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1.
Pharmazie ; 33(4): 190-1, 1978 Apr.
Article in English | MEDLINE | ID: mdl-674310

ABSTRACT

The synthesis of 5,5'-Bis[4-(N-mono and disubstituted aminoethylamino)-naphthylazo]-2.2'-dipyridyldisulphides has been achieved by the coupling of 2.2'-dipyridyldisulphide-5.5'-tetrazonium chloride with different N-mono and N.N-disubstituted N'-1-naphthylethylenediamines.


Subject(s)
Azo Compounds/chemical synthesis , Naphthalenes/chemical synthesis , Schistosomicides/chemical synthesis , Azo Compounds/analysis , Disulfides/analysis , Disulfides/chemical synthesis , Methods , Naphthalenes/analysis
3.
Pharmazie ; 31(11): 774-5, 1976 Nov.
Article in English | MEDLINE | ID: mdl-1023241

ABSTRACT

Seven new 3.5-dioxopyrazolidine derivatives, incorporating in their molecule a p-substituted benzoyl grouping, were synthesized. The preliminary screening of four selected compounds showed that 1-phenyl-2-[p-nitrobenzoyl]-4.4-diethyl-3.5-dioxopyrazolidine possesses a low order of antiinflammatory activity.


Subject(s)
Anti-Inflammatory Agents , Pyrazoles , Animals , Anti-Inflammatory Agents/chemical synthesis , Drug Evaluation, Preclinical , Gossypium , Inflammation/chemically induced , Phenylbutazone/pharmacology , Pyrazoles/chemical synthesis , Pyrazoles/pharmacology , Rats
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