| CAS NO: | 500-65-2 |
| 包装 | 价格(元) |
| 1mg | 电议 |
| 5mg | 电议 |
| 10mg | 电议 |
| 25mg | 电议 |
| Physical Appearance | A crystalline solid |
| Storage | Store at -20°C |
| M.Wt | 258.3 |
| Cas No. | 500-65-2 |
| Formula | C15H14O4 |
| Solubility | ≤30mg/ml in ethanol;30mg/ml in DMSO;30mg/ml in dimethyl formamide |
| Chemical Name | 5-[(1E)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]-1,3-benzenediol |
| Canonical SMILES | COc1ccc(/C=C\c2cc(O)cc(O)c2)cc1O |
| 运输条件 | 蓝冰运输或根据您的需求运输。 |
| 一般建议 | 为了使其更好的溶解，请用37℃加热试管并在超声波水浴中震动片刻。不同厂家不同批次产品溶解度各有差异，仅做参考。若实验所需浓度过大至产品溶解极限，请添加助溶剂助溶或自行调整浓度。溶液形式一般不宜长期储存，请尽快用完。 |
Rhapontigenin is an apoptosis-inducing agent, and also a potent and selective cytochrome P450 1A1 inhibitor with IC50 value of 0.4 μM [1][2].
Human cytochrome P450 (P450) 1A1 is an aryl hydrocarbon hydroxylase which involved in the metabolic activation of procarcinogens of the polycyclic aromatic hydrocarbons. P450 1A1 is mainly expressed in human lung, placenta, and lymphocytes. Selective inhibitors of P450 1A1 may be good chemopreventive agent candidates for cancer [2].
Rhapontigenin is an apoptosis-inducing agent and a cytochrome P450 1A1 inhibitor. Rhapontigenin inhibited recombinant human cytochrome P450 (P450) 1A1 with IC50 value of 0.4 μM. Rhapontigenin showed 400-fold and 23-fold selectivity for P450 1A1 over P450 1A2 and P450 1B1, respectively. Rhapontigenin showed competitive inhibition of P450 1A1 with Ki value of 0.21 μM [1]. Rhapontigenin is a natural analog of resveratrol, a potential cancer chemopreventive agent. In the HL60 cell line, Rhapontigenin inhibited cell proliferation with IC50 value of 48 μM [2]. In Hep G2 hepatoma cells, Rhapontigenin exhibited concentration-dependent anti-cancer activity with IC50 value of 115 μg/mL [3].
References:
[1]. Chun YJ, Ryu SY, Jeong TC, et al. Mechanism-based inhibition of human cytochrome P450 1A1 by rhapontigenin. Drug Metab Dispos. 2001 Apr;29(4 Pt 1):389-93.
[2]. Roberti M1, Pizzirani D, Simoni D, et al. Synthesis and biological evaluation of resveratrol and analogues as apoptosis-inducing agents. J Med Chem. 2003 Jul 31;46(16):3546-54.
[3]. Roupe KA1, Helms GL, Halls SC, et al. Preparative enzymatic synthesis and HPLC analysis of rhapontigenin: applications to metabolism, pharmacokinetics and anti-cancer studies. J Pharm Pharm Sci. 2005 Aug 22;8(3):374-86.
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