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Cisplatin
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。
Cisplatin图片
CAS NO:15663-27-1
包装与价格:
包装价格(元)
100mg电议
500mg电议
1 g电议
5 g电议
10 g电议

产品名称
顺铂
cis-Platinum
CDDP
cis-Diaminodichloroplatinum
产品介绍
Cisplatin (CDDP) 是一种抗肿瘤的化疗剂,它与DNA交联引起癌细胞中 DNA 损伤。Cisplatin 可激活铁死亡 (ferroptosis) 并诱导自噬 (autophagy)。
生物活性

Cisplatin (CDDP) is an antineoplastic chemotherapy agent by cross-linking withDNAand causing DNA damage incancercells. Cisplatin activatesferroptosisand inducesautophagy[1][2][3].

IC50& Target

DNA Alkylator/Crosslinker[1]

体外研究
(In Vitro)

Cisplatin (CDDP) causes apoptosis of HeLa cells in a dose-dependent manner, with a concentration of 30 μM Cisplatin resulting in death of greater than 90% of the cell population by 24 h of treatment. The kinetics of Cisplatin-induced apoptosis are examined using a 30 μM concentration. Cisplatin Activates the MEK/ERK Signaling Pathway, 20 and 30 μM Cisplatin, both of which results in significant apoptosis, leads to strong activation of ERK[1].
Cisplatin (50 μM) produces time-dependent apoptosis in renal proximal tubular cell (RPTCs), causing cell shrinkage, a 50-fold increase in caspase 3 activity, a 4-fold increase in phosphatidylserine externalization, and 5- and 15-fold increases in chromatin condensation and DNA hypoploidy, respectively[2].

体内研究
(In Vivo)

In melanoma-bearing mice, Cisplatin (CDDP; 4 mg/kg B.W.) reduces the size and weight of the solid tumors, and HemoHIM supplementation with Cisplatin enhances the decrease of both the tumor size and weight[3].
Cisplatin administration results in significant increases in the kidney weight as a percentage of the total body weight, urine volume, serum creatinine, and blood urea nitrogen by about 132, 315, 797, and 556% in comparison with the control rats, respectively[4].

Clinical Trial
分子量

300.05

性状

Solid

Formula

Cl2H6N2Pt

CAS 号

15663-27-1

中文名称

顺铂

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

溶解性数据
In Vitro: 

DMF : 5 mg/mL(16.66 mM;Need ultrasonic;DMSO can inactivate Cisplatin's activity)

H2O : 1 mg/mL(3.33 mM;Need ultrasonic;DMSO can inactivate Cisplatin's activity)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM3.3328 mL16.6639 mL33.3278 mL
5 mM0.6666 mL3.3328 mL6.6656 mL
10 mM0.3333 mL1.6664 mL3.3328 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month (protect from light)。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: 0.5%CMC-Na/saline water

    Solubility: 20 mg/mL (66.66 mM); Suspended solution; Need ultrasonic

  • 2.

    请依序添加每种溶剂: 50%PEG300   50% saline

    Solubility: 10 mg/mL (33.33 mM); Suspended solution; Need ultrasonic

*以上所有助溶剂都可在本网站选购。