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Towards the synthesis of 27-Deoxylyngbyabellin A analogues as potential chemotherapeutics.
Towards the synthesis of 27-Deoxylyngbyabellin A analogues as potential chemotherapeutics.
Scarone, Laura; Sandin, Leonardo; Serra., Gloria
Abstract:
Natural products play an important role in drug development, particularly in anticancer, antibiotics and antiparasitics drugs. Marine cyanobacteria have been attracting increasing attention in drug discovery due to their structurally novel bioactive secondary metabolites. These natural products are predominantly modified peptides and depsipeptides, many of which happen to be cyclic. 27-Deoxylyngbyabellin A (1, figure 1), which was isolated from the cyanobacteria Lyngbya bouillonii, showed moderate cytotoxicity toward cancer cell lines HT29 and HeLa. As part of our search for compounds as candidates for anticancer or antiparasitic drugs employing molecular simplification, we are interested in the preparation of depsipeptides analogues of type 2. Herein, we presents the synthesis of fragment C4- C15 of depsipeptide of type 2 with X= O and R1= CH(CH3)2.
Natural products play an important role in drug development, particularly in anticancer, antibiotics and antiparasitics drugs. Marine cyanobacteria have been attracting increasing attention in drug discovery due to their structurally novel bioactive secondary metabolites. These natural products are predominantly modified peptides and depsipeptides, many of which happen to be cyclic. 27-Deoxylyngbyabellin A (1, figure 1), which was isolated from the cyanobacteria Lyngbya bouillonii, showed moderate cytotoxicity toward cancer cell lines HT29 and HeLa. As part of our search for compounds as candidates for anticancer or antiparasitic drugs employing molecular simplification, we are interested in the preparation of depsipeptides analogues of type 2. Herein, we presents the synthesis of fragment C4- C15 of depsipeptide of type 2 with X= O and R1= CH(CH3)2.
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DOI: 10.5151/chempro-15bmos-BMOS2013_2013813144948
Referências bibliográficas
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Como citar:
Scarone, Laura; Sandin, Leonardo; Serra., Gloria; "Towards the synthesis of 27-Deoxylyngbyabellin A analogues as potential chemotherapeutics.", p-151-151.
In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 2, Dezembro.2013.
São Paulo: Blucher,
2013.
ISSN 23184043,
DOI 10.5151/chempro-15bmos-BMOS2013_2013813144948
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TY - CONF T1 - Towards the synthesis of 27-Deoxylyngbyabellin A analogues as potential chemotherapeutics. JO - Blucher Chemistry Proceedings VL - 1 IS - 2 SP - 151 EP - 151 PY - 2013 T2 - Brazilian Meeting on Organic Synthesis 2013 AU - , , SN - 23184043 DO - http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_2013813144948 UR - www.proceedings.blucher.com.br/article-details/towards-the-synthesis-of-27-deoxylyngbyabellin-a-analogues-as-potential-chemotherapeutics-8371 KW - ER -
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@article{Scarone20144,
title="Towards the synthesis of 27-Deoxylyngbyabellin A analogues as potential chemotherapeutics.",
journal="Blucher Chemistry Proceedings",
volume="1",
number="2",
pages="151 - 151",
year="2013",
note="",
issn="23184043",
doi="http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_2013813144948",
url="www.proceedings.blucher.com.br/article-details/towards-the-synthesis-of-27-deoxylyngbyabellin-a-analogues-as-potential-chemotherapeutics-8371",
author="Laura Scarone", "Leonardo Sandin", "Gloria Serra.",
keywords="",
}
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Laura Scarone, Leonardo Sandin, Gloria Serra., Towards the synthesis of 27-Deoxylyngbyabellin A analogues as potential chemotherapeutics., Blucher Chemistry Proceedings, Volume 1, 2013, Pages 151-151, ISSN 23184043, http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_2013813144948 (www.proceedings.blucher.com.br/article-details/towards-the-synthesis-of-27-deoxylyngbyabellin-a-analogues-as-potential-chemotherapeutics-8371) Palavras-chave:: ;