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(-)-Alkannin

(-)-Alkannin

产品编号 T4958   CAS 517-88-4
别名: Alkannin, 左旋紫草素, 紫草素, Shikonin

(-)-Alkannin (Shikonin) 是从紫朱草中发现的一种天然产物,具有抗癌活性,可抑制细胞周期,诱导细胞凋亡,用作食品着色剂,在 Rho 激酶途径中可改善肝脏炎症。

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(-)-Alkannin Chemical Structure
(-)-Alkannin, CAS 517-88-4
规格 价格/CNY 货期 数量
20 mg ¥ 360 现货
1 mL * 10 mM (in DMSO) ¥ 260 现货
其他形式的 (-)-Alkannin:
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
产品目录号及名称: (-)-Alkannin (T4958)
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纯度: 98.28%
纯度: 98.18%
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天然产物信息
生物活性
化学信息
存储 & 溶解度
TCMIP信息
参考文献
植物来源
结构类型
产品描述 (-)-Alkannin (Shikonin) is a natural red naphthoquinone pigment, has antimicrobial, anti-tumor, and anti-inflammatory effects; a purified shikonin preparation is widely used for the production of medicinals, cosmetics, and some food products; shikonin also enters into the antiinflammatory ointment and cream compositions used for the treatment of burns. It can suppress the cell viability, adhesion, invasion and migratory ability of MGC-803 cells through TLR2- or NF-κB-mediated pathway.
体外活性 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay was performed for cell viability and adhesion ability of MGC-803 cells. Cell scratch repair experiments were conducted for the determination of migration ability while transwell assay for cell invasion ability. Western blot analysis and real-time polymerase chain reaction assay were used for the detection of protein and mRNA expressions. Fifty per cent inhibitory concentration of Shikonin on MGC-803 cells was 1.854?μm. Shikonin (1?μm) inhibited significantly the adhesion, invasion and migratory ability of MGC-803 cells. Interestingly, Shikonin in the presence or absence of anti-Toll-like receptor 2 (TLR2) antibody (2?μg) and nuclear factor-kappa B (NF-κB) inhibitor MG-132 (10?μm) could decrease these ability of MGC-803 cells markedly, as well as the expression levels of matrix metalloproteinases (MMP)-2, MMP-7, TLR2 and p65 NF-κB. In addition, the co-incubation of Shikonin and anti-TLR2/MG-132 has a significant stronger activity than anti-TLR2 or MG-132 alone.
激酶实验 Histamine release from basophils stimulated with anti-IgE antibody was analyzed fluorimetrically. Syk and Lyn kinase activities were tested in Vitro with recombinant proteins and analyzed by off-chip mobility shift assay. Shikonin dose-dependently inhibited the histamine release from basophils induced by anti-IgE antibody (IC50 = 2.6 +/- 1.0 microM; mean +/- SEM). A search for the target(s) of Shikonin in the signal cascade of IgE-mediated activation showed that it strongly inhibits Syk (IC50 = 7.8 microM, in the recombinant kinase assay), which plays a pivotal role in the degranulation response. A less significant inhibition was found for Lyn, which phosphorylates FcepsilonRI-betagamma subunits and also Syk.
别名 Alkannin, 左旋紫草素, 紫草素, Shikonin
分子量 288.3
分子式 C16H16O5
CAS No. 517-88-4

存储

keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

DMSO: 50 mg/mL (173.43 mM)

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 3.4686 mL 17.343 mL 34.6861 mL 86.7152 mL
5 mM 0.6937 mL 3.4686 mL 6.9372 mL 17.343 mL
10 mM 0.3469 mL 1.7343 mL 3.4686 mL 8.6715 mL
20 mM 0.1734 mL 0.8672 mL 1.7343 mL 4.3358 mL
50 mM 0.0694 mL 0.3469 mL 0.6937 mL 1.7343 mL
100 mM 0.0347 mL 0.1734 mL 0.3469 mL 0.8672 mL
TCMIP相关数据
中药材来源及性味归经

中药材来源及性味归经

中药材名称 中药材拉丁名 归经
软紫草 Arnebiaeuchroma(Royle) Johnst. 心包, 肝

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TargetMol Library Books参考文献

1. Takano-Ohmuro H , Yoshida L S , Yuda Y , et al. Shikonin inhibits IgE-mediated histamine release by human basophils and Syk kinase activity[J]. Inflammation Research, 2008, 57(10):484-488. 2. Liu J P , Liu D , Gu J F , et al. Shikonin inhibits the cell viability, adhesion, invasion and migration of the human gastric cancer cell line MGC‐803 via the Toll‐like receptor 2/nuclear factor‐kappa B pathway[J]. Journal of Pharmacy & Pharmacology, 2015, 67(8):1143-1155. 3. Gara R K , Srivastava V K , Duggal S , et al. Shikonin selectively induces apoptosis in human prostate cancer cells through the endoplasmic reticulum stress and mitochondrial apoptotic pathway[J]. Journal of Biomedical Science, 2015, 22(1):26. 4. Qu D , Xu X , Zhang M , et al. Cbl participates in shikonin-induced apoptosis by negatively regulating phosphoinositide 3-kinase/protein kinase B signaling. Molecular Medicine Reports, 2015. 6. Xue W, et al. Alkannin Inhibited Hepatic Inflammation in Diabetic Db/Db Mice. Cell Physiol Biochem. 2018;45(6):2461-2470. 7. Xu J, Wang Q, Leung E L H, et al. Compound C620-0696, a new potent inhibitor targeting BPTF, the chromatin-remodeling factor in non-small-cell lung cancer[J]. Frontiers of Medicine. 2020, 14(1): 60-67.

TargetMol Library Books文献引用

1. Zhang Z Z, Wen C H, Jia M, et al. Alkannin exerts antitumor properties in cutaneous squamous cell carcinoma by inducing apoptosis and shifting the M1/M2 polarization of tumor‐associated macrophages by upregulating PTEN. The Kaohsiung Journal of Medical Sciences. 2022 2. Xu J, Wang Q, Leung E L H, et al. Compound C620-0696, a new potent inhibitor targeting BPTF, the chromatin-remodeling factor in non-small-cell lung cancer. Frontiers of Medicine. 2020, 14(1): 60-67.
Domatinostat GSK1904529A STF-118804 Rhapontin Diatrizoic Acid SW106065 Sulfasalazine BTT-3033

相关化合物库

该产品包含在如下化合物库中:
激酶抑制剂库 抗癌活性化合物库 抗癌化合物库 中药单体化合物库 中药抗炎分子库 神经再生化合物库 氧化还原化合物库 神经元分化化合物库 抗癌细胞代谢库 植物来源化合物库

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请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。

母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。

体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。

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您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。

Keywords

(-)-Alkannin 517-88-4 Apoptosis PI3K/Akt/mTOR signaling PI3K Inhibitor ()Alkannin Alkannin 左旋紫草素 紫草素 inhibit Shikonin ( ) Alkannin inhibitor

 

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