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DMBA

DMBA

产品编号 T36696   CAS 57-97-6

7,12-Dimethylbenz[a]anthracene (DMBA) is a polycyclic aromatic hydrocarbon (PAH) that has been found in tobacco smoke and diesel exhaust and has carcinogenic activity.1,2It undergoes metabolic activation by numerous enzymes, including the cytochrome P450 (CYP450) isoform CYP1B1, as well as microsomal epoxide hydrolase (mEH), producing a variety of reactive metabolites that form DNA adductsin vivo, and it has been commonly used to induce tumor formation in various rodent models.2,3,1DMBA increases proliferation and migration of, and induces epithelial-to-mesenchymal transition (EMT) in, MCF-10A breast cancer cells when used at a concentration of 5 μM.4It also has immunosuppressant activity, inhibiting proliferation of isolated mouse splenic B- and T cells stimulatedex vivowith LPS or concanavalin A , respectively, when administered at doses of 50 and 100 mg/kg.5Intragastric administration of DMBA (20 mg/animal) induces formation of mammary gland tumors in rats.6DMBA (50 μg/animal), in combination with phorbol 12-myristate 13-acetate , initiates papilloma formation in a rat two-stage model of skin carcinogenesis.7

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DMBA Chemical Structure
DMBA, CAS 57-97-6
规格 价格/CNY 货期 数量
100 mg ¥ 768 现货
250 mg ¥ 1,750 现货
500 mg ¥ 2,460 现货
1 g ¥ 4,420 35日内发货
药物设计专题培训
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
产品目录号及名称: DMBA (T36696)
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参考文献
产品描述 7,12-Dimethylbenz[a]anthracene (DMBA) is a polycyclic aromatic hydrocarbon (PAH) that has been found in tobacco smoke and diesel exhaust and has carcinogenic activity.1,2It undergoes metabolic activation by numerous enzymes, including the cytochrome P450 (CYP450) isoform CYP1B1, as well as microsomal epoxide hydrolase (mEH), producing a variety of reactive metabolites that form DNA adductsin vivo, and it has been commonly used to induce tumor formation in various rodent models.2,3,1DMBA increases proliferation and migration of, and induces epithelial-to-mesenchymal transition (EMT) in, MCF-10A breast cancer cells when used at a concentration of 5 μM.4It also has immunosuppressant activity, inhibiting proliferation of isolated mouse splenic B- and T cells stimulatedex vivowith LPS or concanavalin A , respectively, when administered at doses of 50 and 100 mg/kg.5Intragastric administration of DMBA (20 mg/animal) induces formation of mammary gland tumors in rats.6DMBA (50 μg/animal), in combination with phorbol 12-myristate 13-acetate , initiates papilloma formation in a rat two-stage model of skin carcinogenesis.7
分子量 256.34
分子式 C20H16
CAS No. 57-97-6

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

DMSO: 10 mg/mL

DMF: 20 mg/mL

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TargetMol Library Books参考文献

1. Rengarajan, T., Rajendran, P., Nandakumar, N., et al.Exposure to polycyclic aromatic hydrocarbons with special focus on cancerAsian Pac. J. Trop. Biomed.5(3)182-189(2015) 2. Csiszar, A., Balasubramanian, B., Tarantini, S., et al.Chemically induced carcinogenesis in rodent models of aging: Assessing organismal resilience to genotoxic stressors in geroscience researchGeroscience41(2)209-227(2019) 3. Huberman, E., Chou, M.W., and Yang, S.K.Identification of 7,12-dimethylbenz[a]anthracene metabolites that lead to mutagenesis in mammalian cellsProc. Natl. Acad. Sci. U.S.A.76(2)862-866(1979) 4. Kwon, Y.-J., Ye, D.-J., Baek, H.-S., et al.7,12-Dimethylbenz[α]anthracene increases cell proliferation and invasion through induction of Wnt/β-catenin signaling and EMT processEnviron. Toxicol.33(7)729-742(2018) 5. Gao, J., Lauer, F.T., Dunaway, S., et al.Cytochrome P450 1B1 is required for 7,12-dimethylbenz(a)-anthracene (DMBA) induced spleen cell immunotoxicityToxicol. Sci.86(1)68-74(2005) 6. Barros, A.C.S.D., Muranaka, E.N.K., Mori, L.J., et al.Induction of experimental mammary carcinogenesis in rats with 7,12-dimethylbenz(a)anthraceneRev. Hosp. Clin. Fac. Med. Sao Paulo59(5)257-261(2005) 7. V?h?tupa, M., Pemmari, T., Junttila, I., et al.Chemical-Induced Skin Carcinogenesis Model Using Dimethylbenz[a]Anthracene and 12-O-Tetradecanoyl Phorbol-13-Acetate (DMBA-TPA)J. Vis. Exp.154(2019)

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请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。

母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。

体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。

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Keywords

DMBA 57-97-6 Inhibitor inhibitor inhibit

 

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