@article{fdi:010055866,
  title = {{P}ipestelides {A}-{C} : cyclodepsipeptides from the {P}acific marine sponge {P}ipestela candelabra},
  author = {{S}orres, {J}. and {M}artin, {M}. {T}. and {P}etek, {S}ylvain and {L}evaique, {H}. and {C}resteil, {T}. and {R}amos, {S}. and {T}hoison, {O}. and {D}ebitus, {C}{\'e}cile and {A}l-{M}ourabit, {A}.},
  editor = {},
  language = {{ENG}},
  abstract = {{P}ipestelides {A}-{C} (2-4) are three new {NRPS}-{PKS} hybrid macrolides containing uncommon moieties, isolated from the {P}acific marine sponge {P}ipestela candelabra. {T}heir structures were elucidated on the basis of spectroscopic data. {T}hese cyclodepsipeptides appear to be biosynthetically related to jaspamide (aka jasplakinolide) (1) by chemical modification of the building blocks of the polyketide or peptide chains. {P}ipestelides {A}-{C} (2-4) contain a bromotyrosine [3-amino-3-(bromo-4-hydroxyphenyl)propanoic acid] unit, a polypropionate with a {Z} double bond, and a 2-hydroxyquinolinone, respectively. {R}evised chemical shift assignments are provided for the co-isolated known jasplakinolide {C}-a (5). {I}n addition, compounds 2 and 3 exhibited cytotoxic activities in the micromolar range.},
  keywords = {},
  booktitle = {},
  journal = {{J}ournal of {N}atural {P}roducts},
  volume = {75},
  numero = {4},
  pages = {759--763},
  ISSN = {0163-3864},
  year = {2012},
  DOI = {10.1021/np200714m},
  URL = {https://www.documentation.ird.fr/hor/fdi:010055866},
}