Bleomycin hydrochloride

CAS号

67763-87-5

分子式

C55H84ClN17O21S3(Average)

主要靶点

DNA/RNA Synthesis

仅限科研使用

Cat No : CM11042

Print datasheet

Synonyms

DNASynthesis|DNA Synthesis|DNA synthesis|Bleomycin Hydrochloride|Bleomycinhydrochloride|RNA Synthesis|RNASynthesis|盐酸博来霉素|盐酸博莱霉素|盐酸博莱霉素



产品信息

CAS号 67763-87-5
分子式 C55H84ClN17O21S3(Average)
主要靶点 DNA/RNA Synthesis
主要通路 细胞周期|DNA 损伤和修复
分子量 1451.01(Average)
纯度 , 此纯度可做参考,具体纯度与批次有关系,可咨询客服
储存条件 store at low temperature,keep away from direct sunlight | Shipping with blue ice.
别名 DNASynthesis|DNA Synthesis|DNA synthesis|Bleomycin Hydrochloride|Bleomycinhydrochloride|RNA Synthesis|RNASynthesis|盐酸博来霉素|盐酸博莱霉素|盐酸博莱霉素

体内活性

Bleomycin hydrochloride处理(3.5-4.0 mg/kg;气管内)小鼠体重至第4天减轻,然后至第7天开始增加,直至研究结束[3]。Bleomycin hydrochloride(3.5-4.0 mg/kg;气管内)显著增加肺部羟脯氨酸水平,并增加右侧尾肺叶质量[3]。Bleomycin hydrochloride(气管内给药;5.0 mg/kg/天)在约20-30 g的八周龄雄性BALB/c小鼠中诱发肺纤维化。Bleomycin上调α-SMA和Ⅰ型胶原的表达水平[4]。Bleomycin hydrochloride(气管内;2.5 mg/kg;1.25 mg/ml,约50 μl/只小鼠)在平均体重约24.5g的八周龄雄性C57BL/6小鼠中诱导肺纤维化[5]。

体外活性

Bleomycin hydrochloride 被认为是研究最为深入的人类淋巴细胞微核诱导剂,具有不同的遗传毒性机制。Bleomycin引起的DNA损伤主要是单链和双链断裂以及单个脱氧核酮糖/嘧啶位点损伤。同时,Bleomycin也是一种真正的辐射模拟化合物,几乎完全模拟了电离辐射的遗传效应[1]。Bleomycin hydrochloride对UT-SCC-19A细胞系的IC50值为4.0±1.3 nM。UT-SCC-12A和UT-SCC-12B对Bleomycin的抗性更强,其IC50值分别为14.2±2.8 nM和13.0±1.1 nM[2]。Bleomycin hydrochloride(50、100 μM;24、48小时)可诱导RLE-6TN细胞(50 μM)和A549细胞(100 μM)发生肺纤维化[4]。

溶解度

DMSO:45 mg/mL (31 mM);H2O:80 mg/mL (55.13 mM)

参考文献

1.Hovhannisyan G, et al. Comparative analysis of individual chromosome involvement in micronuclei induced by bleomycin in human leukocytes. Mol Cytogenet. 2016 Jun 21;9:49.
2.Jaaskela-Saari HA, et al. Squamous cell cancer cell lines: sensitivity to bleomycin and suitability for animal xenograft studies. Acta Otolaryngol Suppl. 1997;529:241-4.
3.Corboz MR, et al. Therapeutic administration of inhaled INS1009, a LRX-15 prodrug formulation, inhibits bleomycin-induced pulmonary fibrosis in rats. Pulm Pharmacol Ther. 2018 Apr;49:95-103.
4.Kang Miao, et al. Scutellarein inhibits BLM-mediated pulmonary fibrosis by affecting fibroblast differentiation, proliferation, and apoptosis. Ther Adv Chronic Dis. 2020 Jul 30;11:2040622320940185.
5.Ling Peng, et al. Scutellarin ameliorates pulmonary fibrosis through inhibiting NF-κB/NLRP3-mediated epithelial-mesenchymal transition and inflammation. Cell Death Dis. 2020 Nov 13;11(11):978.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
=
×
×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
×
=
×
C1   V1   C2   V2