Progress in the Chemistry of Organic Natural Products/Progrès Dans La Chimie Des Substances Organiques Naturelles:
Gespeichert in:
1. Verfasser: | |
---|---|
Format: | Elektronisch E-Book |
Sprache: | German |
Veröffentlicht: |
Vienna
Springer Vienna
1963
|
Schriftenreihe: | Fortschritte Der Chemie Organischer Naturstoffe
21 |
Schlagworte: | |
Online-Zugang: | Volltext |
Beschreibung: | During the early 1950's there appeared reports, from time to time of the presence among the products elaborated by actinomycetes of antifungal antibiotics which exhibited very similar and very characteristic multipeaked ultraviolet absorption spectra. In 1954, with a good number of examples on record, these spectra were analyzed and identified as those of straight-chain conjugated polyenes, comprising tetraenes, pentaenes, hexaenes and heptaenes (85, I30). These antibiotics have since been commonly referred to as the polyene antifungal antibiotics to distinguish them from a host of other miscellaneous antibiotics which also have antifungal properties. Within the next few years, reports of discoveries of new members of this class multiplied rapidly, and almost sixty are now known. Unquestionably, a number of these will eventually be found to be identical with others, as has already happened in several instances: for example, the tetraene "tennecetin" proved to be a rediscovery of pimaricin (34), and in the methyl pentaenes "moldcidin E" has been identified with pentamycin (83), and "lagosin" appears to be indistinguishable from fungichromin (22). Those that have been purified have turned out to be of fairly high molecular weight (ca. 700-1300) and all appear to be substances of rather similar molecular structure. So far only three, pimaricin, fungi chromin (lagosin) and filipin, have been structurally elucidated |
Beschreibung: | 1 Online-Ressource (VIII, 364 S. 2 Abb) |
ISBN: | 9783709171493 9783709171509 |
ISSN: | 0071-7886 |
DOI: | 10.1007/978-3-7091-7149-3 |
Internformat
MARC
LEADER | 00000nmm a2200000zcb4500 | ||
---|---|---|---|
001 | BV042452919 | ||
003 | DE-604 | ||
005 | 00000000000000.0 | ||
007 | cr|uuu---uuuuu | ||
008 | 150324s1963 |||| o||u| ||||||ger d | ||
020 | |a 9783709171493 |c Online |9 978-3-7091-7149-3 | ||
020 | |a 9783709171509 |c Print |9 978-3-7091-7150-9 | ||
024 | 7 | |a 10.1007/978-3-7091-7149-3 |2 doi | |
035 | |a (OCoLC)863794937 | ||
035 | |a (DE-599)BVBBV042452919 | ||
040 | |a DE-604 |b ger |e aacr | ||
041 | 0 | |a ger | |
049 | |a DE-91 |a DE-634 |a DE-92 |a DE-706 | ||
082 | 0 | |a 547 |2 23 | |
084 | |a NAT 000 |2 stub | ||
100 | 1 | |a Bangert, R. |e Verfasser |4 aut | |
245 | 1 | 0 | |a Progress in the Chemistry of Organic Natural Products/Progrès Dans La Chimie Des Substances Organiques Naturelles |c von R. Bangert, J. Bonner, H. Brockmann, L. Crombie, L. Jaenicke, C. Kutzbach, A. D. Mebane, H. Muxfeldt, W. Oroshnik ; herausgegeben von L. Zechmeister |
264 | 1 | |a Vienna |b Springer Vienna |c 1963 | |
300 | |a 1 Online-Ressource (VIII, 364 S. 2 Abb) | ||
336 | |b txt |2 rdacontent | ||
337 | |b c |2 rdamedia | ||
338 | |b cr |2 rdacarrier | ||
490 | 0 | |a Fortschritte Der Chemie Organischer Naturstoffe |v 21 |x 0071-7886 | |
500 | |a During the early 1950's there appeared reports, from time to time of the presence among the products elaborated by actinomycetes of antifungal antibiotics which exhibited very similar and very characteristic multipeaked ultraviolet absorption spectra. In 1954, with a good number of examples on record, these spectra were analyzed and identified as those of straight-chain conjugated polyenes, comprising tetraenes, pentaenes, hexaenes and heptaenes (85, I30). These antibiotics have since been commonly referred to as the polyene antifungal antibiotics to distinguish them from a host of other miscellaneous antibiotics which also have antifungal properties. Within the next few years, reports of discoveries of new members of this class multiplied rapidly, and almost sixty are now known. Unquestionably, a number of these will eventually be found to be identical with others, as has already happened in several instances: for example, the tetraene "tennecetin" proved to be a rediscovery of pimaricin (34), and in the methyl pentaenes "moldcidin E" has been identified with pentamycin (83), and "lagosin" appears to be indistinguishable from fungichromin (22). Those that have been purified have turned out to be of fairly high molecular weight (ca. 700-1300) and all appear to be substances of rather similar molecular structure. So far only three, pimaricin, fungi chromin (lagosin) and filipin, have been structurally elucidated | ||
