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From meiogynin A to the synthesis of dual inhibitors of Bcl-xL and Mcl-1 anti-apoptotic proteins.
Desrat, S; Remeur, C; Gény, C; Rivière, G; Colas, C; Dumontet, V; Birlirakis, N; Iorga, B I; Roussi, F.
Affiliation
  • Desrat S; Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles (ICSN), CNRS UPR 2301, 1 av de la Terrasse, 91 198 Gif-sur-Yvette Cedex, France. fanny.roussi@cnrs.fr.
Chem Commun (Camb) ; 50(62): 8593-6, 2014 Aug 11.
Article in En | MEDLINE | ID: mdl-24956071
The synthesis of one of the most potent dual inhibitors of the anti-apoptotic proteins Bcl-xL and Mcl-1 is reported. This analogue of a natural sesquiterpenoid dimer meiogynin A was elaborated by a convergent asymmetric synthesis with 36% yield in ten steps.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sesquiterpenes / Bcl-X Protein / Cycloaddition Reaction / Myeloid Cell Leukemia Sequence 1 Protein Type of study: Prognostic_studies Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2014 Document type: Article Affiliation country: Francia Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sesquiterpenes / Bcl-X Protein / Cycloaddition Reaction / Myeloid Cell Leukemia Sequence 1 Protein Type of study: Prognostic_studies Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2014 Document type: Article Affiliation country: Francia Country of publication: Reino Unido