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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
4°C, protect from light
- 英文名:
Campathecin; (S)-(+)-Camptothecin; CPT
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
7689-03-4
- 规格:
10 mM * 1 mL/100 mg/500 mg/1 g/5 g
| 规格: | 10 mM * 1 mL | 产品价格: | ¥500.0 |
|---|---|---|---|
| 规格: | 100 mg | 产品价格: | ¥395.0 |
| 规格: | 500 mg | 产品价格: | ¥900.0 |
| 规格: | 1 g | 产品价格: | ¥1280.0 |
| 规格: | 5 g | 产品价格: | ¥2550.0 |
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Camptothecin
CAS No. : 7689-03-4
MCE 国际站:Camptothecin
产品活性:Camptothecin (CPT),一种生物碱,是一种 DNA topoisomerase I (Topo I) 抑制剂,其 IC50 值为 679 nM。Camptothecin (CPT) 对结直肠癌、乳腺癌、肺癌和卵巢癌具有强大的抗肿瘤活性,通过改变人类癌细胞中的 miRNA 表达模式来调节 hypoxia-inducible factor-1α (HIF-1α) 活性。
研究领域:Cell Cycle/DNA Damage | Antibody-drug Conjugate/ADC Related | Epigenetics | Apoptosis | Anti-infection
作用靶点:Topoisomerase | ADC Cytotoxin | MicroRNA | Influenza Virus | Apoptosis | Fungal | Antibiotic
In Vitro: High TOP1 enzymatic activity MCF7 (Luminal subtype) and HCC1419 (HER2 subtype) show high sensitivity toward Camptothecin (0.1 μM to 5 μM; 72 hours) treatment, exhibiting the IC50 values of 0.089 μM and 0.067 μM, respectively.
Camptothecin (0.5 μM; 6 and 24 hours) reduces desferrioxamine-activated VEGF expression.
Camptothecin (0.5 μM; 8 to 24 hours) strongly prevents the desferrioxamine-dependent HIF-1a accumulation.
In Vivo: Camptothecin (2 mg/kg every other day) treats mice, has developed numerous pulmonary metastases.
Treatment with both kinase inhibitor of nuclear factor-kappaB-1 (KINK-1) and Camptothecin led to a statistically significant reduction in the number of pulmonary metastases.
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文献和实验示例: Jurkat细胞用1μM喜树碱(Camptothecin) (左)或未加药 (右)处理4h,FITC-Annexin V/PI荧光双染细胞凋亡检测试剂盒染色后,流式细胞仪荧光检测。 Annexin V-FITC单阳性细胞为早期凋亡细胞,Annexin V-FITC和PI染色双阳性的细胞为坏死细胞或者晚期凋亡。PI单染色阳性位裸核细胞。 实测数据可能会因细胞类型、细胞凋亡情况,检测仪器等的不同而存在差异,图中数据仅供参考。 流式检测细胞凋亡的数据分析方法: 1) 选中所有颗粒,将FSC
iodide (P1304, P3566, P21493). The image was acquired using bandpass filters appropriate for fluorescein. Jurkat 人类白血病T细胞经1微升喜树碱处理,ps外翻,早期凋亡特异性的特征被annexin-5检测到。晚期凋亡和坏死细胞被pi染色。本图是由相应的荧光滤光片获取的。 HL-60 cells treated with camptothecin for three hours
重组人TFAR19蛋白对羟基喜树碱诱导人7721肝癌细胞凋亡的增敏作用
新的人凋亡相关基因产物TFAR19 蛋白对羟基喜树碱诱导人7721 肝癌细胞凋亡的增敏作用。 方法:将不同浓度的rhTFAR19 蛋白单独或与羟基喜树碱(hydroxy camptothecin , HCPT) 同时加入处于指数生长期的7721 肝癌细胞中共同培养,通过透射电镜、DNA 片段化分析、PI 及Annexin V 标记进行流式细胞仪分析,观察细胞的形态学和细胞凋亡的变化。 结果:不同质量浓度的rhTFAR19 蛋白单独作用于7721 肝癌细胞未见明显
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