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PNEUMOCANDINS FROM Zalerion arboricola: III. STRUCTURE ELUCIDATION
Pneumocandin B0 (6) and six related lipopeptides are antifungal and anti-Pneumocystis carinii agents from mutants of Zalerion arboricola, whose structures were determined mainly on the basis of spectroscopic analysis. They belong, along with pneumocandin A0 (L-671, 329) previously isolated from thes...
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Published in: | Journal of antibiotics 1992/12/25, Vol.45(12), pp.1875-1885 |
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container_end_page | 1885 |
container_issue | 12 |
container_start_page | 1875 |
container_title | Journal of antibiotics |
container_volume | 45 |
creator | HENSENS, OTTO D. LIESCH, JERROLD M. ZINK, DEBORAH L. SMITH, JACK L. WICHMANN, CAROL F. SCHWARTZ, ROBERT E. |
description | Pneumocandin B0 (6) and six related lipopeptides are antifungal and anti-Pneumocystis carinii agents from mutants of Zalerion arboricola, whose structures were determined mainly on the basis of spectroscopic analysis. They belong, along with pneumocandin A0 (L-671, 329) previously isolated from these laboratories, 1) to the echinocandin class of antifungal agents. The product from base-catalyzed ring opening involving the hemiaminal position of the dihydroxyornithine residue of B0, has been clearly defined as 6b. Modifications were limited to the 3-hydroxy-4-methylproline, 3, 4-dihydroxyhomotyrosine and 4, 5-dihydroxyornithine residues of pneumocandin A0. |
doi_str_mv | 10.7164/antibiotics.45.1875 |
format | article |
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STRUCTURE ELUCIDATION</title><title>Journal of antibiotics</title><addtitle>J. Antibiot.</addtitle><description>Pneumocandin B0 (6) and six related lipopeptides are antifungal and anti-Pneumocystis carinii agents from mutants of Zalerion arboricola, whose structures were determined mainly on the basis of spectroscopic analysis. They belong, along with pneumocandin A0 (L-671, 329) previously isolated from these laboratories, 1) to the echinocandin class of antifungal agents. The product from base-catalyzed ring opening involving the hemiaminal position of the dihydroxyornithine residue of B0, has been clearly defined as 6b. Modifications were limited to the 3-hydroxy-4-methylproline, 3, 4-dihydroxyhomotyrosine and 4, 5-dihydroxyornithine residues of pneumocandin A0.</description><subject>Anti-Bacterial Agents</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Antifungal agents</subject><subject>Antifungal Agents - chemistry</subject><subject>Antifungal Agents - pharmacology</subject><subject>Antiviral Agents - chemistry</subject><subject>Biological and medical sciences</subject><subject>Candida albicans - drug effects</subject><subject>Crystallography</subject><subject>Echinocandins</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Medical sciences</subject><subject>Mitosporic Fungi - chemistry</subject><subject>Peptides</subject><subject>Peptides, Cyclic - chemistry</subject><subject>Peptides, Cyclic - pharmacology</subject><subject>Pharmacology. 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Antiinfectious agents. Antiparasitic agents</topic><topic>Antifungal agents</topic><topic>Antifungal Agents - chemistry</topic><topic>Antifungal Agents - pharmacology</topic><topic>Antiviral Agents - chemistry</topic><topic>Biological and medical sciences</topic><topic>Candida albicans - drug effects</topic><topic>Crystallography</topic><topic>Echinocandins</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Medical sciences</topic><topic>Mitosporic Fungi - chemistry</topic><topic>Peptides</topic><topic>Peptides, Cyclic - chemistry</topic><topic>Peptides, Cyclic - pharmacology</topic><topic>Pharmacology. 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STRUCTURE ELUCIDATION</atitle><jtitle>Journal of antibiotics</jtitle><addtitle>J. Antibiot.</addtitle><date>1992</date><risdate>1992</risdate><volume>45</volume><issue>12</issue><spage>1875</spage><epage>1885</epage><pages>1875-1885</pages><issn>0021-8820</issn><eissn>1881-1469</eissn><coden>JANTAJ</coden><abstract>Pneumocandin B0 (6) and six related lipopeptides are antifungal and anti-Pneumocystis carinii agents from mutants of Zalerion arboricola, whose structures were determined mainly on the basis of spectroscopic analysis. They belong, along with pneumocandin A0 (L-671, 329) previously isolated from these laboratories, 1) to the echinocandin class of antifungal agents. The product from base-catalyzed ring opening involving the hemiaminal position of the dihydroxyornithine residue of B0, has been clearly defined as 6b. 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language | eng |
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source | J-STAGE (Japan Science & Technology Information Aggregator, Electronic) - Open Access English articles |
subjects | Anti-Bacterial Agents Antibiotics. Antiinfectious agents. Antiparasitic agents Antifungal agents Antifungal Agents - chemistry Antifungal Agents - pharmacology Antiviral Agents - chemistry Biological and medical sciences Candida albicans - drug effects Crystallography Echinocandins Magnetic Resonance Spectroscopy Medical sciences Mitosporic Fungi - chemistry Peptides Peptides, Cyclic - chemistry Peptides, Cyclic - pharmacology Pharmacology. Drug treatments Pneumocystis - drug effects Stereoisomerism Structure-Activity Relationship |
title | PNEUMOCANDINS FROM Zalerion arboricola: III. STRUCTURE ELUCIDATION |
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