650 | 4 | |a Chemistry | |
650 | 4 | |a Toxicology | |
650 | 4 | |a Chemistry, Organic | |
650 | 4 | |a Pharmacy | |
650 | 4 | |a Biochemistry | |
650 | 4 | |a Botany | |
650 | 4 | |a Organic Chemistry | |
650 | 4 | |a Biochemistry, general | |
650 | 4 | |a Pharmacology/Toxicology | |
650 | 4 | |a Plant Sciences | |
650 | 4 | |a Chemie | |
700 | 1 | |a Bonner, J. |e Sonstige |4 oth | |
700 | 1 | |a Brockmann, H. |e Sonstige |4 oth | |
700 | 1 | |a Crombie, L. |e Sonstige |4 oth | |
700 | 1 | |a Jaenicke, L. |e Sonstige |4 oth | |
700 | 1 | |a Kutzbach, C. |e Sonstige |4 oth | |
700 | 1 | |a Mebane, A. D. |e Sonstige |4 oth | |
700 | 1 | |a Muxfeldt, H. |e Sonstige |4 oth | |
700 | 1 | |a Oroshnik, W. |e Sonstige |4 oth | |
700 | 1 | |a Zechmeister, L. |e Sonstige |4 oth | |
856 | 4 | 0 | |u https://doi.org/10.1007/978-3-7091-7149-3 |x Verlag |3 Volltext |
912 | |a ZDB-2-SNA |a ZDB-2-BAD | ||
940 | 1 | |q ZDB-2-SNA_Archive | |
999 | |a oai:aleph.bib-bvb.de:BVB01-027888165 |
Datensatz im Suchindex
_version_ | 1804153157416124416 |
---|---|
any_adam_object | |
author | Bangert, R. |
author_facet | Bangert, R. |
author_role | aut |
author_sort | Bangert, R. |
author_variant | r b rb |
building | Verbundindex |
bvnumber | BV042452919 |
classification_tum | NAT 000 |
collection | ZDB-2-SNA ZDB-2-BAD |
ctrlnum | (OCoLC)863794937 (DE-599)BVBBV042452919 |
dewey-full | 547 |
dewey-hundreds | 500 - Natural sciences and mathematics |
dewey-ones | 547 - Organic chemistry |
dewey-raw | 547 |
dewey-search | 547 |
dewey-sort | 3547 |
dewey-tens | 540 - Chemistry and allied sciences |
discipline | Chemie / Pharmazie Allgemeine Naturwissenschaft |
doi_str_mv | 10.1007/978-3-7091-7149-3 |
format | Electronic eBook |
fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>03548nmm a2200601zcb4500</leader><controlfield tag="001">BV042452919</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">00000000000000.0</controlfield><controlfield tag="007">cr|uuu---uuuuu</controlfield><controlfield tag="008">150324s1963 |||| o||u| ||||||ger d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9783709171493</subfield><subfield code="c">Online</subfield><subfield code="9">978-3-7091-7149-3</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9783709171509</subfield><subfield code="c">Print</subfield><subfield code="9">978-3-7091-7150-9</subfield></datafield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/978-3-7091-7149-3</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)863794937</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV042452919</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">aacr</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">ger</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-91</subfield><subfield code="a">DE-634</subfield><subfield code="a">DE-92</subfield><subfield code="a">DE-706</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">547</subfield><subfield code="2">23</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">NAT 000</subfield><subfield code="2">stub</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Bangert, R.</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Progress in the Chemistry of Organic Natural Products/Progrès Dans La Chimie Des Substances Organiques Naturelles</subfield><subfield code="c">von R. Bangert, J. Bonner, H. Brockmann, L. Crombie, L. Jaenicke, C. Kutzbach, A. D. Mebane, H. Muxfeldt, W. Oroshnik ; herausgegeben von L. Zechmeister</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Vienna</subfield><subfield code="b">Springer Vienna</subfield><subfield code="c">1963</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 Online-Ressource (VIII, 364 S. 2 Abb)</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="490" ind1="0" ind2=" "><subfield code="a">Fortschritte Der Chemie Organischer Naturstoffe</subfield><subfield code="v">21</subfield><subfield code="x">0071-7886</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">During the early 1950's there appeared reports, from time to time of the presence among the products elaborated by actinomycetes of antifungal antibiotics which exhibited very similar and very characteristic multipeaked ultraviolet absorption spectra. In 1954, with a good number of examples on record, these spectra were analyzed and identified as those of straight-chain conjugated polyenes, comprising tetraenes, pentaenes, hexaenes and heptaenes (85, I30). These antibiotics have since been commonly referred to as the polyene antifungal antibiotics to distinguish them from a host of other miscellaneous antibiotics which also have antifungal properties. Within the