Your browser doesn't support javascript.
loading
Discovery of Mandelalide E and Determinants of Cytotoxicity for the Mandelalide Series.
Nazari, Mohamad; Serrill, Jeffrey D; Sikorska, Justyna; Ye, Tao; Ishmael, Jane E; McPhail, Kerry L.
Afiliación
  • Nazari M; Department of Pharmaceutical Sciences, Oregon State University , 203 Pharmacy Building, Corvallis, Oregon 97331-4003, United States.
  • Serrill JD; Department of Pharmaceutical Sciences, Oregon State University , 203 Pharmacy Building, Corvallis, Oregon 97331-4003, United States.
  • Sikorska J; Department of Pharmaceutical Sciences, Oregon State University , 203 Pharmacy Building, Corvallis, Oregon 97331-4003, United States.
  • Ye T; Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School Xili , Nanshan District, Shenzhen 518055, China.
  • Ishmael JE; Department of Pharmaceutical Sciences, Oregon State University , 203 Pharmacy Building, Corvallis, Oregon 97331-4003, United States.
  • McPhail KL; Department of Pharmaceutical Sciences, Oregon State University , 203 Pharmacy Building, Corvallis, Oregon 97331-4003, United States.
Org Lett ; 18(6): 1374-7, 2016 Mar 18.
Article en En | MEDLINE | ID: mdl-26914981
ABSTRACT
Recollection of the tunicate source of the mandelalides has provided new and known analogues that have facilitated expanded analyses of the disputed cancer cytotoxicity of mandelalide A following a number of recent reported total syntheses. Using newly characterized mandelalide E, reisolated natural mandelalides B and C, and synthetic mandelalide A, the cytotoxicity of the mandelalides is demonstrated to be strongly influenced by compound glycosylation and assay cell density. Glycosylated mandelalides reduced the viability of human cancer cells cultured at a high starting density with a rank order of potency A > B ≫ E, yet display dramatically reduced cytotoxic efficacy against low density cultures.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Macrólidos / Antineoplásicos Límite: Animals / Humans Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Macrólidos / Antineoplásicos Límite: Animals / Humans Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos