首页> 外国专利> (N-phosphonoacetyl-L-aspartato) (1,2 diaminocyclohexane) platinum (II) and the sodium, potassium or lithium salts thereof, their preparation and pharmaceutical compositions containing them

(N-phosphonoacetyl-L-aspartato) (1,2 diaminocyclohexane) platinum (II) and the sodium, potassium or lithium salts thereof, their preparation and pharmaceutical compositions containing them

机译:(N-膦酰基乙酰基-L-天冬氨酸)(1,2,二氨基环己烷)铂(II)及其钠盐,钾盐或锂盐,其制备方法和含有它们的药物组合物

摘要

where X is Na+, K+, Li+ or H. (N-phosphonacetyl-L-aspartato) (1,2-diaminocyclohexane)platinum(II) or alkali metal salt thereof has shown antitumor activity in animals such as activity against murine leukemia L1210. Additionally, this agent is used against B-16 and Colon 38 tumors and also Ehrlich ascites tumor. It is effective in dosages of 5-60 mg/kg of body weight and is potentiated in a treatment with cyclophosphamide (CY) (50 mg/kg of body weight) to which may be added hydroxyurea (HU) (1,000-1,500 mg/kg of body weight).;In binary treatment with cis-dichlorodiamineplati- num(II) (or cisplatin) the preferred ratio of the present compound to cisplatin is about 10:1 with a range of about 10:1 to 1 : 10 in mg/kg of body weight.;As to the variations in the formula on the left hand side of the formula, it may be varied as monodentate, such as cisplatin containing a single amine group proceeding from the ring, or bidentate, such as the present compound. The saturated cyclo ring may be C4 or CS-C7 in addition to the present cyclohexane.;The present platinum compound may be prepared by reacting the known L-aspartic acid, N-(phosphonacetyl-) disodium salt (PALA; NSC-224131), with dinitrato(1,2-diaminocyclohexane)platinum(II) (NSC-239851). This compound N-phosphonacetyl-L-aspartato (1,2-diaminocyclohexane)platinum(II) may be combined in multiple drug regimen with substantially improved yield cures over the parent compounds. For example, the compound denoted Pt-268 may be combined in a dual regimen with cyclophosphamide (CY), hydroxyurea (HU), and cisplatin.
机译:其中X是Na + ,K + ,Li + 或H。(N-膦酰基乙酰基-L-天冬氨酸)(1,2-二氨基环己烷铂(II)或其碱金属盐在动物中显示出抗肿瘤活性,例如抗鼠白血病L1210的活性。另外,该试剂还用于抗B-16和结肠38肿瘤以及艾氏腹水肿瘤。它的有效剂量为5-60 mg / kg体重,并在环磷酰胺(CY)(50 mg / kg体重)的治疗中得到加强,可向其中加入羟基脲(HU)(1,000-1,500 mg / kg)在用顺-二氯二胺铂(II)(或顺铂)进行二元处理时,本发明化合物与顺铂的优选比例为约10:1,范围为约10:1至1:10 in (mg / kg体重)。至于配方左侧的配方变化,可以单齿变化,例如从环开始含有单个胺基的顺铂,或双齿,例如本化合物。除了本发明的环己烷以外,饱和的环可以是C 4 或C S -C 7 。使已知的L-天冬氨酸N-(膦酰基乙酰基)二钠盐(PALA; NSC-224131)与二硝基(1,2-二氨基环己烷)铂(II)(NSC-239851)反应。该化合物N-膦酰基乙酰基-L-天冬氨酸(1,2-二氨基环己烷)铂(II)可以与多种药物组合使用,与母体化合物相比可以显着提高收率。例如,表示为Pt-268的化合物可以与环磷酰胺(CY),羟基脲(HU)和顺铂双重使用。

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