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1.
Farmaco Sci ; 33(2): 118-25, 1978 Feb.
Article in English | MEDLINE | ID: mdl-204511

ABSTRACT

The alpha-adrenolytic activity of 1-methyl-10-methoxydihydrolysergol 2-(3,5-dimethyl)pyrrolcarboxylate (XV, formula II) is, both in vitro and parenterally, quite similar to that of dihydroergotamine. By oral route the new compound is more active, and longer lasting than dihydroergotamine.


Subject(s)
Ergolines/chemical synthesis , Nicergoline/chemical synthesis , Sympatholytics/chemical synthesis , Administration, Oral , Animals , Delayed-Action Preparations , Dihydroergotamine/pharmacology , Guinea Pigs , Injections, Intravenous , Male , Nicergoline/administration & dosage , Nicergoline/analogs & derivatives , Receptors, Adrenergic, alpha/drug effects , Structure-Activity Relationship
2.
Farmaco Sci ; 30(10): 789-801, 1975 Oct.
Article in English | MEDLINE | ID: mdl-241664

ABSTRACT

The synthesis and the pharmacological activities of 24 analogues of the alpha-adrenergic blocking drug, nicergoline (I b), are reported. The majority of the new compounds were found to be less active than (I b): the structure-activity relationships are presented and discussed.


Subject(s)
Adrenergic alpha-Antagonists/chemical synthesis , Crystallization , Esters , Methylation , Nicergoline/analogs & derivatives , Nicergoline/chemical synthesis
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