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Antineoplastic Agents. 604. The Path of Quinstatin Derivatives to Antibody Drug Conjugates.
Pettit, George R; Melody, Noeleen; Chapuis, Jean-Charles.
Afiliação
  • Pettit GR; Department of Chemistry and Biochemistry, Arizona State University , P.O. Box 871604, Tempe, Arizona 85287-1604, United States.
  • Melody N; Department of Chemistry and Biochemistry, Arizona State University , P.O. Box 871604, Tempe, Arizona 85287-1604, United States.
  • Chapuis JC; Department of Chemistry and Biochemistry, Arizona State University , P.O. Box 871604, Tempe, Arizona 85287-1604, United States.
J Nat Prod ; 80(9): 2447-2452, 2017 09 22.
Article em En | MEDLINE | ID: mdl-28895394
ABSTRACT
To further evaluate the exceptional cancer cell growth inhibition by the quinstatins, of which one of the series, quinstatin 8, approaches the exceptional cytotoxic activity of the parent dolastatin 10 (1), four of the quinstatins have been converted to desmethyl derivatives. Three of the four (4, 5, and 8 [7b-d]) were next bonded to the linker (8) employed in the synthesis of the very successful and structurally related anticancer drug Adcetris (3). Owing to these structural modifications, a next step could be taken by bonding to a monoclonal antibody, thereby producing an antibody drug conjugate (ADC) related to Adcetris structurally but with the possibility of a wider spectrum of activity and utility.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunoconjugados / Depsipeptídeos / Anticorpos Monoclonais / Antineoplásicos Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunoconjugados / Depsipeptídeos / Anticorpos Monoclonais / Antineoplásicos Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article