CP 100356 hydrochloride

Pricing Availability   Qty
说明: P-gp inhibitor
化学名: 4-(3,4-Dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)-N-2[2-(3,4-dimethoxyphenyl)ethyl]-6,7-dimethoxy-2-quinazolinamine hydrochloride
纯度: ≥98% (HPLC)
说明书
引用文献 (1)
评论
文献 (1)

生物活性 for CP 100356 hydrochloride

CP 100356 hydrochloride is a high affinity P-glycoprotein (P-gp) inhibitor (Ki values are 58 and 94 nM for mouse Pgp1a and Pgp1b isoforms). Inhibits calcein-AM uptake in MDR1-transfected MDCKII cells (IC50 = 0.5 μM) and prazosin transport in BCRP-transfected MDCKII cells (IC50 = 1.5 μM). Displays weak or no inhibitory activity against MRP1, OATP1B1 and several major human P450 enzymes (IC50 > 50 μM).

许可信息

Sold for research purposes under agreement from Pfizer Inc.

技术数据 for CP 100356 hydrochloride

分子量 597.1
公式 C31H36N4O6.HCl
储存 Desiccate at RT
纯度 ≥98% (HPLC)
CAS Number 142715-48-8
PubChem ID 71312025
InChI Key WWCHXVYTCMPAMV-UHFFFAOYSA-N
Smiles COC2=CC1=C(N3CCC(C=C(OC)C(OC)=C5)=C5C3)N=C(NCCC4=CC=C(OC)C(OC)=C4)N=C1C=C2OC.Cl

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

溶解性数据 for CP 100356 hydrochloride

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 11.94 20

制备储备液 for CP 100356 hydrochloride

以下数据基于产品分子量 597.1。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
0.2 mM 8.37 mL 41.87 mL 83.74 mL
1 mM 1.67 mL 8.37 mL 16.75 mL
2 mM 0.84 mL 4.19 mL 8.37 mL
10 mM 0.17 mL 0.84 mL 1.67 mL

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产品说明书 for CP 100356 hydrochloride

参考文献 for CP 100356 hydrochloride

参考文献是支持产品生物活性的出版物。

Taylor et al (1999) The equilibrium and kinetic drug binding properties of the mouse P-gp1a and P-gp1b P-glycoproteins are similar. Br.J.Cancer 81 783 PMID: 10555746

Wandel et al (1999) P-glycoprotein and cytochrome P-450 3A inhibition: dissociation of inhibitory potencies. Cancer Res. 59 3944 PMID: 10463589

Kalgutkar et al (2009) N-(3,4-dimethoxyphenethyl)-4-(6,7-dimethoxy-3,4-dihydroisoquinolin-2[1H]-yl)-6,7-dimethoxyquinazolin-2-amine (CP-100,356) as a "chemical knock-out equivalent" to assess the impact of efflux transporters on oral drug absorption in J.Pharm.Sci. 98 4914 PMID: 19373887


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关键词: CP 100356 hydrochloride, CP 100356 hydrochloride supplier, pfizer, CP100356, p-gp, p-glycoprotein, abcb1, atp, binding, cassette, multidrug, transporters, inhibitors, inhibits, Multidrug, Transporters, 4193, Tocris Bioscience

1 篇 CP 100356 hydrochloride 的引用文献

引用文献是使用了 Tocris 产品的出版物。 CP 100356 hydrochloride 的部分引用包括:

Sheehy et al (2015) Calcium and P-glycoprotein independent synergism between schweinfurthins and vera. Acta Neuropathol Commun 16 1259 PMID: 26046259


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