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Synthesis, binding affinities for alpha-adrenoceptor and eudismic analysis of chiral benzodioxane derivatives and their chiral opened analogues. 手性苯并二氧杂环衍生物及其手性开放类似物的合成、与肾上腺素受体的结合亲和性及流行病学分析。
Pub Date : 1988-12-01
V Ferri, M Pallavicini, D Piccini, E Valoti, L Villa, N Brunello, G Racagni
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引用次数: 0
Prolyl derivatives of enalapril as potential angiotensin converting enzyme inhibitors. 依那普利脯氨酸衍生物作为潜在的血管紧张素转换酶抑制剂。
Pub Date : 1988-12-01
R Ciabatti, G Tarzia, F Battaglia, D Barone, E Baldoli

The synthesis of a new class of potential angiotensin converting enzyme (ACE) inhibitors, analogs of enalapril, is reported. In these molecules the C-terminal amino acidic sequence Ala-Pro of enalapril was replaced by the sequence Pro-Pro. The compounds were tested both in vitro and in vivo. They showed no in vivo activity but only a week in vitro inhibitory activity.

报道了一类新的血管紧张素转换酶(ACE)抑制剂——依那普利类似物的合成。在这些分子中,依那普利的c端氨基酸序列Ala-Pro被Pro-Pro序列取代。在体外和体内对这些化合物进行了测试。它们在体内没有活性,但只有一周的体外抑制活性。
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引用次数: 0
Amidinosemicarbazido derivatives of pyrazole: synthesis and inhibitory effect on blood coagulation and platelet aggregation. 吡唑氨基氨基脲基衍生物的合成及其对凝血和血小板聚集的抑制作用。
Pub Date : 1988-11-01 DOI: 10.1002/CHIN.198923166
R. Ferroni, L. Milani, D. Simoni, P. Orlandini, T. Poli, M. Guarneri, U. Taddeo
Amidinosemicarbazido derivatives of pyrazole having various substituents on pyrazole ring were prepared and their effect on platelet function and blood coagulation was determined in vitro. Platelet aggregation and serotonin release induced by ADP, collagen, arachidonic acid and thrombin were markedly inhibited by pyrazole derivatives at mM concentrations. Compounds with a hydrophobic nucleus at position 1 of the pyrazole ring showed the most potent antiplatelet activity. On the contrary, their effect on blood coagulation was faintly inhibitory.
制备了吡唑环上具有不同取代基的氨基氨基脲基吡唑衍生物,并测定了其体外对血小板功能和凝血功能的影响。吡唑衍生物在mM浓度下显著抑制ADP、胶原、花生四烯酸和凝血酶诱导的血小板聚集和血清素释放。在吡唑环1号位置具有疏水核的化合物显示出最有效的抗血小板活性。相反,它们对凝血的抑制作用微弱。
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引用次数: 0
Amidinosemicarbazido derivatives of pyrazole: synthesis and inhibitory effect on blood coagulation and platelet aggregation. 吡唑氨基氨基脲基衍生物的合成及其对凝血和血小板聚集的抑制作用。
Pub Date : 1988-11-01
R Ferroni, L Milani, D Simoni, P Orlandini, T Poli, M Guarneri, U Taddeo

Amidinosemicarbazido derivatives of pyrazole having various substituents on pyrazole ring were prepared and their effect on platelet function and blood coagulation was determined in vitro. Platelet aggregation and serotonin release induced by ADP, collagen, arachidonic acid and thrombin were markedly inhibited by pyrazole derivatives at mM concentrations. Compounds with a hydrophobic nucleus at position 1 of the pyrazole ring showed the most potent antiplatelet activity. On the contrary, their effect on blood coagulation was faintly inhibitory.

