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Synthesis and evaluation of a ring-constrained Hsp90 C-terminal inhibitor that exhibits neuroprotective activity.
Zhang, Zheng; You, Zhenyuan; Dobrowsky, Rick T; Blagg, Brian S J.
Afiliação
  • Zhang Z; Department of Chemistry and Biochemistry, The University of Notre Dame, 251 Nieuwland Science Hall, Notre Dame, IN 46556, United States.
  • You Z; Department of Pharmacology and Toxicology Department, The University of Kansas, Lawrence, KS 66045, United States.
  • Dobrowsky RT; Department of Pharmacology and Toxicology Department, The University of Kansas, Lawrence, KS 66045, United States.
  • Blagg BSJ; Department of Chemistry and Biochemistry, The University of Notre Dame, 251 Nieuwland Science Hall, Notre Dame, IN 46556, United States. Electronic address: bblagg@nd.edu.
Bioorg Med Chem Lett ; 28(16): 2701-2704, 2018 09 01.
Article em En | MEDLINE | ID: mdl-29759728
KU-596 is a second-generation C-terminal heat shock protein 90 KDa (Hsp90) modulator based on the natural product, novobiocin. KU-596 has been shown to induce Hsp70 levels and manifest neuroprotective activity through induction of the heat shock response. A ring-constrained analog of KU-596 was designed and synthesized to probe its binding orientation and ability to induce Hsp70 levels. Compound 2 was found to exhibit comparable or increased activity compared to KU-596, which is under clinical investigation for the treatment of neuropathy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenantridinas / Fármacos Neuroprotetores / Proteínas de Choque Térmico HSP90 / Glicosídeos / Lactamas Limite: Animals Idioma: En Revista: Bioorg Med Chem Lett Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenantridinas / Fármacos Neuroprotetores / Proteínas de Choque Térmico HSP90 / Glicosídeos / Lactamas Limite: Animals Idioma: En Revista: Bioorg Med Chem Lett Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos