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N1-Benzyl Tryptamine Pan-SHIP1/2 Inhibitors: Synthesis and Preliminary Biological Evaluation as Anti-Tumor Agents.
Fernandes, Sandra; Meyer, Shea T; Shah, Jigisha P; Adhikari, Arijit A; Kerr, William G; Chisholm, John D.
Afiliação
  • Fernandes S; Department of Microbiology & Immunology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
  • Meyer ST; Department of Chemistry, Syracuse University, Syracuse, NY 13244, USA.
  • Shah JP; Department of Chemistry, Syracuse University, Syracuse, NY 13244, USA.
  • Adhikari AA; Department of Chemistry, Syracuse University, Syracuse, NY 13244, USA.
  • Kerr WG; Department of Microbiology & Immunology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
  • Chisholm JD; Department of Chemistry, Syracuse University, Syracuse, NY 13244, USA.
Molecules ; 27(23)2022 Dec 02.
Article em En | MEDLINE | ID: mdl-36500543
Inhibition of phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase (SHIP) with small molecule inhibitors leads to apoptosis in tumor cells. Inhibitors that target both SHIP1 and SHIP2 (pan-SHIP1/2 inhibitors) may have benefits in these areas since paralog compensation is not possible when both SHIP paralogs are being inhibited. A series of tryptamine-based pan-SHIP1/2 inhibitors have been synthesized and evaluated for their ability to inhibit the SHIP paralogs. The most active compounds were also evaluated for their effects on cancer cell lines.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias / Antineoplásicos Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias / Antineoplásicos Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article