制备了吡唑环上具有不同取代基的氨基氨基脲基吡唑衍生物,并测定了其体外对血小板功能和凝血功能的影响。吡唑衍生物在mM浓度下显著抑制ADP、胶原、花生四烯酸和凝血酶诱导的血小板聚集和血清素释放。在吡唑环1号位置具有疏水核的化合物显示出最有效的抗血小板活性。相反,它们对凝血的抑制作用微弱。
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引用次数: 0
Benzodiazepine receptor ligands. Synthesis and pharmacological evaluation of 6-aryl-3,8-disubstituted-1,2,4-triazolo[3,4-a]phthalazines. 苯二氮卓类受体配体。6-芳基-3,8-二取代-1,2,4-三唑[3,4-a]酞嗪的合成及药理评价。
Pub Date : 1988-11-01 DOI: 10.1002/chin.198923193
G. Tarzia, E. Occelli, D. Barone
A series of 6-aryl-3,8-disubstituted-1,2,4-triazolo[3,4-a]phthalazines was synthesised starting from suitable o-benzoylbenzoic acids. The compounds were tested in vitro for inhibition of the specific binding of 3H-Diazepam to benzodiazepine receptors in preparations of membranes from rat brain synaptosomes. None of the compounds was notably active in this test.
以合适的邻苯甲酰苯甲酸为起始原料,合成了一系列6-芳基-3,8-二取代-1,2,4-三唑[3,4- A]邻苯二甲酸。在体外测试了化合物对大鼠脑突触体膜制备中3h -地西泮与苯二氮卓受体特异性结合的抑制作用。在这项试验中,这些化合物都没有明显的活性。
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引用次数: 0
[Synthesis and anti-ulcer activity of some new compounds with arylthiomethyl-pyridine structure]. [一些芳基硫甲基吡啶结构新化合物的合成及其抗溃疡活性]。
Pub Date : 1988-11-01 DOI: 10.1002/CHIN.198923176
S. Evangelista, M. Ghelardoni, A. Meli, V. Pestellini, G. Viti
We report the results of the antiulcer activity of some arylthiomethylpyridine compounds. Some of these showed gastroprotective activity against 96% ethanol-induced gastric lesions greater than Omeprazole. However they possess antiulcer properties lower than the reference compound against Indomethacin-induced gastric ulcers.
我们报告了一些芳基硫甲基吡啶化合物的抗溃疡活性的结果。其中一些药物对96%乙醇性胃病变的胃保护作用强于奥美拉唑。然而,他们具有抗溃疡的性质低于对照化合物对吲哚美辛引起的胃溃疡。
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引用次数: 1
Nonsteroidal antiinflammatory agents. XVIII - Stereomeric optically active halogenophenyl-biphenylyl-hydroxypropionic acids. 非甾体类抗炎药。立体旋光性卤代苯基-联苯基-羟基丙酸。
Pub Date : 1988-11-01
L Varoli, S Burnelli, A Guarnieri, N Ghedini, G Scapini, S Ferri, E Cavicchini

The optically active stereomers of some 3-(fluoro-, chloro-, bromophenyl)-2-biphenylyl-3-hydroxypropionic acids were prepared and tested for antiinflammatory activity. Surprisingly, the four bromo-isomers were the most active ones, particularly in the threo configuration.

