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Mollamides B and C, Cyclic Hexapeptides from the Indonesian Tunicate Didemnum molle

[Image: see text] Two new cyclic hexapeptides, mollamides B (1) and C (2), were isolated from the Indonesian tunicate Didemnum molle along with the known peptide keenamide A (3). The structures were established using 1D and 2D NMR experiments. The relative configuration of mollamide B at the thiazol...

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Autores principales: Donia, Marwa S., Wang, Bin, Dunbar, Daniel C., Desai, Prashant V., Patny, Akshay, Avery, Mitchell, Hamann, Mark T.
Formato: Texto
Lenguaje:English
Publicado: American Chemical Society and American Society of Pharmacognosy 2008
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2651694/
https://www.ncbi.nlm.nih.gov/pubmed/18543965
http://dx.doi.org/10.1021/np700718p
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author Donia, Marwa S.
Wang, Bin
Dunbar, Daniel C.
Desai, Prashant V.
Patny, Akshay
Avery, Mitchell
Hamann, Mark T.
author_facet Donia, Marwa S.
Wang, Bin
Dunbar, Daniel C.
Desai, Prashant V.
Patny, Akshay
Avery, Mitchell
Hamann, Mark T.
author_sort Donia, Marwa S.
collection PubMed
description [Image: see text] Two new cyclic hexapeptides, mollamides B (1) and C (2), were isolated from the Indonesian tunicate Didemnum molle along with the known peptide keenamide A (3). The structures were established using 1D and 2D NMR experiments. The relative configuration of mollamide B at the thiazoline moiety was determined using molecular modeling coupled with NMR-derived restraints. Their absolute configuration was determined using Marfeyʼs method. The new peptides have been evaluated for their antimicrobial, antimalarial, anticancer, anti-HIV-1, anti-Mtb, and anti-inflammatory activities. Keenamide A and mollamide B show cytotoxicity against several cancer cell lines.
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spelling pubmed-26516942009-03-20 Mollamides B and C, Cyclic Hexapeptides from the Indonesian Tunicate Didemnum molle Donia, Marwa S. Wang, Bin Dunbar, Daniel C. Desai, Prashant V. Patny, Akshay Avery, Mitchell Hamann, Mark T. J Nat Prod [Image: see text] Two new cyclic hexapeptides, mollamides B (1) and C (2), were isolated from the Indonesian tunicate Didemnum molle along with the known peptide keenamide A (3). The structures were established using 1D and 2D NMR experiments. The relative configuration of mollamide B at the thiazoline moiety was determined using molecular modeling coupled with NMR-derived restraints. Their absolute configuration was determined using Marfeyʼs method. The new peptides have been evaluated for their antimicrobial, antimalarial, anticancer, anti-HIV-1, anti-Mtb, and anti-inflammatory activities. Keenamide A and mollamide B show cytotoxicity against several cancer cell lines. American Chemical Society and American Society of Pharmacognosy 2008-06-11 2008-06-27 /pmc/articles/PMC2651694/ /pubmed/18543965 http://dx.doi.org/10.1021/np700718p Text en Copyright © 2008 American Chemical Society and American Society of Pharmacognosy http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. 40.75
spellingShingle Donia, Marwa S.
Wang, Bin
Dunbar, Daniel C.
Desai, Prashant V.
Patny, Akshay
Avery, Mitchell
Hamann, Mark T.
Mollamides B and C, Cyclic Hexapeptides from the Indonesian Tunicate Didemnum molle
title Mollamides B and C, Cyclic Hexapeptides from the Indonesian Tunicate Didemnum molle
title_full Mollamides B and C, Cyclic Hexapeptides from the Indonesian Tunicate Didemnum molle
title_fullStr Mollamides B and C, Cyclic Hexapeptides from the Indonesian Tunicate Didemnum molle
title_full_unstemmed Mollamides B and C, Cyclic Hexapeptides from the Indonesian Tunicate Didemnum molle
title_short Mollamides B and C, Cyclic Hexapeptides from the Indonesian Tunicate Didemnum molle
title_sort mollamides b and c, cyclic hexapeptides from the indonesian tunicate didemnum molle
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2651694/
https://www.ncbi.nlm.nih.gov/pubmed/18543965
http://dx.doi.org/10.1021/np700718p
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