next few years, reports of discoveries of new members of this class multiplied rapidly, and almost sixty are now known. Unquestionably, a number of these will eventually be found to be identical with others, as has already happened in several instances: for example, the tetraene "tennecetin" proved to be a rediscovery of pimaricin (34), and in the methyl pentaenes "moldcidin E" has been identified with pentamycin (83), and "lagosin" appears to be indistinguishable from fungichromin (22). Those that have been purified have turned out to be of fairly high molecular weight (ca. 700-1300) and all appear to be substances of rather similar molecular structure. So far only three, pimaricin, fungi chromin (lagosin) and filipin, have been structurally elucidated</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chemistry</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Toxicology</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chemistry, Organic</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Pharmacy</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Biochemistry</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Botany</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Organic Chemistry</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Biochemistry, general</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Pharmacology/Toxicology</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Plant Sciences</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chemie</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bonner, J.</subfield><subfield code="e">Sonstige</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Brockmann, H.</subfield><subfield code="e">Sonstige</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Crombie, L.</subfield><subfield code="e">Sonstige</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Jaenicke, L.</subfield><subfield code="e">Sonstige</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kutzbach, C.</subfield><subfield code="e">Sonstige</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Mebane, A. D.</subfield><subfield code="e">Sonstige</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Muxfeldt, H.</subfield><subfield code="e">Sonstige</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Oroshnik, W.</subfield><subfield code="e">Sonstige</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zechmeister, L.</subfield><subfield code="e">Sonstige</subfield><subfield code="4">oth</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1007/978-3-7091-7149-3</subfield><subfield code="x">Verlag</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-2-SNA</subfield><subfield code="a">ZDB-2-BAD</subfield></datafield><datafield tag="940" ind1="1" ind2=" "><subfield code="q">ZDB-2-SNA_Archive</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-027888165</subfield></datafield></record></collection> |
id | DE-604.BV042452919 |
illustrated | Not Illustrated |
indexdate | 2024-07-10T01:22:09Z |
institution | BVB |
isbn | 9783709171493 9783709171509 |
issn | 0071-7886 |
language | German |
oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-027888165 |
oclc_num | 863794937 |
open_access_boolean | |
owner | DE-91 DE-BY-TUM DE-634 DE-92 DE-706 |
owner_facet | DE-91 DE-BY-TUM DE-634 DE-92 DE-706 |
physical | 1 Online-Ressource (VIII, 364 S. 2 Abb) |
psigel | ZDB-2-SNA ZDB-2-BAD ZDB-2-SNA_Archive |
publishDate | 1963 |
publishDateSearch | 1963 |
publishDateSort | 1963 |
publisher | Springer Vienna |
record_format | marc |
series2 | Fortschritte Der Chemie Organischer Naturstoffe |
spelling | Bangert, R. Verfasser aut Progress in the Chemistry of Organic Natural Products/Progrès Dans La Chimie Des Substances Organiques Naturelles von R. Bangert, J. Bonner, H. Brockmann, L. Crombie, L. Jaenicke, C. Kutzbach, A. D. Mebane, H. Muxfeldt, W. Oroshnik ; herausgegeben von L. Zechmeister Vienna Springer Vienna 1963 1 Online-Ressource (VIII, 364 S. 2 Abb) txt rdacontent c rdamedia cr rdacarrier Fortschritte Der Chemie Organischer Naturstoffe 21 0071-7886 During the early 1950's there appeared reports, from time to time of the presence among the products elaborated by actinomycetes of antifungal antibiotics which exhibited very similar and very characteristic multipeaked ultraviolet absorption spectra. In 1954, with a good number of examples on record, these spectra were analyzed and identified as those of straight-chain conjugated polyenes, comprising tetraenes, pentaenes, hexaenes and heptaenes (85, I30). These antibiotics have since been commonly referred to as the polyene antifungal antibiotics to distinguish