Cyclische Phenyl‐carbamate des Miotin‐Typs und ihre Wirkung auf die Acetylcholinesterase
Cyclic Phenyl Carbamates and Their Action on Acetylcholinesterase Several six‐, seven‐, and eight‐membered cyclic phenyl carbamates of the miotin type have been synthesised and their in vitro potency as inhibitors of acetylcholinesterase determined. The eight‐membered rings were found to be the most...
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Veröffentlicht in: | Helvetica chimica acta 1990-05, Vol.73 (3), p.739-753 |
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creator | Amstutz, René Enz, Albert Marzi, Martin Boelsterli, Jakob Walkinshaw, Malcolm |
description | Cyclic Phenyl Carbamates and Their Action on Acetylcholinesterase
Several six‐, seven‐, and eight‐membered cyclic phenyl carbamates of the miotin type have been synthesised and their in vitro potency as inhibitors of acetylcholinesterase determined. The eight‐membered rings were found to be the most potent and are comparable with physostigrnin or miotin. It was concluded that, for maximum potency, the orientation of the carbamate group relative to the aromatic plane has to be close to orthogonal. |
doi_str_mv | 10.1002/hlca.19900730323 |
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Several six‐, seven‐, and eight‐membered cyclic phenyl carbamates of the miotin type have been synthesised and their in vitro potency as inhibitors of acetylcholinesterase determined. The eight‐membered rings were found to be the most potent and are comparable with physostigrnin or miotin. It was concluded that, for maximum potency, the orientation of the carbamate group relative to the aromatic plane has to be close to orthogonal.</description><issn>0018-019X</issn><issn>1522-2675</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><recordid>eNqFkLFOwzAURS0EEqWwM_oHUp7tOk4GhioCilQEQxEMSJFjPxNDmlZ2KpSNT-Ab-RJSlYGN6UpP9zzpHkLOGUwYAL-oG6MnLM8BlADBxQEZMcl5wlMlD8kIgGUJsPz5mJzE-AYAQ1WNyEvRm8ZHUyN9qLHtm-_PL6NDpVe6Q2ox0ju_7nw7nJf9JtJta6mvA9InH9637SvVW0etRzoz2PWNqdeNbzF2GHTEU3LkdBPx7DfH5PH6alnMk8X9zW0xWySGQyYSaWXGTIqqQmatRC6qXKVcoBTDEC0rUEpMteFaTpXjzjhepVlmhRLWoWNiTGD_14R1jAFduQl-pUNfMih3dsqdnfKPnQG53CMfvsH-3345XxSzv_wPobxtqw</recordid><startdate>19900502</startdate><enddate>19900502</enddate><creator>Amstutz, René</creator><creator>Enz, Albert</creator><creator>Marzi, Martin</creator><creator>Boelsterli, Jakob</creator><creator>Walkinshaw, Malcolm</creator><general>WILEY‐VCH Verlag GmbH</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19900502</creationdate><title>Cyclische Phenyl‐carbamate des Miotin‐Typs und ihre Wirkung auf die Acetylcholinesterase</title><author>Amstutz, René ; Enz, Albert ; Marzi, Martin ; Boelsterli, Jakob ; Walkinshaw, Malcolm</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2083-5d581c6e7be1dd5e23b97623e53323a5b07734ac2a547f2fcf2b688d373dfef13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Amstutz, René</creatorcontrib><creatorcontrib>Enz, Albert</creatorcontrib><creatorcontrib>Marzi, Martin</creatorcontrib><creatorcontrib>Boelsterli, Jakob</creatorcontrib><creatorcontrib>Walkinshaw, Malcolm</creatorcontrib><collection>CrossRef</collection><jtitle>Helvetica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Amstutz, René</au><au>Enz, Albert</au><au>Marzi, Martin</au><au>Boelsterli, Jakob</au><au>Walkinshaw, Malcolm</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cyclische Phenyl‐carbamate des Miotin‐Typs und ihre Wirkung auf die Acetylcholinesterase</atitle><jtitle>Helvetica chimica acta</jtitle><date>1990-05-02</date><risdate>1990</risdate><volume>73</volume><issue>3</issue><spage>739</spage><epage>753</epage><pages>739-753</pages><issn>0018-019X</issn><eissn>1522-2675</eissn><abstract>Cyclic Phenyl Carbamates and Their Action on Acetylcholinesterase
Several six‐, seven‐, and eight‐membered cyclic phenyl carbamates of the miotin type have been synthesised and their in vitro potency as inhibitors of acetylcholinesterase determined. The eight‐membered rings were found to be the most potent and are comparable with physostigrnin or miotin. It was concluded that, for maximum potency, the orientation of the carbamate group relative to the aromatic plane has to be close to orthogonal.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag GmbH</pub><doi>10.1002/hlca.19900730323</doi><tpages>15</tpages></addata></record> |
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title | Cyclische Phenyl‐carbamate des Miotin‐Typs und ihre Wirkung auf die Acetylcholinesterase |
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