貨號	規格	價格	上海	北京	武漢	南京
S81013-5mg	≥98%	￥425.00 S81013-5mg ￥425.00 現貨	8 8	-	-	-
S81013-10mg	≥98%	￥740.00 S81013-10mg ￥740.00 現貨	8 8	-	-	-
S81013-25mg	≥98%	￥1482.00 S81013-25mg ￥1482.00 現貨	8 0 8	-	-	-
S81013-50mg	≥98%	￥2409.00 S81013-50mg ￥2409.00 現貨	6 6	-	-	-
S81013-100mg	≥98%	￥3892.00 S81013-100mg ￥3892.00 現貨	5 5	-	-	-

產品介紹

Degrasyn (WP1130) is a cell-permeable deubiquitinase (DUB) inhibitor, directly inhibiting DUB activity of USP9x, USP5, USP14, and UCH37. Degrasyn has been shown to downregulate the antiapoptotic proteins Bcr-Abl and JAK2.

產品描述：

靶點：

IC50: 1.8 μM (Bcr-Abl, in K562, BV-173 cells):Deubiquitinase;Apoptosis;?JAK;?Bcr-Abl;?DUB;?Autophagy

體內研究：

Degrasyn suppresses the growth of K562 heterotransplanted tumors as well as both wild-type Bcr/Abl and T315I mutant Bcr/Abl-expressing BaF/3 cells transplanted into nude mice. To assess the possible therapeutic activity of Degrasyn against CML, nude mice received a subcutaneous transplant with K562 cells and are treated with 30 mg/kg Degrasyn every other day for 9 days after palpable tumor formation (10 days). This dose and schedule are well tolerated and effective in other tumor models. Antitumor activity is compared with that after daily Imatinib mesylate treatment (50 mg/kg). Nineteen days after tumor inoculation, tumors in the control group reached maximum allowable dimension, and the effect of therapy is assessed. Degrasyn treatment suppresses K562 tumor growth to an extent comparable to that observed in imatinib mesylate-treated animals, suggesting that Degrasyn is active in reducing the growth of established K562 tumors

參考文獻：

1. Bartholomeusz GA, et al. Activation of a novel Bcr/Abl destruction pathway by WP1130 induces apoptosis of chronic myelogenous leukemia cells. Blood. 2007 Apr 15;109(8):3470-8.

溶解性：

Soluble in DMSO

保存條件：

-20℃

配置溶液濃度參考：

	1mg	5mg	10mg
1 mM	2.602 ml	13.012 ml	26.023 ml
5 mM	0.52 ml	2.602 ml	5.205 ml
10 mM	0.26 ml	1.301 ml	2.602 ml
50 mM	0.052 ml	0.26 ml	0.52 ml

注意：

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

參考文獻

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