Your browser doesn't support javascript.
loading
Synthesis, Anti-Cancer and Anti-Migratory Evaluation of 3,6-Dibromocarbazole and 5-Bromoindole Derivatives.
Butler-Fernández, Krystal M; Ramos, Zulma; Francis-Malavé, Adela M; Bloom, Joseph; Dharmawardhane, Suranganie; Hernández, Eliud.
Afiliación
  • Butler-Fernández KM; Department of Pharmaceutical Sciences, University of Puerto Rico, School of Pharmacy, San Juan 00936, Puerto Rico.
  • Ramos Z; Department of Pharmaceutical Sciences, University of Puerto Rico, School of Pharmacy, San Juan 00936, Puerto Rico.
  • Francis-Malavé AM; Department of Biology, College of Natural Sciences, University of Puerto Rico, San Juan 00931, Puerto Rico.
  • Bloom J; Department of Pharmaceutical Sciences, University of Puerto Rico, School of Pharmacy, San Juan 00936, Puerto Rico.
  • Dharmawardhane S; Department of Biochemistry, University of Puerto Rico, School of Medicine, San Juan 00936, Puerto Rico.
  • Hernández E; Department of Pharmaceutical Sciences, University of Puerto Rico, School of Pharmacy, San Juan 00936, Puerto Rico. eliud.hernandez@upr.edu.
Molecules ; 24(15)2019 Jul 24.
Article en En | MEDLINE | ID: mdl-31344865
ABSTRACT
In this study, a new series of N-alkyl-3,6-dibromocarbazole and N-alkyl-5-bromoindole derivatives have been synthesized and evaluated in vitro as anti-cancer and anti-migration agents. Cytotoxic and anti-migratory effects of these compounds were evaluated in MCF-7 and MDA-MB-231 breast cancer cell lines and an insight on the structure-activity relationship was developed. Preliminary investigations of their anti-cancer activity demonstrated that several compounds have moderate antiproliferative effects on cancer cell lines with GI50 values in the range of 4.7-32.2 µM. Moreover, carbazole derivatives 10, 14, 15, 23, and 24 inhibit migration activity of metastatic cell line MDA-MB-231 in the range of 18-20%. The effect of compounds 10, 14, and 15 in extension of invadopodia and filopodia was evaluated by fluorescence microscopy and results demonstrated a reduction in actin-based cell extensions by compounds 10 and 15.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carbazoles / Indoles / Antineoplásicos Límite: Humans Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Puerto Rico

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carbazoles / Indoles / Antineoplásicos Límite: Humans Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Puerto Rico
...