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Cytotoxic Dimeric Epipolythiodiketopiperazines from the Ascomycetous Fungus Preussia typharum

[Image: see text] Two new dimeric epipolythiodiketopiperazines, preussiadins A (1) and B (2), together with two known diastereomers, leptosins C (6) and A (7), were obtained from the mycelia of a Preussia typharum isolate. The structures of the new compounds were established by spectroscopic methods...

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Autores principales: Du, Lin, Robles, Andrew J., King, Jarrod B., Mooberry, Susan L., Cichewicz, Robert H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society and American Society of Pharmacognosy 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4073660/
https://www.ncbi.nlm.nih.gov/pubmed/24893224
http://dx.doi.org/10.1021/np5002253
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author Du, Lin
Robles, Andrew J.
King, Jarrod B.
Mooberry, Susan L.
Cichewicz, Robert H.
author_facet Du, Lin
Robles, Andrew J.
King, Jarrod B.
Mooberry, Susan L.
Cichewicz, Robert H.
author_sort Du, Lin
collection PubMed
description [Image: see text] Two new dimeric epipolythiodiketopiperazines, preussiadins A (1) and B (2), together with two known diastereomers, leptosins C (6) and A (7), were obtained from the mycelia of a Preussia typharum isolate. The structures of the new compounds were established by spectroscopic methods, and the absolute configurations of 1 and 2 were assigned by chemical transformations and comparisons of quantum chemical ECD and VCD calculations to experimental data. Compound 1 exhibited potent cytotoxic activity in the NCI-60 cell line panel with an average LC(50) value of 251 nM. Further studies demonstrated that 1 circumvents P-glycoprotein-mediated drug resistance, yet had no significant antitumor activity in a xenograft UACC-62 melanoma model.
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spelling pubmed-40736602015-06-03 Cytotoxic Dimeric Epipolythiodiketopiperazines from the Ascomycetous Fungus Preussia typharum Du, Lin Robles, Andrew J. King, Jarrod B. Mooberry, Susan L. Cichewicz, Robert H. J Nat Prod [Image: see text] Two new dimeric epipolythiodiketopiperazines, preussiadins A (1) and B (2), together with two known diastereomers, leptosins C (6) and A (7), were obtained from the mycelia of a Preussia typharum isolate. The structures of the new compounds were established by spectroscopic methods, and the absolute configurations of 1 and 2 were assigned by chemical transformations and comparisons of quantum chemical ECD and VCD calculations to experimental data. Compound 1 exhibited potent cytotoxic activity in the NCI-60 cell line panel with an average LC(50) value of 251 nM. Further studies demonstrated that 1 circumvents P-glycoprotein-mediated drug resistance, yet had no significant antitumor activity in a xenograft UACC-62 melanoma model. American Chemical Society and American Society of Pharmacognosy 2014-06-03 2014-06-27 /pmc/articles/PMC4073660/ /pubmed/24893224 http://dx.doi.org/10.1021/np5002253 Text en Copyright © 2014 American Chemical Society and American Society of Pharmacognosy Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Du, Lin
Robles, Andrew J.
King, Jarrod B.
Mooberry, Susan L.
Cichewicz, Robert H.
Cytotoxic Dimeric Epipolythiodiketopiperazines from the Ascomycetous Fungus Preussia typharum
title Cytotoxic Dimeric Epipolythiodiketopiperazines from the Ascomycetous Fungus Preussia typharum
title_full Cytotoxic Dimeric Epipolythiodiketopiperazines from the Ascomycetous Fungus Preussia typharum
title_fullStr Cytotoxic Dimeric Epipolythiodiketopiperazines from the Ascomycetous Fungus Preussia typharum
title_full_unstemmed Cytotoxic Dimeric Epipolythiodiketopiperazines from the Ascomycetous Fungus Preussia typharum
title_short Cytotoxic Dimeric Epipolythiodiketopiperazines from the Ascomycetous Fungus Preussia typharum
title_sort cytotoxic dimeric epipolythiodiketopiperazines from the ascomycetous fungus preussia typharum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4073660/
https://www.ncbi.nlm.nih.gov/pubmed/24893224
http://dx.doi.org/10.1021/np5002253
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