Macrolactone Nuiapolide, Isolated from a Hawaiian Marine Cyanobacterium, Exhibits Anti-Chemotactic Activity
A new bioactive macrolactone, nuiapolide (1) was identified from a marine cyanobacterium collected off the coast of Niihau, near Lehua Rock. The natural product exhibits anti-chemotactic activity at concentrations as low as 1.3 μM against Jurkat cells, cancerous T lymphocytes, and induces a G2/M pha...
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Online Access: | http://www.mdpi.com/1660-3397/13/10/6274 |
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doaj-a932d94d0e484730a580e970d4d6e7712020-11-24T22:29:55ZengMDPI AGMarine Drugs1660-33972015-10-0113106274629010.3390/md13106274md13106274Macrolactone Nuiapolide, Isolated from a Hawaiian Marine Cyanobacterium, Exhibits Anti-Chemotactic ActivityShogo Mori0Howard Williams1Davey Cagle2Kristopher Karanovich3F. David Horgen4Roger Smith III5Coran M. H. Watanabe6Department of Chemistry, Texas A&M University, College Station, TX 77843, USADepartment of Chemistry, Texas A&M University, College Station, TX 77843, USADepartment of Natural Sciences, Hawaii Pacific University, Kaneohe, HI 96744, USADepartment of Natural Sciences, Hawaii Pacific University, Kaneohe, HI 96744, USADepartment of Natural Sciences, Hawaii Pacific University, Kaneohe, HI 96744, USADepartment of Veterinary Pathology, Texas A&M University, College Station, TX 77843, USADepartment of Chemistry, Texas A&M University, College Station, TX 77843, USAA new bioactive macrolactone, nuiapolide (1) was identified from a marine cyanobacterium collected off the coast of Niihau, near Lehua Rock. The natural product exhibits anti-chemotactic activity at concentrations as low as 1.3 μM against Jurkat cells, cancerous T lymphocytes, and induces a G2/M phase cell cycle shift. Structural characterization of the natural product revealed the compound to be a 40-membered macrolactone with nine hydroxyl functional groups and a rare tert-butyl carbinol residue.http://www.mdpi.com/1660-3397/13/10/6274macrolactonepolyketidecyanobacteriachemotaxiscell cycle |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shogo Mori Howard Williams Davey Cagle Kristopher Karanovich F. David Horgen Roger Smith III Coran M. H. Watanabe |
spellingShingle |
Shogo Mori Howard Williams Davey Cagle Kristopher Karanovich F. David Horgen Roger Smith III Coran M. H. Watanabe Macrolactone Nuiapolide, Isolated from a Hawaiian Marine Cyanobacterium, Exhibits Anti-Chemotactic Activity Marine Drugs macrolactone polyketide cyanobacteria chemotaxis cell cycle |
author_facet |
Shogo Mori Howard Williams Davey Cagle Kristopher Karanovich F. David Horgen Roger Smith III Coran M. H. Watanabe |
author_sort |
Shogo Mori |
title |
Macrolactone Nuiapolide, Isolated from a Hawaiian Marine Cyanobacterium, Exhibits Anti-Chemotactic Activity |
title_short |
Macrolactone Nuiapolide, Isolated from a Hawaiian Marine Cyanobacterium, Exhibits Anti-Chemotactic Activity |
title_full |
Macrolactone Nuiapolide, Isolated from a Hawaiian Marine Cyanobacterium, Exhibits Anti-Chemotactic Activity |
title_fullStr |
Macrolactone Nuiapolide, Isolated from a Hawaiian Marine Cyanobacterium, Exhibits Anti-Chemotactic Activity |
title_full_unstemmed |
Macrolactone Nuiapolide, Isolated from a Hawaiian Marine Cyanobacterium, Exhibits Anti-Chemotactic Activity |
title_sort |
macrolactone nuiapolide, isolated from a hawaiian marine cyanobacterium, exhibits anti-chemotactic activity |
publisher |
MDPI AG |
series |
Marine Drugs |
issn |
1660-3397 |
publishDate |
2015-10-01 |
description |
A new bioactive macrolactone, nuiapolide (1) was identified from a marine cyanobacterium collected off the coast of Niihau, near Lehua Rock. The natural product exhibits anti-chemotactic activity at concentrations as low as 1.3 μM against Jurkat cells, cancerous T lymphocytes, and induces a G2/M phase cell cycle shift. Structural characterization of the natural product revealed the compound to be a 40-membered macrolactone with nine hydroxyl functional groups and a rare tert-butyl carbinol residue. |
topic |
macrolactone polyketide cyanobacteria chemotaxis cell cycle |
url |
http://www.mdpi.com/1660-3397/13/10/6274 |
work_keys_str_mv |
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