産品簡介:
Cisplatin順鉑
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産品标簽
Cisplatin順鉑;Oxaliplatin奧沙利鉑;DNA Crosslinker DNA交聯劑;Cyclophosphamide環磷酰胺;CAS:15663-27-1;
産品信息
産品名稱
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産品編号
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CAS NO.
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規格
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價格(元)
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Cisplatin順鉑
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MZ3502-100MG
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15663-27-1
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100mg
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336
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Cisplatin順鉑
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MZ3502-1G
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15663-27-1
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1g
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1180
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Cisplatin順鉑
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MZ3502-5G
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15663-27-1
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5g
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3480
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産品描述
順鉑(Cisplatin),也稱順-二氯二氨基鉑(II)(cis-Diammineplatinum(II) dichloride),CAS NO. 15663-27-1,是一(yī)種基于鉑結構的強效抗腫瘤藥物(wù),一(yī)種烷化劑,與DNA形成細胞毒性加合物(wù),誘導鏈内和鏈間交聯,阻斷DNA複制和轉錄,最終引起凋亡。順鉑誘導p53依賴和非依賴機(jī)制的凋亡發生(shēng)。也能(néng)通(tōng)過活化caspase-3和X染色體連鎖凋亡抑制蛋白(bái)(XIAP)表達來誘導凋亡。鉑化的DNA加合物(wù)能(néng)夠加強喜樹堿對DNA拓撲異構酶的破壞作用。順鉑通(tōng)過激活巨噬細胞和免疫系統其它細胞來刺激免疫反應。體外順鉑處理的巨噬細胞具有提高(gāo)的抗原遞呈功能(néng)。單一(yī)或聯合使用順鉑,能(néng)夠用來治療幾種癌症,包括睾丸癌,卵巢癌,宮頸癌,膀胱癌和肺癌。
産品特性
1.CAS NO:15663-27-1
2.化學名:(SP-4-2)-diamminedichloro-platinum
3.别名:cis-Diammineplatinum(II) dichloride;cis-Diamminedichloroplatinum;Cisplatinum;CDDP;NSC 119875;順-二氯二氨基鉑(II);順式-二胺二氯鉑;順氯氨鉑;
4.分子式:Cl2H6N2Pt
5) 分子量:300.05 g/mol
6) 純度:98.0~102.0%
7) 外觀:黃色至橙色粉末
8) 溶解性:溶于DMSO(25mg/ml),DMF(10mg/ml),H2O(1.5mg/ml,微熱助溶)
9) 化學結構圖:
保存與運輸方法
保存:室溫避光(guāng)幹燥保存,也可置于+4ºC避光(guāng)幹燥長(cháng)期保存,至少2年(nián)有效。
運輸:室溫運輸。
注意事(shì)項
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鉑類抗腫瘤化合物(wù)如順鉑,奧沙利鉑,雖能(néng)溶于DMSO,但有文獻報(bào)道DMSO會(huì)使鉑類化合物(wù)失活,因此條件(jiàn)允許情況,建議使用其他溶劑,如DMF,細胞培養體系中DMF的終濃度最好少于0.1%,不能(néng)高(gāo)于1%。【文獻信息】:Hall MD, et al. Say no to DMSO: dimethylsulfoxide inactivates cisplatin, carboplatin, and other platinum complexes. Cancer Res. 2014 Jul 15;74(14):3913-22.
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本順鉑不是臨床藥物(wù),隻能(néng)用于科研用途,不能(néng)用于診斷或臨床用途。
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為(wèi)了您的安全和健康,請穿實驗服并戴一(yī)次性手套操作。
使用方法【源自(zì)文獻,僅作參考】
文獻1,Vencappa S, et al.Cisplatin induced sensory neuropathy is prevented by vascular endothelial growth factor-A. Am J Transl Res. 2015 Jun 15;7(6):1032-44. eCollection 2015. PMID: 26279748
體内研究(動物(wù)模型):
動物(wù)模型(Animal Model):Adult C57bl6 male (~30 g, 10 total) mice
實驗方法(Assay):All treatments administered were given via intraperitoneal (i.p.) injection. Treatments were biweekly i.p. injections of either vehicle (phosphate buffered saline) or cisplatin (2 mg/kg).
實驗結果(Result):Cisplatin induces neuropathic pain behaviour.Intraperitoneal administration of cisplatin (biweekly 2 mg/kg) to adult male mice led to a significant reduction in mechanical nociceptive withdrawal threshold indicative of mechanical allodynia and decrease in withdrawal latency to heat (heat hyperalgesia) versus the control group (i.p. vehicle) (n = 5 per group).
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Heidemann HT et al. Effect of aminophylline on cisplatin nephrotoxicity in the rat. Br J Pharmacol. 1989 Jun;97(2):313-8. PMID: 2758217
體内研究(動物(wù)模型):
動物(wù)模型(Animal Model):Male Wistar rats weighing 200-280g
實驗方法(Assay):Rats received cisplatin, 5 mg/kg intravenously. Vehicle-cisplatin rats were injectedwith an equal amount of normal saline. Kidney function was measured 5 days after drug administration.
實驗結果(Result):Intravenous cisplatin administration caused acute renal failure in all rats. The serum creatinine concentration was significantly increased in comparison to vehicle controls and the body weight was significantly reduced.
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— —Written/Edited by V. Shallan【版權歸MKBio懋康所有】
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