R1530
(Synonyms: 5-(2-氯苯基)-7-氟-1,2-二氢-8-甲氧基-3-甲基吡唑并[3,4-B][1,4]苯并二氮杂卓,R 1530;R-1530) 目录号 : GC12857
A multi-kinase inhibitor
Cas No.:882531-87-5
Sample solution is provided at 25 µL, 10mM.
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Quality Control & SDS
- View current batch:
- Purity: >99.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
R1530 is a potent and orally active inhibitor of mitosis/angiogenesis [1].
Mitosis is a part of the cell cycle process by which chromosomes in a cell nucleus are separated into two identical sets with each in its own nucleus. Angiogenesis refers to the growth of new blood vessels and is an essential component in the progression and metastasis of tumors [1].
R1530 showed potent inhibitory activities against cyclin-dependent kinases, such as CDK2 and CDK4, and angiogenesis-related growth factor receptor, such as KDR, FGFr, PDGFr, and EGFr [1]. In a series of human tumor cell lines, R1530 inhibited the growth of cells with IC50 values ranging from 0.22 to 3.43 μM. Also, R1530 strongly inhibited human umbilical vein endothelial cells (HUVEC) growth driven by VEGF or bFGF with IC50 values of 49 nM and 118 nM, respectively [2].
In nude mice bearing human H460 tumor xenografts, R1530 (3 to 25 mg/kg, orally twice a day, 20 days) inhibited tumor growth in a dose-dependent way. R1530 (the 25 mg/kg dose) reduced tumor size by 58% in average [3].
References:
[1]. Liu JJ, Higgins B, Ju G, et al. Discovery of a highly potent, orally active mitosis/angiogenesis inhibitor r1530 for the treatment of solid tumors. ACS Med Chem Lett, 2013, 4(2): 259-263.
[2]. Kolinsky K, Tovar C, Zhang YE, et al. Preclinical evaluation of the novel multi-targeted agent R1530. Cancer Chemother Pharmacol, 2011, 68(6): 1585-1594.
[3]. Tovar C, Higgins B, Deo D, et al. Small-molecule inducer of cancer cell polyploidy promotes apoptosis or senescence: Implications for therapy. Cell Cycle, 2010, 9(16): 3364-3375.
| Cas No. | 882531-87-5 | SDF | |
| 别名 | 5-(2-氯苯基)-7-氟-1,2-二氢-8-甲氧基-3-甲基吡唑并[3,4-B][1,4]苯并二氮杂卓,R 1530;R-1530 | ||
| 化学名 | 5-(2-chlorophenyl)-7-fluoro-8-methoxy-3-methyl-1,2-dihydropyrazolo[3,4-b][1,4]benzodiazepine | ||
| Canonical SMILES | CC1=C2C(=NC3=CC(=C(C=C3C(=N2)C4=CC=CC=C4Cl)F)OC)NN1 | ||
| 分子式 | C18H14ClFN4O | 分子量 | 356.78 |
| 溶解度 | DMF: 30 mg/mL,DMSO: 30 mg/mL,DMSO:PBS (pH 7.2) (1:7): 0.12 mg/mL,Ethanol: 20 mg/mL | 储存条件 | Store at -20°C |
| General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液；一旦配成溶液，请分装保存，避免反复冻融造成的产品失效。 储备液的保存方式和期限：-80°C 储存时，请在 6 个月内使用，-20°C 储存时，请在 1 个月内使用。 为了提高溶解度，请将管子加热至37℃，然后在超声波浴中震荡一段时间。 |
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| Shipping Condition | 评估样品解决方案：配备蓝冰进行发货。所有其他可用尺寸：配备RT，或根据请求配备蓝冰。 | ||
| 制备储备液 | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 2.8028 mL | 14.0142 mL | 28.0285 mL |
| 5 mM | 0.5606 mL | 2.8028 mL | 5.6057 mL |
| 10 mM | 0.2803 mL | 1.4014 mL | 2.8028 mL |
| 第一步：请输入基本实验信息（考虑到实验过程中的损耗，建议多配一只动物的药量） | ||||||||||
| 给药剂量 | mg/kg |  |
动物平均体重 | g | |
每只动物给药体积 | ul | |
动物数量 | 只 |
| 第二步：请输入动物体内配方组成（配方适用于不溶于水的药物；不同批次药物配方比例不同，请联系GLPBIO为您提供正确的澄清溶液配方） | ||||||||||
| % DMSO % % Tween 80 % saline | ||||||||||
| 计算重置 | ||||||||||
计算结果:
工作液浓度： mg/ml；
DMSO母液配制方法： mg 药物溶于 μL DMSO溶液（母液浓度 mg/mL，
体内配方配制方法：取 μL DMSO母液，加入 μL PEG300，混匀澄清后加入μL Tween 80，混匀澄清后加入 μL saline，混匀澄清。
1. 首先保证母液是澄清的；
2.
一定要按照顺序依次将溶剂加入，进行下一步操作之前必须保证上一步操作得到的是澄清的溶液，可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。