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Elacridar

(別名: GF120918; GW0918; GG918; GW120918)
31 Cited Publications
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Based on 31 publication(s) in Google Scholar

Elacridar is an orally active P-glycoprotein (Pgp) and breast cancer resistance protein (BCRP) inhibitor. Elacridar can be used to examine the influence of efflux transporters on agent distribution to brain and the research of cancer.

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  • 純度: 99.66%
  • CAS 番号: 143664-11-3
  • 分子式: C34H33N3O5
  • 分子量:563.64
  • 保管条件:
    Powder   -20°C, 3 years , 4°C, 2 years ; In solvent   -80°C, 2 years , -20°C, 1 year
  • Elacridar Chemical Structure
    Elacridar 構造式
  • Experimental Validation Results for Elacridar
  • Experimental Validation Results for Elacridar
  • Experimental Validation Results for Elacridar
  • Experimental Validation Results for Elacridar
  • Experimental Validation Results for Elacridar
  • Experimental Validation Results for Elacridar
  • Experimental Validation Results for Elacridar
  • Experimental Validation Results for Elacridar
  • Experimental Validation Results for Elacridar
CAS 番号: 143664-11-3
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最寄りの代理店をお探しください Your local distributor: Hycultec GmbHHycultec
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  • Elacridar Chemical Structure
    Elacridar Chemical Structure
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    Elacridar purchased from MedChemExpress. Usage Cited in: Cancer Lett. 2024 Nov 25:217355. [Abstract]

    Customer Validation
     ABCB1 inhibition significantly reduced the number of 22Rv1-DR PCa cell-derived colonies compared to docetaxel treatment alone. Treatment with 2 μM Elacridar as a single agent did not impact colony growth in DR cells.

  • 1/16

    Elacridar purchased from MedChemExpress. Usage Cited in: Sci Adv. 2023 Oct 20;9(42):eabp9530. [Abstract]

    Customer Validation
     Elacridar (200 nM) increased the sensitivity of BCBM organoids to doxorubicin by immunofluorescent staining.

  • 1/16

    Elacridar purchased from MedChemExpress. Usage Cited in: Mol Psychiatry. 2023 Sep;28(9):3930-3942. [Abstract]

    Customer Validation
     Systemic ivabradine administration (0,3,10 mg/kg; i.p.) following Elacridar hydrochloride (5 mg/kg; i.v.; single dose), dose-dependently decreased the mean number of active lever presses and cocaine infusions under an FR2 reinforcement schedule.

  • 1/16

    Elacridar purchased from MedChemExpress. Usage Cited in: Antiviral Res. 2021 Sep:193:105124. [Abstract]

    Customer Validation
     Elacridar (0-33.34 μM, 72 h) do not induce cell toxicity by MTT assay.

  • 1/16

    Elacridar purchased from MedChemExpress. Usage Cited in: Int J Mol Sci. 2019 Mar 5;20(5). pii: E1125. [Abstract]

    Customer Validation
     Sensitization of resistant cells to chemotherapy by Elacridar (5 μM) treatment.

  • 1/16

    Elacridar purchased from MedChemExpress. Usage Cited in: J Mater Chem B. 2018 Dec 7;6(45):7521-7529. [Abstract]

    Customer Validation
     Elacridar hydrochloride (0.25 mg/kg; i.v.; every two days for a total of five doses). Ex vivo histological analyses of tumor sections excised from mice bearing MCF-7/ADR tumors after treatment. Nuclei were stained blue, and the extracellular matrix and cytoplasm were stained red through respectively. H&E staining images of the heart of MCF-7/ADR tumor-bearing mice after treatment. Scale bars represent 50 μM.

  • 1/16

    Elacridar purchased from MedChemExpress. Usage Cited in: J Mater Chem B. 2018 Dec 7;6(45):7521-7529. [Abstract]

    Customer Validation
     Bioactivity inhibition of the P-gp protein in MCF-7/ADR cells using the immunofluorescence assay after incubation with different samples. Green fluorescence: P-gp proteins labelled with FITC-antibody; blue fluorescence: nuclei stained with DAPI. The scale bars represent 20 mm. DOX concentration if applied: 10 mg/mL; Elacridar hydrochloride concentration if applied: 0.5 mg/mL.

  • 1/16

    Elacridar purchased from MedChemExpress. Usage Cited in: J Mater Chem B. 2018 Dec 7;6(45):7521-7529. [Abstract]

    Customer Validation
     Elacridar hydrochloride (0.25 mg/kg; i.v.; every two days for a total of five doses) co-delivered with DOX, exhibited a synergistic anticancer effect on multidrug-resistant MCF-7/ADR tumors in xenograft mouse models.

  • 1/16

    Elacridar purchased from MedChemExpress. Usage Cited in: J Drug Target. 2016;24(5):441-9. [Abstract]

    Customer Validation
     Cells are co-treated with 5 μM of free LY139481 or an equivalent dose of SMA-LY139481 and either vehicle control (0.01% DMSO), Elacridar (1 μM), KO143 (5 μM), Valspodar (1 μM) or a combination of efflux inhibitors for 6 h.

  • Elacridar