貨號	規(guī)格	價格	上海	北京	武漢	南京
S82386-1mg	95.0%	￥790.00 S82386-1mg ￥790.00 現(xiàn)貨	8 8	-	-	-
S82386-5mg	95.0%	￥2950.00 S82386-5mg ￥2950.00 現(xiàn)貨	6 6	-	-	-
S82386-10mg	95.0%	￥4700.00 S82386-10mg ￥4700.00 現(xiàn)貨	5 5	-	-	-

產(chǎn)品介紹

Valspodar (PSC 833) is a selective P-glycoprotein inhibitor that has been used as an experimental cancer treatment and chemosensitizer.

產(chǎn)品描述：

Valspodar (PSC 833) is a selective P-glycoprotein inhibitor that has been used as an experimental cancer treatment and chemosensitizer.

靶點：

P-glycoprotein;P-gp

體內(nèi)研究：

valspodar (10 mg/kg, o.p.) exhibits minimal blood-cell partitioning as reflected in its low mean blood-to-plasma ratio of approximately 0.52. Valspodar displays properties of slow clearance and a large volume of distribution. Valspodar shows properties of low hepatic extraction and wide distribution, similar to that of its structural analogue CsA. Preadministration of PSC833 to mice increases NSC 279836 fluorescent intensity in MDR tumor to 94% of that in the wild-type tumors

參考文獻：

1. Bajelan E, et al. Co-delivery of NSC 123127 and PSC 833 (Valspodar) by stealth nanoliposomes for efficient overcoming of multidrug resistance. J Pharm Pharm Sci. 2012 Sep;15(4):568-82. 2. PermissionsZ., et al. Pharmacokinetics of PSC 833 (valspodar) in its Cremophor EL formulation in rat.2010,40(1):55-61. 3. Fei Shen, et al. Dynamic Assessment of NSC 279836 Resistance and Modulation of Multidrug Resistance by Valspodar (PSC833) in Multidrug Resistance Human Cancer Cells. JPET August 2009,330 (2): 423-429

溶解性：

Soluble in DMSO

保存條件：

-20℃

配置溶液濃度參考：

	1mg	5mg	10mg
1 mM	0.823 ml	4.117 ml	8.233 ml
5 mM	0.165 ml	0.823 ml	1.647 ml
10 mM	0.082 ml	0.412 ml	0.823 ml
50 mM	0.016 ml	0.082 ml	0.165 ml

注意：

部分產(chǎn)品我司僅能提供部分信息，我司不保證所提供信息的權(quán)威性，僅供客戶參考交流研究之用。

參考文獻

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