PCI-27483
目录号: PL08437 纯度: ≥99%
PCI-27483 是 FVIIa/tissue factor 抑制剂,具有抗肿瘤的活性。
CAS No. :871266-63-6
商品编号 规格 价格 会员价 是否有货 数量
PL08437-1mg 1mg ¥1607.00 请登录
PL08437-5mg 5mg ¥2893.00 请登录
PL08437-10mg 10mg ¥4821.00 请登录
PL08437-25mg 25mg ¥8036.00 请登录
PL08437-50mg 50mg ¥14465.00 请登录
PL08437-100mg 100mg ¥21216.00 请登录
PL08437-200mg 200mg 询价 询价
PL08437-500mg 500mg 询价 询价
PL08437-10mM*1mLinDMSO 10mM*1mLinDMSO ¥3796.00 请登录
Medlife所售产品仅用于科学研究(非临床研究),非药品不可食用,不可用于人体或动物的临床诊断和治疗,我们不为个人提供产品及服务。产品COA等资料,可至下方“质量控制”中下载。
中文名称
PCI-27483
中文别名
(S)-2-[[2-[5-(5-甲脒基-1H-苯并咪唑-2-基)-6,2'-二羟基-5'-氨基磺酰基联苯-3-基]乙酰基]氨基]琥珀酸;化合物PCI27483
英文名称
PCI-27483
英文别名
PCI-27483;(S)-2-[[2-[5-(5-Carbamimidoyl-1H-benzimidazol-2-yl)-6,2'-dihydroxy-5'-sulfamoylbiphenyl-3-yl]acetyl]amino]succinic acid;(S)-2-(2-(5-(5-carbamimidoyl-1H-benzo[d]imidazol-2-yl)-2',6-dihydroxy-5'-sulfamoylbiphenyl-3-yl)acetamido)succinic acid;PCI27483/PCI-27483;L-Aspartic acid, N-[2-[5-[6-(aminoiminomethyl)-1H-benzimidazol-2-yl]-5'-(aminosulfonyl)-2',6-dihydroxy[1,1'-biphenyl]-3-yl]acetyl];PCI27483;PCI 27483;CS-1599
Cas No.
871266-63-6
分子式
C26H24N6O9S
分子量
596.57
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
PCI-27483 是 FVIIa/tissue factor 抑制剂,具有抗肿瘤的活性。
生物活性
PCI-27483 is a FVIIa/tissue factor inhibitor, with antitumour effects.
性状
Solid
体外研究(In Vitro)
PCI-27483 inhibits the TF:FVIIa-complex induced phosphorylation of ERK1/2 and subsequent induction of c-fos in BxPC3 cells, a human pancreatic adenocarcinoma line that highly expresses TF. Furthermore, PCI-27483 blocks the TF:FVIIa induced secretion of IL8 in both BxPC3 cells and MDA-MB-231 breast cancer cells. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
PCI-27483 shows dose-dependent inhibition of thrombus formation, fibrin accumulation and PT. PCI-27483 (4 mg/kg) shows comparable anticoagulation effects as 2 mg/kg enoxaparin. PCI-27483 (0 and 90 mg/kg, s.c.) results in inhibition of tumor growth in CD1 nu/nu mice implanted with BxPC3 cells. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
ClinicalTrial
参考文献
[1]. Gómez-Outes A, et al. New parenteral anticoagulants in development. Ther Adv Cardiovasc Dis. 2011 Feb;5(1):33-59.
[2]. Julia Prescott, et al. PCI-27483, a small molecule inhibitor of Factor VIIa, inhibits growth of BxPC3 pancreatic adenocarcinoma xenograft tumors. Cancer Research May 2008 Volume 68, Issue 9 Supplement.
溶解度数据
In Vitro: DMSO : 62.5 mg/mL (104.77 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2