rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
3
|
pubmed:dateCreated |
1984-6-19
|
pubmed:abstractText |
The synthesis of a series of dialkylaminoalkylic esters of 1-chloro-3-carboxy-4-methylisoquinoline and of 1-chloro-3-carboxy-4-phenylisoquinoline is described. The pharmacological activity of some of these compounds was studied. The morpholinoethylester of 1-chloro-3-carboxy-4-methylisoquinoline (VIIa), dimethylaminoethylester (VIIb) and diethylaminoethylester (VIIc) showed a good antispasmodic activity. 4-Phenyl-derivatives (XVa), (XVb), (XVc) were more active than analogous 4-methyl derivatives; particularly the diethylaminoethylester of 1-chloro-3-carboxy-4-phenylisoquinoline (XVc) showed an antagonist effect against spasmogens similar to that of papaverine.
|
pubmed:language |
ita
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0430-0920
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
39
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
217-28
|
pubmed:dateRevised |
2009-6-5
|
pubmed:meshHeading |
pubmed-meshheading:6714415-Acetylcholine,
pubmed-meshheading:6714415-Analgesics,
pubmed-meshheading:6714415-Animals,
pubmed-meshheading:6714415-Anti-Inflammatory Agents,
pubmed-meshheading:6714415-Barium,
pubmed-meshheading:6714415-Central Nervous System,
pubmed-meshheading:6714415-Chemical Phenomena,
pubmed-meshheading:6714415-Chemistry,
pubmed-meshheading:6714415-Guinea Pigs,
pubmed-meshheading:6714415-Histamine Antagonists,
pubmed-meshheading:6714415-Isoquinolines,
pubmed-meshheading:6714415-Male,
pubmed-meshheading:6714415-Mice,
pubmed-meshheading:6714415-Motor Activity,
pubmed-meshheading:6714415-Parasympatholytics,
pubmed-meshheading:6714415-Rats,
pubmed-meshheading:6714415-Rats, Inbred Strains
|
pubmed:year |
1984
|
pubmed:articleTitle |
[Alkyl and aryl derivatives of isoquinoline. II. Synthesis and pharmacologic activity of dialkylaminoalkyl esters of 1-chloro-3-carboxy-4-methylisoquinoline and the corresponding 4-phenyl derivative].
|
pubmed:publicationType |
Journal Article,
In Vitro,
English Abstract,
Research Support, Non-U.S. Gov't
|