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- 2025年12月05日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存：
货期：1-2天
- 供应商：
MedChemExpress LLC
- CAS号：
1604810-84-5
- 规格：
10 mM * 1 mL/1 mg/5 mg/10 mg
| 规格： | 10 mM * 1 mL | 产品价格： | ￥3300.0 |
|---|---|---|---|
| 规格： | 1 mg | 产品价格： | ￥891.0 |
| 规格： | 5 mg | 产品价格： | ￥2650.0 |
| 规格： | 10 mg | 产品价格： | ￥3950.0 |
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THZ2
CAS No. : 1604810-84-5
MCE 国际站：THZ2
产品活性：THZ2 是有效，选择性的 CDK7 抑制剂，IC50 值为 13.9 nM。
研究领域：Cell Cycle/DNA Damage
作用靶点：CDK
In Vitro: THZ2 selectively targets CDK7 and potently inhibits the growth of triple-negative but not ER/PR+ breast cancer cells. THZ2 at low nanomolar doses also efficiently suppresses the clonogenic growth of TNBC cells with IC50 of appr 10 nM. THZ2 induces apoptotic cell death in triple-negative but not ER/PR+ breast cancer cells or normal human cells.
In Vivo: THZ2 (10 mg/Kg) markedly reduces the growth rate of tumors in mice and demonstrates an anti-tumor activity. Compared to vehicle-treated tumors, tumor tissues isolated from mice treated with THZ2 has reduced proliferation and increased apoptosis, as indicated by immunostaining against Ki67 and cleaved Caspase 3 respectively. THZ2 in NOD-SCID mice leads to reduced body weight, suggesting that THZ2 mayt be less well-tolerated in this particular mouse strain.
相关产品：Covalent Screening Library Plus | Bioactive Compound Library Plus | Cell Cycle/DNA Damage Compound Library | Kinase Inhibitor Library | Anti-Cancer Compound Library | Anti-Aging Compound Library | Covalent Screening Library | Anti-Breast Cancer Compound Library | Anti-Blood Cancer Compound Library | Cancer Stem Cells Compound Library | Heterocyclic Compound Library | Membrane Protein-targeted Compound Library | Highly Selective Inhibitors Library | Serine/Threonine Kinase Inhibitor Library | Palbociclib | Abemaciclib | Ro-3306 | Ribociclib | Dinaciclib | GSK3326595 | THZ1 | Flavopiridol | SR-4835 | (R)-Roscovitine | THZ531 | AZD4573 | SY-5609 | Kenpaullone | Wogonin | SNS-032 | GSK 3 Inhibitor IX | Cirtuvivint | NVP-2 | Toyocamycin | Fadraciclib | Simurosertib | AT7519 | OTS964 hydrochloride | JNJ-7706621 | KB-0742 dihydrochloride | BSJ-4-116
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文献和实验wangch84 各位高手，兄弟最近忙于质粒构建，意图将一段长约4000 bp的片段，通过BamH1和EcoR1两个酶切位点连接到pcDNA3.1+载体上。情况如下： 1. 通过LA Taq酶扩增，并纯化回收目的片段（引物中带有酶切位点，保护性碱基＝3，上游带有Kozak序列）；由于回收效率很高，所以在进行下一步双酶切时只加了12 μl的目的片段，H2O 20 μl，10 X K BUFFER 4 μl，两种酶各2 μl，37℃作用过夜（12-14 h
-5.55.15.93.4-3.55.5-5.84.86.05.13.93.7-5.04.6-4.76.5-6.84.8-5.24.7-5.04.0-4.14.55.8-6.03.83-4.411.8-2.75.53.2-3.311.0-11.26.997.077.236.924.6-6.45.64.3-4.54.6-6.29.8-10.14.47-4.575.25.55.45.93.755.36.855.735.351.0左右8.14.97.8 4.584左右
项目正常值红细胞数（×1012/L）8.9（7.2-9.6）血细胞容量值（%）46（39-53）红细胞体积（μm3）55（52-58）白细胞（×1012/L）14（5-25）中性粒细胞（%）22（9-34）嗜酸粒细胞（%）2.2（0-6.0）嗜碱粒细胞（%）0.5（0-5.0）淋巴细胞（%）73（65-84）单核细胞（%）2.2（0-5.0）血小板（×109/L）1240（1100-1380）血红蛋白（g/L血液） （g/L血细胞）148（120-175） 320（300-350）
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