them from a host of other miscellaneous antibiotics which also have antifungal properties. Within the next few years, reports of discoveries of new members of this class multiplied rapidly, and almost sixty are now known. Unquestionably, a number of these will eventually be found to be identical with others, as has already happened in several instances: for example, the tetraene "tennecetin" proved to be a rediscovery of pimaricin (34), and in the methyl pentaenes "moldcidin E" has been identified with pentamycin (83), and "lagosin" appears to be indistinguishable from fungichromin (22). Those that have been purified have turned out to be of fairly high molecular weight (ca. 700-1300) and all appear to be substances of rather similar molecular structure. So far only three, pimaricin, fungi chromin (lagosin) and filipin, have been structurally elucidated Chemistry Toxicology Chemistry, Organic Pharmacy Biochemistry Botany Organic Chemistry Biochemistry, general Pharmacology/Toxicology Plant Sciences Chemie Bonner, J. Sonstige oth Brockmann, H. Sonstige oth Crombie, L. Sonstige oth Jaenicke, L. Sonstige oth Kutzbach, C. Sonstige oth Mebane, A. D. Sonstige oth Muxfeldt, H. Sonstige oth Oroshnik, W. Sonstige oth Zechmeister, L. Sonstige oth https://doi.org/10.1007/978-3-7091-7149-3 Verlag Volltext |
spellingShingle | Bangert, R. Progress in the Chemistry of Organic Natural Products/Progrès Dans La Chimie Des Substances Organiques Naturelles Chemistry Toxicology Chemistry, Organic Pharmacy Biochemistry Botany Organic Chemistry Biochemistry, general Pharmacology/Toxicology Plant Sciences Chemie |
title | Progress in the Chemistry of Organic Natural Products/Progrès Dans La Chimie Des Substances Organiques Naturelles |
title_auth | Progress in the Chemistry of Organic Natural Products/Progrès Dans La Chimie Des Substances Organiques Naturelles |
title_exact_search | Progress in the Chemistry of Organic Natural Products/Progrès Dans La Chimie Des Substances Organiques Naturelles |
title_full | Progress in the Chemistry of Organic Natural Products/Progrès Dans La Chimie Des Substances Organiques Naturelles von R. Bangert, J. Bonner, H. Brockmann, L. Crombie, L. Jaenicke, C. Kutzbach, A. D. Mebane, H. Muxfeldt, W. Oroshnik ; herausgegeben von L. Zechmeister |
title_fullStr | Progress in the Chemistry of Organic Natural Products/Progrès Dans La Chimie Des Substances Organiques Naturelles von R. Bangert, J. Bonner, H. Brockmann, L. Crombie, L. Jaenicke, C. Kutzbach, A. D. Mebane, H. Muxfeldt, W. Oroshnik ; herausgegeben von L. Zechmeister |
title_full_unstemmed | Progress in the Chemistry of Organic Natural Products/Progrès Dans La Chimie Des Substances Organiques Naturelles von R. Bangert, J. Bonner, H. Brockmann, L. Crombie, L. Jaenicke, C. Kutzbach, A. D. Mebane, H. Muxfeldt, W. Oroshnik ; herausgegeben von L. Zechmeister |
title_short | Progress in the Chemistry of Organic Natural Products/Progrès Dans La Chimie Des Substances Organiques Naturelles |
title_sort | progress in the chemistry of organic natural products progres dans la chimie des substances organiques naturelles |
topic | Chemistry Toxicology Chemistry, Organic Pharmacy Biochemistry Botany Organic Chemistry Biochemistry, general Pharmacology/Toxicology Plant Sciences Chemie |
topic_facet | Chemistry Toxicology Chemistry, Organic Pharmacy Biochemistry Botany Organic Chemistry Biochemistry, general Pharmacology/Toxicology Plant Sciences Chemie |
url | https://doi.org/10.1007/978-3-7091-7149-3 |
work_keys_str_mv | AT bangertr progressinthechemistryoforganicnaturalproductsprogresdanslachimiedessubstancesorganiquesnaturelles AT bonnerj progressinthechemistryoforganicnaturalproductsprogresdanslachimiedessubstancesorganiquesnaturelles AT brockmannh progressinthechemistryoforganicnaturalproductsprogresdanslachimiedessubstancesorganiquesnaturelles AT crombiel progressinthechemistryoforganicnaturalproductsprogresdanslachimiedessubstancesorganiquesnaturelles AT jaenickel progressinthechemistryoforganicnaturalproductsprogresdanslachimiedessubstancesorganiquesnaturelles AT kutzbachc progressinthechemistryoforganicnaturalproductsprogresdanslachimiedessubstancesorganiquesnaturelles AT mebanead progressinthechemistryoforganicnaturalproductsprogresdanslachimiedessubstancesorganiquesnaturelles AT muxfeldth progressinthechemistryoforganicnaturalproductsprogresdanslachimiedessubstancesorganiquesnaturelles AT oroshnikw progressinthechemistryoforganicnaturalproductsprogresdanslachimiedessubstancesorganiquesnaturelles AT zechmeisterl progressinthechemistryoforganicnaturalproductsprogresdanslachimiedessubstancesorganiquesnaturelles |