产品分类

补骨脂乙素
品牌:北京金优科技有限公司
货号 规格 包装/纯度 价格 货期 操作
JY-2025IT675mg 5mg HPLC≥98%
¥300.00
生物活性: 靶点:AKT
通路:PI3K/Akt/mTOR
背景说明:据报道,能诱导成神经细胞瘤凋亡。
生物活性:Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1].
IC50:7.92μM(OVCAR-8 cell)[1]
In Vitro:Isobavachalcone(6.0-48.0 μM; 72 hours; OVCAR-8,PC3,A549,MCF-7,L-02 and HUVEC cells)treatment inhibits the proliferation of human cancer cells. Isobavachalcone inhibits PC3,A549,MCF-7,L-02 and HUVEC cells growth with IC50 values of 15.06 μM,32.2 μM,28.29 μM,31.61 μM and 31.3 μM,respectively.Isobavachalcone(0-18 μM; 6 hours; OVCAR-8 and PC3 cells)treatment results in a concentration-and time-dependent down-regulation of the Ser-473 phosphorylation of Akt and GSK3b phosphorylation.Isobavachalcone(0-18 μM; 72 hours; OVCAR-8 and PC3 cells)treatment causes apoptosis via caspase- and ROS-involved mitochondrial pathway[1].
In Vivo:Isobavachalcone(20 mg/kg; intraperitoneal injection; for 0.5-24 hours; female Kunming mice)treatment results in an increase in blood glucose levels,reaching a maximum within 1 hour and maintaining until 4 hours post-dosing[1].
数据来源文献:[1]. Jing H, et al. Abrogation of Akt signaling by Isobavachalcone contributes to its anti-proliferative effects towards human cancer cells. Cancer Lett. 2010 Aug 28;294(2):167-77.
其它标识: MDL:MFCD00902090
SMILES:O=C(/C=C/C1=CC=C(C=C1)O)C2=CC=C(C(C/C=C(C)\C)=C2O)O
InChIKey:DUWPGRAKHMEPCM-IZZDOVSWSA-N
InChI:InChI=1S/C20H20O4/c1-13(2)3-9-16-19(23)12-10-17(20(16)24)18(22)11-6-14-4-7-15(21)8-5-14/h3-8,10-12,21,23-24H,9H2,1-2H3/b11-6+
PubChem CID:5281255
基本信息: CAS:20784-50-3
中文名称:补骨脂乙素
英文名称:Isobavachalcone
别名:4-Hydroxyisocordoim;异补骨脂查尔酮
分子式:C20H20O4
分子量:324.38
规格:10mg ; 10mM*1mL in DMSO ; 5mg
溶解性:Soluble in DMSO
纯度:HPLC≥98%
外观(性状):Light yellow to yellow Solid
储存条件:Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
靶点: AKT

产品详情

是一种 Akt 信号通路的有效抑制剂,具有抗癌和抗增殖活性。

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