The Structural Characterization of Amavadin
Fly agaric accumulate vanadium in the form of amavadin, whose structure has been elucidated (see picture for the crystal structure). Amavadin contains one VIV center coordinated to two (S,S)‐hidpa3− ligands (H3hidpa=2,2′‐(hydroxyimino)dipropionic acid) through one η2‐NO− group and two unidentate car...
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Veröffentlicht in: | Angewandte Chemie International Edition 1999-03, Vol.38 (6), p.795-797 |
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creator | Berry, Robert E. Armstrong, Elaine M. Beddoes, Roy L. Collison, David Ertok, S. Nigar Helliwell, Madeleine Garner, C. David |
description | Fly agaric accumulate vanadium in the form of amavadin, whose structure has been elucidated (see picture for the crystal structure). Amavadin contains one VIV center coordinated to two (S,S)‐hidpa3− ligands (H3hidpa=2,2′‐(hydroxyimino)dipropionic acid) through one η2‐NO− group and two unidentate carboxylato groups from each ligand. The arrangement of the two η2‐NO− groups leads to a chiral vanadium center, which has been characterized in both the Λ and Δ forms. The carboxylato groups of the amavadin anions bind cations, for example, Ca2+ ions, and/or become involved in hydrogen bonding. |
doi_str_mv | 10.1002/(SICI)1521-3773(19990315)38:6<795::AID-ANIE795>3.0.CO;2-7 |
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Nigar ; Helliwell, Madeleine ; Garner, C. David</creator><creatorcontrib>Berry, Robert E. ; Armstrong, Elaine M. ; Beddoes, Roy L. ; Collison, David ; Ertok, S. Nigar ; Helliwell, Madeleine ; Garner, C. David</creatorcontrib><description>Fly agaric accumulate vanadium in the form of amavadin, whose structure has been elucidated (see picture for the crystal structure). Amavadin contains one VIV center coordinated to two (S,S)‐hidpa3− ligands (H3hidpa=2,2′‐(hydroxyimino)dipropionic acid) through one η2‐NO− group and two unidentate carboxylato groups from each ligand. The arrangement of the two η2‐NO− groups leads to a chiral vanadium center, which has been characterized in both the Λ and Δ forms. The carboxylato groups of the amavadin anions bind cations, for example, Ca2+ ions, and/or become involved in hydrogen bonding.</description><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/(SICI)1521-3773(19990315)38:6<795::AID-ANIE795>3.0.CO;2-7</identifier><identifier>PMID: 29711812</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag GmbH</publisher><subject>Amavadin ; Bioinorganic chemistry ; Chirality ; Natural products ; Structure elucidation ; Vanadium</subject><ispartof>Angewandte Chemie International Edition, 1999-03, Vol.38 (6), p.795-797</ispartof><rights>1999 WILEY‐VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany</rights><rights>1999 WILEY-VCH Verlag GmbH, Weinheim, Fed. 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Nigar</creatorcontrib><creatorcontrib>Helliwell, Madeleine</creatorcontrib><creatorcontrib>Garner, C. David</creatorcontrib><title>The Structural Characterization of Amavadin</title><title>Angewandte Chemie International Edition</title><addtitle>Angewandte Chemie International Edition</addtitle><description>Fly agaric accumulate vanadium in the form of amavadin, whose structure has been elucidated (see picture for the crystal structure). Amavadin contains one VIV center coordinated to two (S,S)‐hidpa3− ligands (H3hidpa=2,2′‐(hydroxyimino)dipropionic acid) through one η2‐NO− group and two unidentate carboxylato groups from each ligand. The arrangement of the two η2‐NO− groups leads to a chiral vanadium center, which has been characterized in both the Λ and Δ forms. The carboxylato groups of the amavadin anions bind cations, for example, Ca2+ ions, and/or become involved in hydrogen bonding.</description><subject>Amavadin</subject><subject>Bioinorganic chemistry</subject><subject>Chirality</subject><subject>Natural products</subject><subject>Structure elucidation</subject><subject>Vanadium</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkGtr2zAUhkXZ6G39CyMfU4bTI53akrIxMG6XGUqy0ZYxGBxkW6HenLiT7F7266uQy5cN9kkXXj3v0cNYymHEAcTZ8DrP8lMeCx6hlDjkWmtAHp-iGicfpI7H4zS_iNJpfhkOH3EEo2z2XkRyjx3uXr0K-3PESKqYH7Aj738GtFKQ7LMDoSXniotD9u7mzg6uO9eXXe9MM8jujDNlZ139x3R1uxy080G6MA-mqpdv2Ou5abw92azH7PbT5U32ObqaTfIsvYrKOOFxxEFLU4BMAEsTQyEl1wKtnlegua04CiG4sImSRSWFCR87N4XBSptSa7QKj9lwzb137e_e-o4WtS9t05ilbXtPAhBRKg0Qot_X0dK13js7p3tXL4x7Jg60ckm0ckkrK7SyQluXhIoSCvqIgkvauCQkoGxGgmRgv92M0RcLW-3IW3kh8GMdeKwb-_xX83-L_927vQr4aI2vfWefdnjjflEiUcb0bTqhKVxkMPn6hQS-AD-2nTw</recordid><startdate>19990315</startdate><enddate>19990315</enddate><creator>Berry, Robert E.</creator><creator>Armstrong, Elaine M.</creator><creator>Beddoes, Roy L.</creator><creator>Collison, David</creator><creator>Ertok, S. 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David</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5615-1097ab07603ca50b771923e9fd091ed1322212e687bd72a0314aba3d9ac993e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Amavadin</topic><topic>Bioinorganic chemistry</topic><topic>Chirality</topic><topic>Natural products</topic><topic>Structure elucidation</topic><topic>Vanadium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Berry, Robert E.</creatorcontrib><creatorcontrib>Armstrong, Elaine M.</creatorcontrib><creatorcontrib>Beddoes, Roy L.</creatorcontrib><creatorcontrib>Collison, David</creatorcontrib><creatorcontrib>Ertok, S. Nigar</creatorcontrib><creatorcontrib>Helliwell, Madeleine</creatorcontrib><creatorcontrib>Garner, C. David</creatorcontrib><collection>Istex</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Berry, Robert E.</au><au>Armstrong, Elaine M.</au><au>Beddoes, Roy L.</au><au>Collison, David</au><au>Ertok, S. Nigar</au><au>Helliwell, Madeleine</au><au>Garner, C. David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Structural Characterization of Amavadin</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angewandte Chemie International Edition</addtitle><date>1999-03-15</date><risdate>1999</risdate><volume>38</volume><issue>6</issue><spage>795</spage><epage>797</epage><pages>795-797</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><abstract>Fly agaric accumulate vanadium in the form of amavadin, whose structure has been elucidated (see picture for the crystal structure). Amavadin contains one VIV center coordinated to two (S,S)‐hidpa3− ligands (H3hidpa=2,2′‐(hydroxyimino)dipropionic acid) through one η2‐NO− group and two unidentate carboxylato groups from each ligand. The arrangement of the two η2‐NO− groups leads to a chiral vanadium center, which has been characterized in both the Λ and Δ forms. The carboxylato groups of the amavadin anions bind cations, for example, Ca2+ ions, and/or become involved in hydrogen bonding.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag GmbH</pub><pmid>29711812</pmid><doi>10.1002/(SICI)1521-3773(19990315)38:6<795::AID-ANIE795>3.0.CO;2-7</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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source | Wiley Online Library Journals Frontfile Complete |
subjects | Amavadin Bioinorganic chemistry Chirality Natural products Structure elucidation Vanadium |
title | The Structural Characterization of Amavadin |
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