5-Methoxypsoralen
产品介绍
5-Methoxypsoralen是一种天然的抗炎剂与抗肿瘤剂,它能够抑制小鼠与人的细胞色素P450酶(CYP)亚型,同时作为一种补骨脂素,可被光活化,既能与脱氧核糖核酸(DNA)发生交叉连接,还能对蛋白质和脂质进行共价修饰,进而抑制细胞复制。
产品性质
产品特色
| 英文别名 (English Synonym) | 5-Methoxypsoralen |
| 中文名称 (Chinese Name) | 佛手柑内酯 |
| 靶点 (Target) | DNA/RNA Synthesis |
| 通路 (Pathway) | Natural Products |
| CAS号 (CAS NO.) | 484-20-8 |
| 分子式 (Formula) | C12H8O4 |
| 分子量 (Molecular Weight) | 216.19 |
| 纯度 (Purity) | ≥98% |
| 溶解性 (Solubility) | 溶于DMSO |
存储条件
-25~-15℃保存,有效期3年
COA
已发表文献
[1] Lee YM, Wu TH. Effects of 5-methoxypsoralen (5-MOP) on arylamine N-acetyltransferase activity in the stomach and colon of rats and human stomach and colon tumor cell lines. In Vivo. 2005 Nov-Dec;19(6):1061-9. PMID: 16277023.[2]Li XJ, Zhu Z, Han SL, Zhang ZL. Bergapten exerts inhibitory effects on diabetes-related osteoporosis via the regulation of the PI3K/AKT, JNK/MAPK and NF-κB signaling pathways in osteoprotegerin knockout mice. Int J Mol Med. 2016 Dec;38(6):1661-1672. doi: 10.3892/ijmm.2016.2794. Epub 2016 Nov 2. PMID: 27840967; PMCID: PMC5117769.
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