngdale
    • C07J41/00C07J51/00
    • C07J41/0072C07J41/0005C07J41/0094C07J51/00
    • This invention provides novel cyclic hydrocarbons of the formula: ##STR1## wherein R is selected from the group consisting of CH.sub.2 .dbd.CH--CH.sub.2 --, HO--CH.sub.2 CH.sub.2 CH.sub.2 --, and CH.sub.3 ;wherein R.sub.1 is selected from the group consisting of m-trifluoromethylphenylmethyl, 2-thienylmethyl, and p-aminosulfonylphenylethyl;wherein R.sub.2 and R.sub.3 are methyl or hydrogen;wherein R.sub.4 is hydrogen or --OH;a compound of the formula ##STR2## wherein R is (CH.sub.3).sub.2 NCH.sub.2 CH.sub.2 CH.sub.2 -- or NH.sub.2 CH.sub.2 CH.sub.2 CH.sub.2 --;or a compound of the formula ##STR3## wherein the dashed line indicates that the 2-3 bond is saturated or unsaturated and, wherein R is hydrogen or methyl.These compounds are useful for inhibiting adverse physiological symptoms associated with phospholipase A.sub.2 and for treating hyperglycemia associated diseases such as diabetes and obesity.
    • PCT No.PCT / US88 / 00978 Sec。 371日期:1989年10月16日 102(e)日期1989年10月16日PCT提交1988年4月1日PCT公布。 出版物WO88 / 08002 本发明提供了下式的新型环状烃:其中R选自CH 2 = CH-CH 2 - ,HO-CH 2 CH 2 CH 2 - 和CH 3; 其中R1选自间三氟甲基苯甲基,2-噻吩基甲基和对氨基磺酰基苯乙基; 其中R2和R3是甲基或氢; 其中R4是氢或-OH; 其中R为(CH 3)2 NHCH 2 CH 2 CH 2 - 或NH 2 CH 2 CH 2 CH 2 - 的式 或式“IMAGE”的化合物,其中虚线表示2-3键是饱和或不饱和的,其中R是氢或甲基。 这些化合物可用于抑制与磷脂酶A2相关的不良生理学症状和用于治疗高血糖症相关疾病如糖尿病和肥胖症。