Elacridar hydrochloride

Pricing Availability   Qty
说明: P-gp and BCRP inhibitor
别名: GF 120918
化学名: N-[4-[2-(3,4-Dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)ethyl]phenyl]-9,10-dihydro-5-methoxy-9-oxo-4-acridinecarboxamide hydrochloride
纯度: ≥98% (HPLC)
说明书
引用文献 (4)
评论 (1)
文献 (1)

生物活性 for Elacridar hydrochloride

Elacridar hydrochloride is a P-glycoprotein (P-gp/ABCB1) and breast cancer resistance protein (BCRP/ABCG2) inhibitor. Elacridar hydrochloride blocks P-gp-mediated multidrug resistance (MDR) of the cytotoxic drugs doxorubicin (Cat. No. 2252) and vincristine (Cat. No. 1257) in CHRC5 cells. Orally active.

许可信息

Sold for research purposes under agreement from GlaxoSmithKline.

技术数据 for Elacridar hydrochloride

分子量 600.1
公式 C34H33N3O5.HCl
储存 Store at -20°C
纯度 ≥98% (HPLC)
CAS Number 143851-98-3
PubChem ID 170320
InChI Key IQOJZZHRYSSFJM-UHFFFAOYSA-N
Smiles O=C1C3=C(C(C(NC4=CC=C(CCN5CC(C=C(OC)C(OC)=C6)=C6CC5)C=C4)=O)=CC=C3)NC2=C1C=CC=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 Elacridar hydrochloride

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 12 20

制备储备液 for Elacridar hydrochloride

以下数据基于产品分子量 600.1。 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 8.33 mL 41.66 mL 83.32 mL
1 mM 1.67 mL 8.33 mL 16.66 mL
2 mM 0.83 mL 4.17 mL 8.33 mL
10 mM 0.17 mL 0.83 mL 1.67 mL

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产品说明书 for Elacridar hydrochloride

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关键词: Elacridar hydrochloride, Elacridar hydrochloride supplier, GF120918, P-glycoprotein, P-gp, inhibitors, inhibits, multidrug, resistance, MDR, BCRP, ABCG2, ABCB1, GF, 120918, Multidrug, Transporters, 4646, Tocris Bioscience

4 篇 Elacridar hydrochloride 的引用文献

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

Ramesh et al (2014) Pro-inflammatory human Th17 cells selectively express P-glycoprotein and are refractory to glucocorticoids. J Exp Med 211 89 PMID: 24395888

Terrance G et al (2019) Lower Tubulin Expression in Glioblastoma Stem Cells Attenuates Efficacy of Microtubule-Targeting Agents. ACS Pharmacol Transl Sci 2 402-413 PMID: 32259073

Lahmann et al (2015) Systemic Administration of Glibenclamide Fails to Achieve Therapeutic Levels in the Brain and Cerebrospinal Fluid of Rodents. PLoS One 10 e0134476 PMID: 26225433

Jablonski et al (2014) Inhibiting drug efflux transporters improves efficacy of ALS therapeutics. Ann Clin Transl Neurol 1 996 PMID: 25574474


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1uM of elacridar is used to block the p glycoprotein.
By Shashirekha Shamamandri Markandaiah on 10/29/2018
分析类型: In Vitro
种属: Mouse
细胞系/组织: Endothelial cell, Astrocytes

Elacridar is used as P glycoprotein transporter blocker to enhance drug penetration in iPsc derived endothelial cell co cultured with ALS astrocytes.


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