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Cyclophosphamide
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Cyclophosphamide图片
CAS NO:50-18-0
包装:50mg, 100mg, 200mg, 500mg
包装与价格:
包装价格(元)
50mg电议
100mg电议
200mg电议
500mg电议

产品介绍

生物活性

Cyclophosphamide是一种氮芥类烷化剂,使烷基连接到DNA的鸟嘌呤碱基。Cyclophosphamide inhibits the AChE reversibly with an IC50 of 511 microM. The Michaelis-Menten constant (Km) was 132 microM for AChE in the control system; a value increased by 78% in the CP treated system. The Vmax was 73.8 mumol/h/mg protein for the control system. Cyclophosphamide is used to treat cancers and autoimmune disorders. Cyclophosphamide belongs to a group of drugs called alkylating agents. It works by sticking to one of the cancer cell's DNA strands. DNA is the genetic code that is in the heart of all animal and plant cells. It controls everything the cell does.The cell cannot then divide into 2 new cells.

该产品在溶液状态不稳定,建议您现用现配,即刻使用。


化学数据

分子量261.09
分子式C7H15Cl2N2O2P
CAS号50-18-0
纯度>98%
溶解性(25°C)DMSO 35 mg/mL
Water 30 mg/mL
储存和运输条件2-8°C
常温运输及临时存放

实验操作 来自于公开的文献,仅供相同实验参考(如实验材料、目的不同,请参考其他文献)

细胞实验
细胞系CD4+ T-cell
方法Total CD4+ T cells, labeled with αCD25 BV605, were cultured for 3 days in RPMI/10% AB containing 0 or 50 IU/mL IL-2 as indicated, in presence of CPA (0 μM-1000 μM), mafosfamide (MAF; stabilized active derivative of CPA) (0 μM, 1.2 μM, 12 μM), and/or verapamil (10 μM). Doses of CPA and MAF were titrated to identify doses discriminating sensitivity of Treg and non-Treg cell subsets.
浓度0 μM, 1.2 μM, 12 μM
处理时间3 d

动物实验
动物模型Sprague–Dawley rats
配制
剂量25mg/kg
给药处理i.v.

不同实验动物依据体表面积的等效剂量转换表(数据来源于FDA指南)

小鼠大鼠豚鼠仓鼠
重量 (kg)0.020.151.80.40.0810
体表面积 (m2)0.0070.0250.150.050.020.5
Km系数36128520
动物 A (mg/kg) = 动物 B (mg/kg) × 动物 B的Km系数
动物 A的Km系数

例如,依据体表面积折算法,将化合物用于小鼠的剂量20 mg/kg 换算成大鼠的剂量,需要将20 mg/kg 乘以小鼠的Km系数(3),再除以大鼠的Km系数(6),得到化合物用于大鼠的等效剂量为10 mg/kg。


储备液配制

以下数据基于产品分子量,对于特殊产品,请参照COA中的储备液配制条件和说明进行操作。

Concentration / Solvent Volume / Mass1 mg5 mg10 mg
1 mM3.8301 mL19.1505 mL38.301 mL
5 mM0.766 mL3.8301 mL7.6602 mL
10 mM0.383 mL1.915 mL3.8301 mL