Salinomycin | MedChemExpress (MCE)-产品咨询-资讯-生物在线

Salinomycin | MedChemExpress (MCE)

作者:MedChemExpress LLC 暂无发布时间 (访问量:160)

MCE 的所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务。

Salinomycin

CAS No. : 53003-10-4

MCE 国际站:Salinomycin

产品活性:Salinomycin (Procoxacin),一种钾离子载体抗生素,选择性抑制革兰氏阳性菌的生长 (gram-positive bacteria)。Salinomycin 是 Wnt/β-catenin 信号传导的有效抑制剂,阻断 Wnt 诱导的 LRP6 磷酸化。Salinomycin (Procoxacin) 选择性抑制人肿瘤干细胞。

研究领域:Anti-infection  |  Stem Cell/Wnt  |  Autophagy  |  Apoptosis

作用靶点:Bacterial  |  Wnt  |  β-catenin  |  Mitophagy  |  Autophagy  |  Apoptosis  |  Antibiotic  |  Parasite

In Vitro: Salinomycin is a potent inhibitor of the Wnt signaling cascade. Incubation of the malignant lymphocytes with Salinomycin induces apoptosis within 48 h, with a mean IC50 of 230 nM. Salinomycin is also an antibiotic potassium ionophore, has been reported recently to act as a selective breast cancer stem cell inhibitor.
Salinomycin is a novel and an effective anticancer drug, inhibits SW620 cells and Cisp-resistant SW620 cells with IC50 of 1.54±0.23 μM and 0.32±0.05 μM, respectively. Salinomycin is found to have the ability to kill both cancer stem cells (CSCs) and therapy-resistant cancer cells. After continuous Salinomycin treatment for 48 h, the apoptotic cells are observed under the microscope and counted randomly at least 100 cells in one field. The number of apoptotic cells which are stained by Hoechst33342 is significantly increased in Cisp-resistant SW620 cells (20.20±3.72) than that of SW620 cells (9.40±2.07) per 100 cells (p<0.05). After treatment with Salinomycin for 48 h, flow cytometric analysis is used to detect the cell apoptosis both in SW620 cells and Cisp-resistant SW620 cells. The cell apoptotic rate in Cisp-resistant SW620 cells (37.82±3.63%) is significantly higher than that of SW620 cells (16.78±2.56%) (p<0.05).

In Vivo: After administration of 4 mg/kg Salinomycin (Sal), 8 mg/kg Salinomycin and 10 uL/g saline water for 6 weeks, the mice are sacrificed. The size of the liver tumors in the Salinomycin treatment groups diminishes compare with the control group. The mean diameter of the tumors decreases from 12.17 mm to 3.67 mm (p<0.05) and the mean volume (V=length×width2×0.5) of the tumors decreases from 819 mm3 to 25.25 mm3 (p<0.05). Next, the tumors are harvested, followed by HE staining, immunohistochemistry, and TUNEL assays, to assess the anti-tumor activity of Salinomycin. HE staining shows that the structure of the liver cancer tissue:nuclei of different sizes, hepatic cord structure is destroyed. Immunohistochemistry shows that PCNA expression is lower after Salinomycin treatment. HE staining and TUNEL assays indicates the Salinomycin-treated groups has higher apoptosis rates than control. Furthermore, immunohistochemistry shows an increased Bax/Bcl-2 ratio after Salinomycin treatment. The protein expression of β-catenin decreases in the Salinomycin treatment groups compared with control.
Salinomycin is a kind of monocarboxylic acid polyether type antibiotics, produced by the fermentation of Streptomyces albus, possesses a specific cyclic structure, and can form a complex compound with the pathogenic microorganisms and the extracellular cations of coccidian, especially K+, Na+, Rb+, to alter the intracellular and extracellular ion concentrations.

