The structure of the bafilomycins, a new group of macrolide antibiotics
The structure of bafilomycins A 1, B 2, B 1, B 2, C 1 and C 2, produced by Streptomyces griseus ssp. sulphurus has been elucidated mainly by spectroscopic studies. The bafilomycins are macrolide antibiotics with a 16-membered lactone ring.
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Veröffentlicht in: | Tetrahedron letters 1983, Vol.24 (47), p.5193-5196 |
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container_issue | 47 |
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container_title | Tetrahedron letters |
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creator | Werner, Gerhard Hagenmaier, Hanspaul Albert, Klaus Kohlshorn, Heinz |
description | The structure of bafilomycins
A
1, B
2, B
1, B
2, C
1
and
C
2,
produced by
Streptomyces griseus ssp. sulphurus
has been elucidated mainly by spectroscopic studies. The bafilomycins are macrolide antibiotics with a 16-membered lactone ring. |
doi_str_mv | 10.1016/S0040-4039(00)88394-X |
format | Article |
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A
1, B
2, B
1, B
2, C
1
and
C
2,
produced by
Streptomyces griseus ssp. sulphurus
has been elucidated mainly by spectroscopic studies. The bafilomycins are macrolide antibiotics with a 16-membered lactone ring.</description><identifier>ISSN: 0040-4039</identifier><identifier>EISSN: 1873-3581</identifier><identifier>DOI: 10.1016/S0040-4039(00)88394-X</identifier><identifier>CODEN: TELEAY</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Antibiotics (antibacterial agents, antifungal agents) ; Antibiotics, microbial producers, chemotherapic agents, antiseptics, disinfecting agents ; Applied microbiology ; Biological and medical sciences ; Fundamental and applied biological sciences. Psychology ; Microbiology ; Streptomyces griseus</subject><ispartof>Tetrahedron letters, 1983, Vol.24 (47), p.5193-5196</ispartof><rights>1982</rights><rights>1984 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-c381847451e399c03af1b44fd709121f0b38be134643cbfb11116b1c65185f753</citedby><cites>FETCH-LOGICAL-c433t-c381847451e399c03af1b44fd709121f0b38be134643cbfb11116b1c65185f753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S004040390088394X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,4010,27900,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9559226$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Werner, Gerhard</creatorcontrib><creatorcontrib>Hagenmaier, Hanspaul</creatorcontrib><creatorcontrib>Albert, Klaus</creatorcontrib><creatorcontrib>Kohlshorn, Heinz</creatorcontrib><title>The structure of the bafilomycins, a new group of macrolide antibiotics</title><title>Tetrahedron letters</title><description>The structure of bafilomycins
A
1, B
2, B
1, B
2, C
1
and
C
2,
produced by
Streptomyces griseus ssp. sulphurus
has been elucidated mainly by spectroscopic studies. The bafilomycins are macrolide antibiotics with a 16-membered lactone ring.</description><subject>Antibiotics (antibacterial agents, antifungal agents)</subject><subject>Antibiotics, microbial producers, chemotherapic agents, antiseptics, disinfecting agents</subject><subject>Applied microbiology</subject><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Microbiology</subject><subject>Streptomyces griseus</subject><issn>0040-4039</issn><issn>1873-3581</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1983</creationdate><recordtype>article</recordtype><recordid>eNqFkF1LwzAUhoMoOKc_QeiFiILVc5akTa9Ehk5h4IUTdhfSNNFI186kVfbvzT7Yre_NgcPzno-XkHOEWwTM7t4AGKQMaHEFcC0ELVg6PyADFDlNKRd4SAZ75JichPAFUZmAAZnMPk0SOt_rrvcmaW3SxUaprKvbxUq7JtwkKmnMb_Lh2365BhZK-7Z2lUlU07nStZ3T4ZQcWVUHc7arQ_L-9DgbP6fT18nL-GGaakZpl2oqULCccTS0KDRQZbFkzFY5FDhCCyUVpUHKMkZ1aUuMykrUGUfBbc7pkFxu5y59-92b0MmFC9rUtWpM2weJtICM5SKCfAvGY0PwxsqldwvlVxJBrmOTm9jkOhMJIDexyXn0XewWqKBVbb1qtAt7c8F5MRplEbvfYiY---OMl0E702hTOW90J6vW_bPoD3EigEc</recordid><startdate>1983</startdate><enddate>1983</enddate><creator>Werner, Gerhard</creator><creator>Hagenmaier, Hanspaul</creator><creator>Albert, Klaus</creator><creator>Kohlshorn, Heinz</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>1983</creationdate><title>The structure of the bafilomycins, a new group of macrolide antibiotics</title><author>Werner, Gerhard ; Hagenmaier, Hanspaul ; Albert, Klaus ; Kohlshorn, Heinz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-c381847451e399c03af1b44fd709121f0b38be134643cbfb11116b1c65185f753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1983</creationdate><topic>Antibiotics (antibacterial agents, antifungal agents)</topic><topic>Antibiotics, microbial producers, chemotherapic agents, antiseptics, disinfecting agents</topic><topic>Applied microbiology</topic><topic>Biological and medical sciences</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Microbiology</topic><topic>Streptomyces griseus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Werner, Gerhard</creatorcontrib><creatorcontrib>Hagenmaier, Hanspaul</creatorcontrib><creatorcontrib>Albert, Klaus</creatorcontrib><creatorcontrib>Kohlshorn, Heinz</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Tetrahedron letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Werner, Gerhard</au><au>Hagenmaier, Hanspaul</au><au>Albert, Klaus</au><au>Kohlshorn, Heinz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The structure of the bafilomycins, a new group of macrolide antibiotics</atitle><jtitle>Tetrahedron letters</jtitle><date>1983</date><risdate>1983</risdate><volume>24</volume><issue>47</issue><spage>5193</spage><epage>5196</epage><pages>5193-5196</pages><issn>0040-4039</issn><eissn>1873-3581</eissn><coden>TELEAY</coden><abstract>The structure of bafilomycins
A
1, B
2, B
1, B
2, C
1
and
C
2,
produced by
Streptomyces griseus ssp. sulphurus
has been elucidated mainly by spectroscopic studies. The bafilomycins are macrolide antibiotics with a 16-membered lactone ring.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/S0040-4039(00)88394-X</doi><tpages>4</tpages></addata></record> |
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issn | 0040-4039 1873-3581 |
language | eng |
recordid | cdi_proquest_miscellaneous_13906478 |
source | Elsevier ScienceDirect Journals |
subjects | Antibiotics (antibacterial agents, antifungal agents) Antibiotics, microbial producers, chemotherapic agents, antiseptics, disinfecting agents Applied microbiology Biological and medical sciences Fundamental and applied biological sciences. Psychology Microbiology Streptomyces griseus |
title | The structure of the bafilomycins, a new group of macrolide antibiotics |
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