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Beta-Lapachone, 4707-32-8
  • 品牌:爱必信(absin)
  • 产地:中国
  • 货号:abs813518
  • cas:4707-32-8
  • 价格: ¥529/瓶
  • 发布日期: 2022-04-07
  • 更新日期: 2025-07-20
产品详请
产地 中国
品牌 爱必信(absin)
货号 abs813518
用途 见爱必信官网
英文名称 见爱必信官网
包装规格 5mg,5mg,5mg,5mg,10mg,10mg,10mg,10mg,20mg,20mg,20mg,20mg,50mg,50mg,50mg,50mg
纯度 >98%%
CAS编号 4707-32-8
别名 β-拉帕醌;ARQ-501;NSC-26326;NSC-629749;SL-11001;beta-lapachone
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抑制剂描述:

产品名称:Beta-Lapachone

产品别名:见爱必信官网

英文别名:Beta-Lapachone

靶点:Topoisomerase

CAS:4707-32-8

纯度:>98%

外观:见爱必信官网

保存方法:Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.

描述:

Beta-Lapachone是一种选择性的DNA topoisomerase I(DNA拓扑异构酶I)抑制剂,对DNA拓扑异构酶II或连接酶无抑制作用。Beta-Lapachone抑制DNA topoisomerase I诱导的DNA松弛,这种作用具有剂量依赖性。Beta-Lapachone (100 nM或更高)处理,与对照组相比,抑制95%以上Topo I DNA舒展活性。Beta-Lapachone(1-5 μM)作用于HL-60和三种前列腺癌(DU-145, PC-3, 和LNCaP)细胞,使细胞周期停滞在G0/G1期,并通过锁定Topo I在DNA上和阻止复制叉移动,而诱导细胞凋亡。

溶解性:Ethanol :12.1 mg/mL (50 mM)
DMSO :24.2 mg/mL (100 mM)

体外研究:

Beta-Lapachone inhibits DNA relaxation induced by DNA topoisomerase I in a dose-dependent manner. Treatment of beta-lapachone (100 nM or greater) results in >95% inhibition of Topo I DNA unwinding activity compared to the DMSO control. beta-lapachone (1-5 μM) causes a block in G0/G1 of the cell cycle and induces apoptosis by locking Topo I onto DNA and blocking replication fork movement in HL-60 and three human prostate cancer (DU-145, PC-3, and LNCaP) cells. Beta-Lapachone facilitates the migration of mouse 3T3 fibroblasts and human endothelial EAhy926 cells through different MAPK signaling pathways, and thus accelerates scrape-wound healing in vitro. In addition, beta-Lapachone inhibits purified recombinant IDO1 activity through uncompetitive inhibition with IC50 of 0.44 μM, and beta-lapachone also exhibits superior retention of intracellular IDO1 inhibitory activity with an IC50 of 1.0 μM, partially dependent on biotransformation by NQO1. Beta-lapachone induces programmed necrosis of NQO1+ cancer cells by NQO1-dependent reactive oxygen species (ROS) formation and PARP1 hyperactivation.

体内研究:Beta-lapachone treatment (50 mg/kg) leads to potent inhibition of in vivo tumor growth in a xenograft mouse model of human ovarian cancer, and the combination of beta-lapachone and taxol produces a synergistic induction of apoptosis. In normal and diabetic (db/db) mice, treatment of beta-lapachone results in a faster healing process than vehicle only.

产品信息订购:

  产品货号   产品名称   规格 价格 大包装及货期
  abs813518   Beta-Lapachone   5mg   529.00   立即咨询
  abs813518   Beta-Lapachone   10mg   655.00   立即咨询
  abs813518   Beta-Lapachone   20mg   1178.00   立即咨询
  abs813518   Beta-Lapachone   50mg   2292.00   立即咨询

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