制备了几种3-(氟、氯、溴苯基)-2-联苯基-3-羟基丙酸的旋光性对映体,并对其抗炎活性进行了测试。令人惊讶的是,四个溴同分异构体是最活跃的,特别是在三个构型中。
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引用次数: 0
N,N-disubstituted 4-amino-(6-methoxy)-3-phenyl-2H-naphtho [1,2-b]pyran-2-ones with antiarrhythmic, platelet antiaggregating and local anesthetic activities. 具有抗心律失常、抗血小板聚集和局部麻醉活性的N,N-二取代4-氨基-(6-甲氧基)-3-苯基- 2h -萘[1,2-b]吡喃-2- 1。
Pub Date : 1988-11-01 DOI: 10.1002/chin.198923181
A. Bargagna, M. Longobardi, E. Mariani, P. Schenone, S. Russo, S. Vilagliano, V. de Novellis, E. Marmo
The synthesis of title compounds (VI) by 1,4-cycloaddition of phenylchloroketene to N,N-disubstituted (E)-2-aminomethylene-3,4-dihydro-(6-methoxy)-1(2H)naphthalenones, followed by dehydrochlorination with DBN and dehydrogenation with Pd/C of the resulting cycloadducts, is described. Some compounds (VI) showed antiarrhythmic activity in rats higher or like that of quinidine and platelet antiaggregating activity in vitro like that of acetylsalycilic acid, as well as moderate infiltration anesthesia in mice and weak hypotensive, bradicardic and antiinflammatory activities in rats.
用1,4-苯基氯烯酮与N,N-二取代(E)-2-氨基甲基-3,4-二氢-(6-甲氧基)-1(2H)萘酮加成,然后用DBN脱氢氯化,再用Pd/C脱氢,合成了标题化合物(VI)。部分化合物(VI)在大鼠体内的抗心律失常活性高于或接近奎尼丁,体外抗血小板聚集活性类似于乙酰水杨酸,在小鼠体内具有中度浸润麻醉作用,在大鼠体内具有较弱的降压、心动缓和抗炎作用。
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引用次数: 2
Aminoethers of 1,3,3-trimethyl-5-(phenylmethylene)-2-oxabicyclo[2.2.2]octan-6-h ydroxy imine with antiarrhythmic activity. 具有抗心律失常活性的1,3,3-三甲基-5-(苯基亚甲基)-2-氧沙比环辛烷-6-h羟基亚胺的氨基醚。
Pub Date : 1988-11-01
E Mariani, A Bargagna, M Longobardi, P Schenone, S Russo, W Filippelli, L Molinario, E Marmo

The synthesis of beta-dialkylaminoethyl ethers (III a-f) and gamma-dialkylaminopropyl ethers (III g-l) starting from 1,3,3-trimethyl-5-(phenylmethylene)-2-oxabicyclo[2.2.2]octan-6- hydroxyimine (II) is described. beta-Diisopropylaminoethyl ether (III b) and gamma-piperidinopropyl ether (III i) showed an antiarrhythmic activity in rats similar to that of quinidine. Moreover, a number of ethers (III) showed weak hypotensive and bradycardic activity in rats and moderate infiltration anesthesia in mice.

以1,3,3-三甲基-5-(苯基亚甲基)-2-氧沙比环辛烷-6-羟亚胺(II)为起始原料,合成了-二烷基氨基乙醚(III a-f)和-二烷基氨基丙基醚(III g-l)。-二异丙基氨基乙醚(III b)和-哌啶丙基醚(III i)在大鼠中显示出与奎尼丁相似的抗心律失常活性。此外,一些醚(III)在大鼠中表现出微弱的降压和心动过缓活动,在小鼠中表现出中度浸润麻醉。
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引用次数: 0
[New heterocyclic derivatives of benzimidazole with germicidal activity. V. Synthesis and activity of new derivatives of di-2-benzimidazolyl-2,5-furan]. 新的具有杀菌活性的苯并咪唑杂环衍生物。二-2-苯并咪唑-2,5-呋喃新衍生物的合成及活性研究[j]。
Pub Date : 1988-11-01
M Pedini, G Alunni Bistocchi, G De Meo, A Ricci, L Bastianini, T Sposini, P Jacquignon

In continuation of the research in the field of germicidal and antimycotic agents, the synthesis of 14 new derivatives of di-2-benzimidazolyl-2,5-furan is described. These derivatives are differently substituted (R not equal to R') in the position 5 of the two benzene rings. These new compounds showed no germicidal or fungicidal activity, when tested on different cultures. New compounds are under investigation.

在抗菌药物研究的基础上,合成了14个新的二-2-苯并咪唑-2,5-呋喃衍生物。这两个衍生物在两个苯环的5号位置上被不同地取代(R不等于R')。这些新化合物在不同的培养物上没有杀菌或杀真菌活性。新的化合物正在研究中。
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引用次数: 0
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Il Farmaco; edizione scientifica
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