Anticancer activities of Zanthoxylum bungeanum seed oil on malignant melanoma was written by Pang, Wenwen;Liu, Shan;He, Fangting;Li, Xinyang;Saira, Baloch;Zheng, Tianli;Chen, Jiayi;Dong, Ke;Pei, Xiao-fang. And the article was included in Journal of Ethnopharmacology in 2019.Application of 18836-52-7 The following contents are mentioned in the article:
Zanthoxylum bungeanum Maxim. (ZBM), a Chinese herb medicine and food additive, has been shown to have broad-spectrum beneficial effects. However, the anticancer activities of its seed have not been reported.for the first time investigated the anti-proliferation activity of seed oil of ZBM (ZBSO) on melanoma A375 cells as well as the underlying mechanisms. The chem. composition of ZBSO was analyzed by Ultra Performance Liquid Chromatog. A375 cells exposure at different concentrations of ZBSO to examine the selectivity vs. normal skin cells, invasion, apoptosis and cell cycle arrest. Furthermore, transcriptome anal. was employed to investigate potential anticancer mechanisms of ZBSO. Major compounds of ZBSO were identified and unsaturated fatty acid made up the major compound ZBSO-treated A375 cells showed more typical apoptotic morphol. features than normal cells. ZBSO can significantly inhibit invasion and proliferation of A375 cells by G1 phase arrest and induction of apoptosis. Transcriptome anal. showed that ZBSO may affect cell cycle and MAPK signaling pathway of A375 cells. ZBSO possessed anticancer activities that were selectively effective to A375 cells. This study support the hypothesis that ZBSO is a capable candidate for anti-melanoma agent, and provide new insights for future work on investigating the utilization of ZBSO in malignant melanoma treatment. This study involved multiple reactions and reactants, such as (2E,4E)-N-Isobutyldeca-2,4-dienamide (cas: 18836-52-7Application of 18836-52-7).
(2E,4E)-N-Isobutyldeca-2,4-dienamide (cas: 18836-52-7) belongs to amides. Amides can be viewed as a derivative of a carboxylic acid RC(=O)OH with the hydroxyl group –OH replaced by an amine group −NR′R″; or, equivalently, an acyl (alkanoyl) group RC(=O)− joined to an amine group. In simple aromatic amides, fragmentation occurs on both sides of the carbonyl group. If a hydrogen is available in N-substituted aromatic amides, it tends to migrate and form an aromatic amine and the loss of a ketene.Application of 18836-52-7
Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics