Cargando…

Synthesis, Identification and Anti-Cancer Activity of 1-(4-Methylpent-2-enyl)-2-(4-phenylbut-2-enyl)disulfane

In this study, we synthesized 1-(4-methylpent-2-enyl)-2-(4-phenylbut-2- enyl)disulfane using sodium sulfide, 1-bromine-4-methyl-2-amylene and 1-(4-bromine-2- butylene)benzene as raw materials. The yield rate of target product was 84%. The structure of the target product was confirmed by GC-MS, (1)H-...

Descripción completa

Detalles Bibliográficos
Autores principales: Ji, Chunxiao, Ren, Fenglian, Xu, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257707/
https://www.ncbi.nlm.nih.gov/pubmed/20714320
http://dx.doi.org/10.3390/molecules15085671
_version_ 1783374375087505408
author Ji, Chunxiao
Ren, Fenglian
Xu, Ming
author_facet Ji, Chunxiao
Ren, Fenglian
Xu, Ming
author_sort Ji, Chunxiao
collection PubMed
description In this study, we synthesized 1-(4-methylpent-2-enyl)-2-(4-phenylbut-2- enyl)disulfane using sodium sulfide, 1-bromine-4-methyl-2-amylene and 1-(4-bromine-2- butylene)benzene as raw materials. The yield rate of target product was 84%. The structure of the target product was confirmed by GC-MS, (1)H-NMR and elemental analysis. The results of anti-cancer activity experiments showed that 1-(4-methylpent-2-enyl)-2-(4- phenylbut-2-enyl)disulfane could significantly inhibit the proliferation, induce the apoptosis of CNE2 cells in a dose dependent manner, and could significantly enhance the activity of XIAP.
format Online
Article
Text
id pubmed-6257707
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-62577072018-12-06 Synthesis, Identification and Anti-Cancer Activity of 1-(4-Methylpent-2-enyl)-2-(4-phenylbut-2-enyl)disulfane Ji, Chunxiao Ren, Fenglian Xu, Ming Molecules Communication In this study, we synthesized 1-(4-methylpent-2-enyl)-2-(4-phenylbut-2- enyl)disulfane using sodium sulfide, 1-bromine-4-methyl-2-amylene and 1-(4-bromine-2- butylene)benzene as raw materials. The yield rate of target product was 84%. The structure of the target product was confirmed by GC-MS, (1)H-NMR and elemental analysis. The results of anti-cancer activity experiments showed that 1-(4-methylpent-2-enyl)-2-(4- phenylbut-2-enyl)disulfane could significantly inhibit the proliferation, induce the apoptosis of CNE2 cells in a dose dependent manner, and could significantly enhance the activity of XIAP. MDPI 2010-08-16 /pmc/articles/PMC6257707/ /pubmed/20714320 http://dx.doi.org/10.3390/molecules15085671 Text en © 2010 by the authors; http://creativecommons.org/licenses/by/3.0/ licensee MDPI, Basel, Switzerland. This article is an Open Access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Communication
Ji, Chunxiao
Ren, Fenglian
Xu, Ming
Synthesis, Identification and Anti-Cancer Activity of 1-(4-Methylpent-2-enyl)-2-(4-phenylbut-2-enyl)disulfane
title Synthesis, Identification and Anti-Cancer Activity of 1-(4-Methylpent-2-enyl)-2-(4-phenylbut-2-enyl)disulfane
title_full Synthesis, Identification and Anti-Cancer Activity of 1-(4-Methylpent-2-enyl)-2-(4-phenylbut-2-enyl)disulfane
title_fullStr Synthesis, Identification and Anti-Cancer Activity of 1-(4-Methylpent-2-enyl)-2-(4-phenylbut-2-enyl)disulfane
title_full_unstemmed Synthesis, Identification and Anti-Cancer Activity of 1-(4-Methylpent-2-enyl)-2-(4-phenylbut-2-enyl)disulfane
title_short Synthesis, Identification and Anti-Cancer Activity of 1-(4-Methylpent-2-enyl)-2-(4-phenylbut-2-enyl)disulfane
title_sort synthesis, identification and anti-cancer activity of 1-(4-methylpent-2-enyl)-2-(4-phenylbut-2-enyl)disulfane
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257707/
https://www.ncbi.nlm.nih.gov/pubmed/20714320
http://dx.doi.org/10.3390/molecules15085671
work_keys_str_mv AT jichunxiao synthesisidentificationandanticanceractivityof14methylpent2enyl24phenylbut2enyldisulfane
AT renfenglian synthesisidentificationandanticanceractivityof14methylpent2enyl24phenylbut2enyldisulfane
AT xuming synthesisidentificationandanticanceractivityof14methylpent2enyl24phenylbut2enyldisulfane