Copy Link Print Information

Tariquidar dimesylate

(Synonyms: XR9576 dimesylate)
57 Cited Publications
고객리뷰

Based on 57 publication(s) in Google Scholar

Tariquidar dimesylate (XR9576 dimesylate) is a P-glycoprotein (P-gp) inhibitor. Tariquidar dimesylate increases the concentration of the drug in the brain by binding to P-glycoprotein, preventing it from transporting the drug from inside to outside the brain. Tariquidar dimesylate can be used in the study of blood-brain barrier penetration and multidrug resistance.

연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.

  • CAS No.: 625375-84-0
  • 화학식: C40H46N4O12S2
  • 분자량:838.94
  • 보관:

    Please store the product under the recommended conditions in the Certificate of Analysis.

  • Tariquidar dimesylate Chemical Structure
    Tariquidar dimesylate Chemical Structure
  • Experimental Validation Results for Tariquidar dimesylate
  • Experimental Validation Results for Tariquidar dimesylate
  • Experimental Validation Results for Tariquidar dimesylate
  • Experimental Validation Results for Tariquidar dimesylate
  • Experimental Validation Results for Tariquidar dimesylate
CAS No.: 625375-84-0
사이즈
가격
재고
수량
Amount: USD 0.00
Please select quantity
or
or

* 장바구니에 담기 전 물품의 수량을 선택해 주십시오.

To place orders, for customer services and technical support, please contact: MedChemExpress USA

Tel: 609-228-6898 E-mail: [email protected] [email protected]

Data Download
Other Forms of Tariquidar dimesylate:

To place orders, for customer services and technical support, please contact:

609-228-6898
[email protected] [email protected]
주변의 대리점 찾기 Your local distributor: Hycultec GmbHHycultec
  • Biological Activity
  • Chemical Information
  • 순도&문서
  • References
  • Help & FAQs
Top Publications Citing

Use of MCE Products

Publications Citing Use of MedChemExpress (MCE) Tariquidar dimesylate

More
Customer Validation & Images
In Vivo Efficacy StudyCell Proliferation/Viability AssayWBCell Imaging/StainingFlow Cytometry
  • In Vivo Efficacy Study
  • Cell Proliferation/Viability Assay
  • WB
  • Flow Cytometry
  • Cell Imaging/Staining
Keywords
MOQ
Minimum order quantity
100 mg

견적 받기 해외재고보유

Other size
견적 받기
Please select quantity
Amount: USD 0.00
Sign in to MedChemExpress 로그인
Register
Sign in to MedChemExpress
회원가입

At least 6 characters

Personalize your experience, you are currently not signed in. For a better experience, please create an online profile, you can:

Obtain points redemption prizes
Check out faster
Add multiple shipping locations
View orders
Assay Types
  • Tariquidar dimesylate Chemical Structure
    Tariquidar dimesylate Chemical Structure
    1/16
  • 1/16

    Tariquidar dimesylate purchased from MedChemExpress. Usage Cited in: Cell. 2023 Dec 7;186(25):5500-5516.e21. [Abstract]

    Customer Validation
     Survival curves of mice under SD (SR means 48 h of recovery after SD) with i.p. administration of tariquidar (n = 5) or vehicle (n = 5).

  • 1/16

    Tariquidar dimesylate purchased from MedChemExpress. Usage Cited in: Cell Death Discov. 2021 Aug 5;7(1):204. [Abstract]

    Customer Validation
     MCF-7ADR cells were treated with ADR (2μM) alone or together with Tariquidar (TQ; 0.5 μM) for 48h. Cell viability was detected using the CCK8 assays.

  • 1/16

    Tariquidar dimesylate purchased from MedChemExpress. Usage Cited in: Antioxidants (Basel). 2021 Jun 11;10(6):949. [Abstract]

    Customer Validation
     Tariquidar (1.5 μM; 72 h). Western blotting results show the specific inhibition of both MRP1/ABCC1 and MDR1/ABCB1 after tariquidar treatment for 72 h in both control and DEHP-exposed MDA-MB-231 clones.

  • 1/16

    Tariquidar dimesylate purchased from MedChemExpress. Usage Cited in: Antioxidants (Basel). 2021 Jun 11;10(6):949. [Abstract]

    Customer Validation
     Tariquidar (1.5 μM; 2 h). Enhanced Dox accumulation was observed following 2 h of Tariquidar pretreatment in DEHP-exposed MDA-MB-231 clones #1 and #2, analyzed by a BD Accuri TW C6 flow cytometer.

  • 1/16

    Tariquidar dimesylate purchased from MedChemExpress. Usage Cited in: Small. 2020 Nov;16(44):e2004172. [Abstract]

    Customer Validation
     In vitro tumor penetration of the DOX-loaded liposomes in BxPC3 MTS. The BxPC3 MTS were prestained with or without a Pg-p inhibitor Tariquidar (10 nM) for 3 h. Subsequently, the MTS were cultured with DOX-loaded liposomes for 6 h. The MTS were visualized using CLSM in Z-stacks with 25 µm intervals. DOX (red).

  • Tariquidar dimesylate