首页 工具
登录
购物车
Procarbazine hydrochloride

Procarbazine hydrochloride

产品编号 T1488   CAS 366-70-1
别名: NSC-77213 HCl, 盐酸甲基苄肼, Procarbazine HCl

Procarbazine hydrochloride (NSC-77213 HCl) 是一种烷化剂,是甲基肼衍生物的盐酸盐,具有抗肿瘤和诱变活性。

TargetMol的所有产品和服务仅用于科学研究,不能被用于人体,我们也不向个人提供产品和服务。
Procarbazine hydrochloride Chemical Structure
Procarbazine hydrochloride, CAS 366-70-1
规格 价格/CNY 货期 数量
5 mg ¥ 123 现货
10 mg ¥ 165 现货
25 mg ¥ 253 现货
50 mg ¥ 359 现货
100 mg ¥ 519 现货
500 mg ¥ 1,260 现货
1 g ¥ 1,860 现货
1 mL * 10 mM (in DMSO) ¥ 283 现货
其他形式的 Procarbazine hydrochloride:
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
重组蛋白限时优惠
产品目录号及名称: Procarbazine hydrochloride (T1488)
点击图片重新获取验证码
选择批次  
纯度: 85.01%
TargetMol batch loading
更多批次查询请联系客服
生物活性
化学信息
存储 & 溶解度
参考文献
产品描述 Procarbazine hydrochloride (NSC-77213 HCl) is the hydrochloride salt of a methylhydrazine derivative with antineoplastic and mutagenic activities. Although the exact mode of cytotoxicity has not been elucidated, procarbazine, after metabolic activation, appears to inhibit the trans-methylation of methionine into transfer RNA (t-RNA), thereby preventing protein synthesis and consequently DNA and RNA synthesis. This agent may also undergo auto-oxidation, resulting in the formation of cytotoxic free radicals which damage DNA through an alkylation reaction.
体外活性 Procarbazine plus Cu(II) induce piperidine-labile and formamidopyrimidine-DNA glycosylase-sensitive lesions at the 5'-ACG-3' sequence, complementary to a hotspot of the p53 gene, and the 5'-TG-3' sequence. Procarbazine causes DNA damage through non-enzymatic formation of the Cu(I)-hydroperoxo complex and methyl radicals. [1] Procarbazine has a strong clastogenic effect in hematopoietic cells and is mutagenic in a variety organs after high dose treatment. [2]
体内活性 Procarbazine causes significant decrease in testicular and epididymal weight and a drastic reduction in haploid cells and spermatogenic arrest, demonstrating variation among the test golden hamster. [3] Procarbazine produces a dose-dependent potentiation of MAO A in brown adipose tissue, the elevation being more pronounced following monomethylhydrazine, with activity rising to 350% of that in control homogenates in rats. Procarbazine or monomethylhydrazine reduces metabolism of this amine by a similar degree as had been determined ex-vivo in blood vessel homogenates. [4] Procarbazine is mutagenic, clastogenic and teratogenic in a wide range of test systems of varying complexity and a wide-spectrum carcinogen in rodents and monkeys, causing tumours of the haemopoietic system, the mammary gland, the lung and the nervous system. Procarbazine in vivo undergoes a complex series of metabolic changes that result in the generation of a number of chemically reactive species, including methylating agents and free radicals. [5]
别名 NSC-77213 HCl, 盐酸甲基苄肼, Procarbazine HCl
分子量 257.76
分子式 C12H19N3O·HCl
CAS No. 366-70-1

存储

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

溶解度

H2O: 48 mg/mL (186.2 mM)

DMSO: 42 mg/mL(162.9 mM)

Ethanol: 22 mg/mL(85.4 mM)

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
H2O / DMSO / Ethanol 1 mM 3.8796 mL 19.3979 mL 38.7958 mL 96.9894 mL
5 mM 0.7759 mL 3.8796 mL 7.7592 mL 19.3979 mL
10 mM 0.388 mL 1.9398 mL 3.8796 mL 9.6989 mL
20 mM 0.194 mL 0.9699 mL 1.9398 mL 4.8495 mL
50 mM 0.0776 mL 0.388 mL 0.7759 mL 1.9398 mL
H2O / DMSO 100 mM 0.0388 mL 0.194 mL 0.388 mL 0.9699 mL

TargetMol Calculator计算器

摩尔浓度计算器
稀释计算器
配液计算器
分子量计算器
=
X
X
X
=
X
=
/
g/mol

输入分子式,点击计算,可计算出产品的分子量。

TargetMol Library Books参考文献

1. Ogawa K, et al. Mutat Res,2003, 539(1-2), 145-155. 2. Suzuki T, et al. Mutat Res,1999, 444(2), 269-281. 3. Weissenberg R, et al. Arch Androl,2002, 48(2), 91-100. 4. Holt A, et al. J Pharm Pharmacol,1995, 47(10), 837-845. 5. Pletsa V, et al. Carcinogenesis,1997, 18(11), 2191-2196.
Cyclophosphamide Oxaliplatin Streptozocin Ifosfamide Carmustine Carboplatin VAL-083 Semustine

相关化合物库

该产品包含在如下化合物库中:
抗癌临床化合物库 抗癌上市药物库 药物功能重定位化合物库 抗癌药物库 抗癌活性化合物库 上市药物库 抗癌化合物库 已知活性化合物库 药物片段库 经典已知活性库

TargetMol Calculator剂量换算

对于不同动物的给药剂量换算,您也可以参考 更多...

TargetMol Calculator 体内实验配液计算器

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。

第一步:请输入动物实验的基本信息
剂量
mg/kg
每只动物体重
g
给药体积
μL
动物数量
第二步:请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% ddH2O
计算 重置

技术支持

您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。

Keywords

Procarbazine hydrochloride 366-70-1 Cell Cycle/Checkpoint DNA Damage/DNA Repair DNA Alkylator/Crosslinker DNA/RNA Synthesis NSC-77213 HCl 盐酸甲基苄肼 Procarbazine HCl Inhibitor Procarbazine Hydrochloride Hodgkin's disease anticancer activity inhibit L1210 Procarbazine inhibitor

 

TargetMol Loading
陶术
生物
TargetMol®中国区唯一合作伙伴
点击进入陶术生物官网陶术生物
联系我们
400-820-0310

上海市静安区江场三路238号8楼