相关产品:Bioactive Compound Library Plus  |  Anti-Infection Compound Library  |  Apoptosis Compound Library  |  Stem Cell Signaling Compound Library  |  Wnt/Hedgehog/Notch Compound Library  |  Anti-Cancer Compound Library  |  Autophagy Compound Library  |  Anti-Aging Compound Library  |  Differentiation Inducing Compound Library  |  Antibacterial Compound Library  |  Cytoskeleton Compound Library  |  Antibiotics Library  |  Neuroprotective Compound Library  |  Anti-Breast Cancer Compound Library  |  Antiparasitic Compound library  |  Mitochondria-Targeted Compound Library  |  Transcription Factor-Targeted Library  |  Anti-Liver Cancer Compound Library   |  Rare Diseases Drug Library  |  Anti-Colorectal Cancer Compound Library   |  Human Metabolite Library  |  Anti-Prostate Cancer Compound Library  |  Anti-Pulmonary Fibrosis Compound Library  |  Cancer Stem Cells Compound Library  |  Heterocyclic Compound Library  |  Antihypertensive Compound Library  |  Membrane Protein-targeted Compound Library  |  Highly Selective Inhibitors Library  |  Highly Selective Activators Library  |  Cell Death Library  |  Extracellular Vesicles (EVs) Compound Library  |  Anti-Ovarian Cancer Compound Library  |  Multi-Target Compound Library  |  Radiosensitizer Library  |  Bioactive Compound Library Max  |  Anti-Gastric Cancer Compound Library  |  Anti-Fibrosis Compound Library  |  MG-132  |  Rapamycin  |  3-Methyladenine  |  Cycloheximide  |  Chloroquine  |  Dimethyl sulfoxide  |  Doxorubicin hydrochloride  |  Bafilomycin A1  |  Tamoxifen  |  Olaparib  |  Y-27632  |  Paclitaxel  |  Dexamethasone  |  Z-VAD-FMK  |  LY294002  |  2-Deoxy-D-glucose  |  Angiotensin II human  |  Acetylcysteine  |  Laduviglusib  |  Staurosporine  |  Actinomycin D  |  Puromycin dihydrochloride  |  SB-431542  |  5-Fluorouracil  |  Bortezomib  |  Oxaliplatin  |  Deferoxamine mesylate  |  Sorafenib  |  Trametinib  |  Gemcitabine

热门产品线:重组蛋白  |  药物筛选  |  天然产物  |  荧光染料  |  PROTAC  |  同位素标记物

Trending products:Recombinant Proteins  |  Bioactive Screening Libraries  |  Natural Products  |  Dye Reagents  |  PROTAC  |  Isotope-Labeled Compounds

品牌介绍:
•   MCE (MedChemExpress) 拥有200 多种全球独家化合物库,我们致力于为全球科研客户提供前沿最全的高品质小分子活性化合物;
•   50,000 多种高选择性抑制剂、激动剂涉及各热门信号通路及疾病领域;
•   产品种类涵盖各种重组蛋白,多肽,常用试剂盒 ,更有 PROTAC、ADC 等特色产品,广泛应用于新药研发、生命科学等科研项目;
•   提供虚拟筛选,离子通道筛选,代谢组学分析检测分析,药物筛选等专业技术服务;
•   设有专业的实验中心和严格的质控、验证体系;
•   提供 LC/MS、NMR、HPLC、手性分析、元素分析等各项质检报告,确保产品的高纯度、高品质;
•   产品的生物活性多经各国客户实验验证;
•   Nature, Cell, Science 等多种顶级期刊及制药专利收录了MCE客户的科研成果;
•   专业团队跟踪最新的制药及生命科学研究进展,为您提供全球最新的活性化合物;
•   与世界各大制药公司及知名科研机构建立了长期的合作。

类药多样性化合物库
顾客使用MCE产品发表的科研文献
一站式药筛新体验
MCE 您身边的生物活性分子大师 | 抑制剂、激动剂、化合物库
重组蛋白 | 高纯度、高稳定性
磁珠
MCE Hotline: 4008203792 | 中国现货 - 全球文献引用 - 高纯度高品质 - 全方位技术支持
MedChemExpress LLC 商家主页

地 址: 上海市浦东新区张衡路1999弄3号楼

联系人: 销售部

电 话: 021-58955995

传 真: 021-53700325

Email:sales@medchemexpress.cn

相关咨询
ADVERTISEMENT