CAS 143664-11-3
:Elacridar
- 4-acridinecarboxamide, N-[4-[2-(3,4-dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)ethyl]phenyl]-9,10-dihydro-5-methoxy-9-oxo-
- Gf 120918
- Gf 129018
- Gg 918
- Gw 0918
- N-[4-[2-(3,4-Dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)ethyl]phenyl]-9,10-dihydro-5-methoxy-9-oxo-4-acridinecarboxamide
- N-{4-[2-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)ethyl]phenyl}-5-methoxy-9-oxo-9,10-dihydroacridine-4-carboxamide
- Elacridar
Elacridar
CAS :Formule :C34H33N3O5Degré de pureté :>98.0%(HPLC)Couleur et forme :White to Yellow to Green powder to crystalMasse moléculaire :563.65Elacridar
CAS :Formule :C34H33N3O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :563.6429Ref: IN-DA00AOQ8
1g582,00€5gÀ demander1mg49,00€25gÀ demander5mg52,00€10mg64,00€25mg102,00€50mg132,00€100mg156,00€250mg248,00€Elacridar
CAS :Formule :C34H33N3O5Degré de pureté :≥ 98.0%Couleur et forme :Off-white to yellow powderMasse moléculaire :563.64Elacridar
CAS :Elacridar (GG918) is a potent inhibitor of P-glycoprotein and BCRP.Cost-effective and quality-assured.Formule :C34H33N3O5Degré de pureté :98.12% - >99.99%Couleur et forme :SolidMasse moléculaire :563.64Elacridar
CAS :ElacridarFormule :C34H33N3O5Degré de pureté :By hplc: 100% (Typical Value in Batch COA)Couleur et forme : solidMasse moléculaire :563.64g/molElacridar
CAS :Inhibitor of ABC transporters; oral bioenhancer for anti-cancer therapyFormule :C34H33N3O5Degré de pureté :Min. 98 Area-%Couleur et forme :Yellow PowderMasse moléculaire :563.64 g/molElacridar - Bio-X ™
CAS :Elacridar is an inhibitor of ATP-dependent transport, which is mediated by P-glycoprotein (P-gp). Functioning as an oral bioenhancer, Elacridar addresses multiple drug resistance in tumors, a common challenge in cancer treatment often linked to changes in the expression of protein inhibitors. Inhibition of P-gp by Elacridar is a key mechanism behind its effectiveness. P-glycoprotein, a well-characterized human ABC transporter of the MDR/TAP subfamily, acts as an ATP-dependent efflux pump with broad substrate specificity. Its increased expression in the intestines can hinder drug absorption, leading to reduced bioavailability and inadequate therapeutic plasma concentrations. Elacridar addresses this challenge by inhibiting P-gp, thereby increasing the bioavailability of coadministered drugs. Overall, Elacridar emerges as a promising option for the treatment of solid tumors, offering a strategic approach to overcoming multidrug resistance in cancer therapy.
Formule :C34H33N3O5Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :563.64 g/molElacridar
CAS :Produit contrôléApplications A prototypical BCRP inhibitor. Inhibits the Bcrp1-mediated transport.
References Neville, K., et al.: Clin. Cancer Res., 10, 2525 (2004), Reardon, D., et al.: J. Clin. Oncol. 23, 9359 (2005), Pan, G., et al.: Drug Metab. Dispos., 35, 1165 (2007),Formule :C34H33N3O5Couleur et forme :NeatMasse moléculaire :563.64







