STRUCTURE OF β-CYCLODEXTRIN INCLUSION COMPLEX WITH NICOTINAMIDE
The crystal structure of the β-cyclodextrin-nicotinamide (1 : 1) complex hexahydrate was determined by the X-ray method. The β-cyclodextrin ring is round in shape with seven intramolecular hydrogen bonds between secondary hydroxyl groups. The nicotinamide molecule is included in the host β-cyclodext...
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Veröffentlicht in: | Chemical & pharmaceutical bulletin 1983/04/25, Vol.31(4), pp.1428-1430 |
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container_title | Chemical & pharmaceutical bulletin |
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creator | Harata, Kazuaki Kawano, Kenji Fukunaga, Kazuhiro Ohtani, Yoshiro |
description | The crystal structure of the β-cyclodextrin-nicotinamide (1 : 1) complex hexahydrate was determined by the X-ray method. The β-cyclodextrin ring is round in shape with seven intramolecular hydrogen bonds between secondary hydroxyl groups. The nicotinamide molecule is included in the host β-cyclodextrin cavity with the pyridine moiety being located at the center of the cavity. The amido group protrudes outside from the primary hydroxyl side of β-cyclodextrin and forms hydrogen bonds with adjacent β-cyclodextrin and water molecules. |
doi_str_mv | 10.1248/cpb.31.1428 |
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The β-cyclodextrin ring is round in shape with seven intramolecular hydrogen bonds between secondary hydroxyl groups. The nicotinamide molecule is included in the host β-cyclodextrin cavity with the pyridine moiety being located at the center of the cavity. The amido group protrudes outside from the primary hydroxyl side of β-cyclodextrin and forms hydrogen bonds with adjacent β-cyclodextrin and water molecules.</description><identifier>ISSN: 0009-2363</identifier><identifier>EISSN: 1347-5223</identifier><identifier>DOI: 10.1248/cpb.31.1428</identifier><language>eng</language><publisher>The Pharmaceutical Society of Japan</publisher><subject>crystal structure</subject><ispartof>Chemical and Pharmaceutical Bulletin, 1983/04/25, Vol.31(4), pp.1428-1430</ispartof><rights>The Pharmaceutical Society of Japan</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c424t-e9c8655c799d3befccd674561bddb25e143f857390685947bc96d5ee4c0c5e1f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,27901,27902</link.rule.ids></links><search><creatorcontrib>Harata, Kazuaki</creatorcontrib><creatorcontrib>Kawano, Kenji</creatorcontrib><creatorcontrib>Fukunaga, Kazuhiro</creatorcontrib><creatorcontrib>Ohtani, Yoshiro</creatorcontrib><title>STRUCTURE OF β-CYCLODEXTRIN INCLUSION COMPLEX WITH NICOTINAMIDE</title><title>Chemical & pharmaceutical bulletin</title><addtitle>Chem. Pharm. Bull.</addtitle><description>The crystal structure of the β-cyclodextrin-nicotinamide (1 : 1) complex hexahydrate was determined by the X-ray method. The β-cyclodextrin ring is round in shape with seven intramolecular hydrogen bonds between secondary hydroxyl groups. The nicotinamide molecule is included in the host β-cyclodextrin cavity with the pyridine moiety being located at the center of the cavity. The amido group protrudes outside from the primary hydroxyl side of β-cyclodextrin and forms hydrogen bonds with adjacent β-cyclodextrin and water molecules.</description><subject>crystal structure</subject><issn>0009-2363</issn><issn>1347-5223</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1983</creationdate><recordtype>article</recordtype><recordid>eNpFj81Og0AUhSdGE7G68gXYG3B-gdnZTGk7CQVDIdbVBIZB21RtGDa-lg_iMwnB6ObcxfnuST4AbhH0EabRvT7VPkE-ojg6Aw4iNPQYxuQcOBBC7mESkEtwZe0BQsxgSBzwsC3yUhRlHrvZ0v3-8sSzSLJFvCtymboyFUm5lVnqimzzmMQ790kWazeVIitkOt_IRXwNLtrqaM3N752BchkXYu0l2UqKeeJpimnvGa6jgDEdct6Q2rRaN0FIWYDqpqkxM4iSNmIh4TCIGKdhrXnQMGOohnpoWzIDd9Ou7j6s7UyrTt3-reo-FYJqlFeDvCJIjfIDvZjog-2rF_PHVl2_10czsoizaOTpFOPbf_1adcq8kx-B2GA1</recordid><startdate>19830101</startdate><enddate>19830101</enddate><creator>Harata, Kazuaki</creator><creator>Kawano, Kenji</creator><creator>Fukunaga, Kazuhiro</creator><creator>Ohtani, Yoshiro</creator><general>The Pharmaceutical Society of Japan</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19830101</creationdate><title>STRUCTURE OF β-CYCLODEXTRIN INCLUSION COMPLEX WITH NICOTINAMIDE</title><author>Harata, Kazuaki ; Kawano, Kenji ; Fukunaga, Kazuhiro ; Ohtani, Yoshiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c424t-e9c8655c799d3befccd674561bddb25e143f857390685947bc96d5ee4c0c5e1f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1983</creationdate><topic>crystal structure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harata, Kazuaki</creatorcontrib><creatorcontrib>Kawano, Kenji</creatorcontrib><creatorcontrib>Fukunaga, Kazuhiro</creatorcontrib><creatorcontrib>Ohtani, Yoshiro</creatorcontrib><collection>CrossRef</collection><jtitle>Chemical & pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harata, Kazuaki</au><au>Kawano, Kenji</au><au>Fukunaga, Kazuhiro</au><au>Ohtani, Yoshiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>STRUCTURE OF β-CYCLODEXTRIN INCLUSION COMPLEX WITH NICOTINAMIDE</atitle><jtitle>Chemical & pharmaceutical bulletin</jtitle><addtitle>Chem. Pharm. Bull.</addtitle><date>1983-01-01</date><risdate>1983</risdate><volume>31</volume><issue>4</issue><spage>1428</spage><epage>1430</epage><pages>1428-1430</pages><issn>0009-2363</issn><eissn>1347-5223</eissn><abstract>The crystal structure of the β-cyclodextrin-nicotinamide (1 : 1) complex hexahydrate was determined by the X-ray method. The β-cyclodextrin ring is round in shape with seven intramolecular hydrogen bonds between secondary hydroxyl groups. The nicotinamide molecule is included in the host β-cyclodextrin cavity with the pyridine moiety being located at the center of the cavity. The amido group protrudes outside from the primary hydroxyl side of β-cyclodextrin and forms hydrogen bonds with adjacent β-cyclodextrin and water molecules.</abstract><pub>The Pharmaceutical Society of Japan</pub><doi>10.1248/cpb.31.1428</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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source | J-STAGE Free; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Free Full-Text Journals in Chemistry |
subjects | crystal structure |
title | STRUCTURE OF β-CYCLODEXTRIN INCLUSION COMPLEX WITH NICOTINAMIDE |
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