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  • 化合物 BMS 599626|T2610|TargetMol

化合物 BMS 599626|T2610|TargetMol

BMS-599626
714971-09-2
3900 10mg 起订
8920 25mg 起订
上海 更新日期:2024-09-29

TargetMol中国(陶术生物)

VIP3年
联系人:邵小姐
手机:4008200310 拨打
邮箱:marketing@tsbiochem.com

产品详情:

中文名称:
化合物 BMS 599626
英文名称:
BMS-599626
CAS号:
714971-09-2
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.
产品类别:
抑制剂
货号:
T2610

Product Introduction

Bioactivity

NameBMS-599626
DescriptionBMS-599626 (AC480) has been used in trials studying the treatment of Cancer, Metastases, and HER2 or EGFR Expressing Advanced Solid Malignancies.
Cell ResearchAll cell lines are maintained in RPMI 1640 supplemented with 10% fetal bovine serum, 100 units/mL penicillin, and 100 μg/mL streptomycin. Cells are plated at 1,000 per well in 96-well plates and are cultured for 24 hours before BMS-599626 is added. BMS-599626 is diluted in culture medium such that the final concentrations of DMSO are ≤ 1%. Following the addition of BMS-599626, the cells are cultured for an additional 72 hours before cell viability is determined by measuring the conversion of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide dye with the CellTiter96 kit. For some cell lines, there is a lack of a correlation between 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide dye metabolism and cell number, and a thymidine uptake assay is used to measure proliferation of these cell lines. Cells are plated in 96-well plates and treated with compounds as above. At the end of the 72-hour incubation, cells are pulsed with [3H]thymidine (0.4 μCi/well) for 3 hours before they are harvested. Cells are digested with 2.5% trypsin for 10 minutes at 37 °C and are harvested by filtration using a Packard Filtermate Harvester and GF/C Unifilter plates. Incorporation of radioactive thymidine into nucleic acids is determined by liquid scintillation counting.(Only for Reference)
Kinase AssayProtein kinase assays: The entire cytoplasmic sequences of HER1, HER2, and HER4 are expressed as recombinant proteins in Sf9 insect cells. HER1 and HER4 are expressed as fusion proteins with glutathione-S-transferase and are purified by affinity chromatography on glutathione-S-Sepharose. HER2 is subcloned into the pBlueBac4 vector and expressed as an untagged protein using an internal methionine codon (M687) for translation initiation. The truncated HER2 protein is isolated by chromatography on a column of DEAE-Sepharose equilibrated in a buffer that contains 0.1 M NaCl, and the recombinant protein is eluted with a buffer containing 0.3 M NaCl. For the HER kinase assays, reaction volumes are 50 μL and contains 10 ng of glutathione-S-transferase fusion protein or 150 ng of partially purified HER2. The mixtures also contains 1.5 μM poly(Glu/Tyr) (4:1), 1 μM ATP, 0.15 μCi [γ-33P]ATP, 50 mM Tris-HCl (pH 7.7), 2 mM DTT, 0.1 mg/mL bovine serum albumin, and 10 mM MnCl2. Reactions are allowed to proceed at 27°C for 1 hour and are terminated by the addition of 10 μL of a stop buffer (2.5 mg/mL bovine serum albumin and 0.3 M EDTA), followed by a 108-μL mixture of 3.5 mM ATP and 5% trichloroacetic acid. Acid-insoluble proteins are recovered on GF/C Unifilter plates with a Filtermate harvester. Incorporation of radioactive phosphate into the poly(Glu/Tyr) substrate is determined by liquid scintillation counting. Percent inhibition of kinase activity is determined by nonlinear regression analyses and data are reported as the inhibitory concentration required to achieve 50% inhibition relative to control reactions (IC50). Data are the averages of triplicate determinations. All other tyrosine kinases are also assayed using poly(Glu/Tyr) as a substrate. Kinetics of HER1 and HER2 inhibition are determined in reaction mixtures that contains varying concentrations of ATP and BMS-599626.
In vitro在体内,口服60 mg/kg到240 mg/kg范围的BMS-599626,导致剂量依赖性抑制 Sal2肿瘤生长,在其人乳腺肿瘤KPL-4异种移植物中产生有效的抗肿瘤活性最大耐受剂量为180 mg/kg,并且在其他HER2扩增异种移植模型以及其他HER1过表达异种移植模型中也具有类似的抗肿瘤活性.
In vivoMS-599626抑制表达高水平HER1和/或HER2的肿瘤细胞增殖,包括Sal2,BT474,N87,KPL-4,HCC202,HCC1954,HCC1419,AU565,ZR-75-30,MDA-MB-175,GEO和PC9细胞,IC50分别为0.24 μM,0.31 μM,0.45 μM,0.38 μM,0.94 μM,0.34 μM,0.75 μM,0.63 μM,0.51 μM,0.84 μM,0.90 μM和0.34 μM。BMS-599626选择性抑制重组HER1和HER2激酶的酶活性,IC50分别为20 nM和30 nM。BMS-599626通过促进周期重新分布和抑制DNA修复,显著增强了表达EGFR和Her2细胞的HN-5细胞的放射敏感性。此外,BMS-599626也抑制相关受体HER4,但是效力较低,IC50为190 nM。BBMS-599626不会明显抑制不表达HER1或HER2的卵巢肿瘤细胞系A2780和MRC5成纤维细胞的增殖。
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility InformationH2O : <1 mg/mL
DMSO : 104 mg/mL (196 mM)
Ethanol : 16 mg/mL (30.2 mM)
Keywordsantitumor | Epidermal growth factor receptor | Sal2 | inhibit | cells | ErbB-1 | AC-480 | proliferation | EGFR | KPL4 | GEO | AC 480 | Inhibitor | HER1 | cancer | autophosphorylation | BMS 599626 | BMS-599626 | selective | BMS599626
Inhibitors RelatedLidocaine hydrochloride | Lapatinib | Neratinib | Chalcone | Lidocaine | Gefitinib | Erlotinib | Osimertinib | Erlotinib hydrochloride | Lidocaine Hydrochloride hydrate | Genistein | Nintedanib
Related Compound LibrariesAnti-Ovarian Cancer Compound Library
AC480|TargetMol

公司简介

TargetMol Chemicals Inc. 总部位于马萨诸塞州波士顿,致力于为全球生化领域科学家的研究提供专业的产品和服务。TargetMol?品牌的客户群分布于40多个国家和地区,已发展成为全球知名的化合物库和小分子化合物研究供应商。 TargetMol?可提供160多种满足不同需求的化合物库,以及多种类型的生化试剂产品,包括12000多种抑制剂、16000多种天然产物和各类多肽、抗体、生命科学试剂盒等,此外,我们还建设有CADD(计算机辅助药物设计)研究中心、药理实验室、药化合成平台三大技术中心,全方位满足客户的定制需求。 凭借我们优质的产品和服务、快速高效的全球供应链和专业的技术支持,我们将有效帮助您缩短研发周期,取得更成功的结果。

成立日期 (12年)
注册资本 566.265100万人民币
员工人数 100-500人
年营业额 ¥ 1亿以上
经营模式 贸易,工厂,试剂,定制,服务
主营行业 天然产物,生化试剂,分子生物学,分子砌块,生物技术服务

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