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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1986-7-14
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pubmed:abstractText |
Unnatural (+)-physostigmine (2) inhibited acetylcholinesterase (AChE) from electric eel considerably less than natural (-)-physostigmine (1), but 2 may because of its possible lower toxicity still be an interesting anticholinesterase agent. (-)-Eseroline (3), a major metabolite of (-)-physostigmine (1) and a potent narcotic analgetic, and its unnatural (+)-antipode (4), were both poor inhibitors of the enzyme. (-)-Dihydrosecophysostigmine (5), a ring-open analog of (-)-physostigmine was less, but (-)-N-methylphysostigmine (6) much more potent than the natural alkaloid. The availability of compounds related to (-)- and (+)-physostigmine by improved chemical synthesis suggests that further structural variation may well lead to other biologically interesting AChE inhibitors.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acetylcholinesterase,
http://linkedlifedata.com/resource/pubmed/chemical/Cholinesterase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Indoles,
http://linkedlifedata.com/resource/pubmed/chemical/Physostigmine,
http://linkedlifedata.com/resource/pubmed/chemical/eseroline
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0014-5793
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
9
|
pubmed:volume |
201
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
|
pubmed:pagination |
190-2
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:3709808-Acetylcholinesterase,
pubmed-meshheading:3709808-Animals,
pubmed-meshheading:3709808-Cholinesterase Inhibitors,
pubmed-meshheading:3709808-Eels,
pubmed-meshheading:3709808-Indoles,
pubmed-meshheading:3709808-Physostigmine,
pubmed-meshheading:3709808-Structure-Activity Relationship
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pubmed:year |
1986
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pubmed:articleTitle |
Inhibition of acetylcholinesterase from electric eel by (-)-and (+)-physostigmine and related compounds.
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pubmed:publicationType |
Journal Article,
Comparative Study
|