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网站主页 化工产品目录 生物化工 抑制剂 细胞凋亡(Apoptosis) Caspase 激活剂 1-(3,4-二氯苄基)-1H-吲哚-2,3-二酮 化合物 Apoptosis Activator 2
  • 化合物 Apoptosis Activator 2|T1772|TargetMol

化合物 Apoptosis Activator 2|T1772|TargetMol

MDK83190
79183-19-0
463 5mg 起订
731 10mg 起订
1492 50mg 起订
上海 更新日期:2024-09-23

TargetMol中国(陶术生物)

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产品详情:

中文名称:
化合物 Apoptosis Activator 2
英文名称:
MDK83190
CAS号:
79183-19-0
品牌:
TargetMol
产地:
美国
保存条件:
Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
纯度规格:
98.67%
产品类别:
抑制剂
货号:
T1772

Product Introduction

Bioactivity

NameMDK83190
DescriptionMDK83190 (Apoptosis Activator 2) is a potent apoptosis activator, induceing caspase-3 activation, PARP cleavage, and DNA fragmentation .
Cell ResearchAll viable cells within the defined field of a microscope reticle grid are counted using a manual mechanical counter by an experimenter blinded to condition. Cells are scored viable on the basis of both positive staining with the vital dye calcein acetoxymethyl ester and the morphological criterion of a smooth, spherical soma. Counts of viable cells are made in four non-overlapping fields per culture well with each condition represented by 3 separate wells. The number of viable cells counts per well for vehicle-treated control conditions ranged from 100-200. All experiments are repeated in at least 3 independent culture preparations. Raw cell count data are statistically analyzed with one-way ANOVA, followed by between group comparisons using the Fisher LSD test (significance indicated by P < 0.05). Cell viability is presented graphically as a percentage of live cells in the vehicle-treated control condition.(Only for Reference)
Kinase AssayCell-Free Apoptosis Assay: HeLa cell cytoplasmic extracts are prepared according to previously published reports. Apoptosis Activator 2 in DMSO are distributed into 96-well microtiter plates at a final concentration of 1 mM (final DMSO concentration is 1% vol/vol). To each well is added 250 μg of total protein from cytoplasmic extracts in HEB buffer (50 mM Hepes, pH 7.4/50 mM KCl/5 mM EGTA/2 mM MgCl), with 2 mM DTT, 2 μM cyto c, and 0.5 μM DEVD-AFC (Asp-Glu-Val-Asp-7-amino-4-trifluoromethylcoumarin) substrate in a total of 150 μL. Plates are incubated at 37 ℃, and fluorescence is read in a LJL Biosystems plate reader at 10-min intervals.
In vitroApoptosis Activator 2 (20 μM) 在降低的cyto c浓度下,将Apaf-1在细胞凋亡体中的比例增加1.5倍至33%。同时,该化合物在降低的cyto c水平和caspase-3激活水平下,使caspase-3活化程度增加4倍。Apoptosis Activator 2强烈诱导caspase-3活化、PARP裂解和DNA片段化,最终以4 μM的IC50杀死细胞。Apoptosis Activator 2诱导PBL、HUVEC、Jurkat、Molt-4、CCRF-CEM、BT-549、MDA-MB-468和NCI-H23细胞凋亡,其IC50分别为50 μM、43 μM、4 μM、6 μM、9 μM、20 μM、44 μM和35 μM。在48个测试的肿瘤细胞系中,Apoptosis Activator 2对绝大多数肿瘤细胞系展现出细胞静态效应,以10 μM的浓度在40个细胞系中抑制细胞生长50-100%。[1] Apoptosis Activator 2通过触发细胞凋亡体的形成引起细胞死亡。En1表达水平对Apoptosis Activator 2处理的腹侧中脑培养存活率无显著影响(-8.1 ± 6.0%)。如果使用其他三种试剂,存活率也没有显著变化(-10.7 ± 4.7%)。[2] Apoptosis Activator 2(10 μM)通过诱导凋亡DNA梯度和Tunel实验评估,在AGS细胞中诱导凋亡,并增强了抗TROP2偶联脂质体的凋亡诱导作用。[3] Cyclohexamide(10 μg/mL)或zVAD(50 μM)显著保护神经细胞培养物免受Apoptosis Activator 2的毒性。Apoptosis Activator 2(3 μM)导致大量神经元出现细胞死亡涉及的凝集核。DHT(10 nM)或E2(10 nM)显著保护神经细胞培养物免受Apoptosis Activator 2的毒性。[4]
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility InformationDMSO : 4.5 mg/mL (14.7 mM), Sonication is recommended.
Ethanol : 1.5 mg/mL (5 mM)
KeywordsInhibitor | MDK83190 | Apoptosis | MDK-83190 | inhibit | MDK 83190
Inhibitors RelatedLidocaine hydrochloride | Metronidazole | 5-Fluorouracil | Stavudine | Tributyrin | Dextran sulfate sodium salt (MW 4500-5500) | Myricetin | Sorafenib | L-Ascorbic acid | Acetylcysteine | Sodium 4-phenylbutyrate | Kaempferol
Related Compound LibrariesPyroptosis Compound Library | Bioactive Compound Library | Anti-Cancer Compound Library | Bioactive Compounds Library Max | Autophagy Compound Library | Apoptosis Compound Library | NO PAINS Compound Library | Anti-Neurodegenerative Disease Compound Library | Covalent Inhibitor Library | Target-Focused Phenotypic Screening Library
Apoptosis Activator 2|TargetMol

公司简介

上海陶术生物科技有限公司为美国Target Molecule Corp. ( Target Mol ) 在上海建立的全资子公司。我们与美国波士顿、德国慕尼黑的同事一起,为北美、欧洲和亚洲从事药物研发和生物学研究的科学家提供优质的产品和专业的服务。公司下设筛选事业部,化学事业部,生物事业部和新材料部。 从虚拟筛选到实体化合物分子供应;从商业化产品销售到个性化定制合成;从对明确靶点的分子筛选到对明确分子的多靶点筛选,从高通量筛选到化学结构优化,我们都可以满足您的科研用品及技术服务的需求。 经过在中国市场五年的精心耕耘,我们已成为筛选化合物领域优秀的供应商,为超过五百家学校和各类企业提供了品质卓越的小分子化合物和药物筛

成立日期 (12年)
注册资本 566.2651万人民币
员工人数 100-500人
年营业额 ¥ 1亿以上
经营模式 贸易,试剂,定制,服务
主营行业 化学试剂,生物活性小分子

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