KGP94
目录号: PL15155 纯度: ≥99%
CAS No. :1131456-28-4
商品编号 规格 价格 会员价 是否有货 数量
PL15155-5mg 5mg ¥3585.45 请登录
PL15155-10mg 10mg ¥5316.36 请登录
PL15155-25mg 25mg ¥9520.00 请登录
PL15155-50mg 50mg ¥12981.82 请登录
PL15155-100mg 100mg 询价 询价
PL15155-200mg 200mg 询价 询价
PL15155-10mM*1mLinDMSO 10mM*1mLinDMSO ¥3944.00 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
KGP94
英文名称
KGP94
英文别名
KGP94;[(E)-[(3-bromophenyl)(3-hydroxyphenyl)methylidene]amino]thiourea;GTPL6533
Cas No.
1131456-28-4
分子式
C14H12BrN3Os
分子量
350.23
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
KGP94 是一种特异的 cathepsin L 抑制剂,IC50为 189 nM。KGP94 抑制转移癌的运动性和侵袭性,对人类细胞的毒性低 (GI50=26.9µM)。
生物活性
KGP94 is a selective inhibitor of cathepsin L with an IC 50 of 189 nM. KGP94 inhibits migration and invasion of metastatic carcinoma and shows low cytotoxicity (GI 50 =26.9 μM) against various human cell lines.
性状
Solid
IC50 & Target[1][2]
189 nM (cathepsin L)
体外研究(In Vitro)
KGP94 (10 or 20 μM, 24 h) reduces expression of M2 (macrophage) markers (Arginase-1 and CD206) and cells invasion of primary bone marrow-derived macrophages or Raw264.7.
KGP94 (25 μM, 24 h) impairs the incasive capacities of both prostate and breat cancer cells by 53% and 88%, respectively.
KGP94 (25 μM, 24 h) suppresses secreted CTSL activity by 94% and 92% in PC-3ML and MDA-MB-231, repsectively. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
KGP94 (i.p.; 20 mg/kg; once daily for 3 days) exhibits anti-metastatic and anti-bone resorptive efficacy in a prostate cancer bone metastasis model. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
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
参考文献
[1]. Parker EN, et al. Synthesis and biological evaluation of a water-soluble phosphate prodrug salt and structural analogues of KGP94, a lead inhibitor of cathepsin L. Bioorg Med Chem Lett. 2017 Mar 1. 27(5):1304-1310.
[2]. Munikishore R, et al. An efficient and concise synthesis of a selective small molecule non-peptide inhibitor of cathepsin L: KGP94. Bioorg Chem. 2021 Nov. 116:105317.
溶解度数据
In Vitro: DMSO : ≥ 100 mg/mL (285.53 mM)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