For R&D use only.

GSK 269962

  • Catalog NO.:A863729
  • CAS No. : 850664-21-0
  • Molecular Formula:C29H30N8O5
  • Molecular Weight: 570.60
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Product Details

CAS Number 850664-21-0 Appearance Off-white solid
Catalog Number A863729 MDL Number
Molecular Formula C29H30N8O5 Molecular Weight 570.60
Boiling Point Melting Point
Flash Point Density
Synonyms GSK 269962; GSK-269962; GSK269962A; GSK 269962A; GSK-269962A; GSK269962B;N-[3-[[2-(4-amino-1,2,5-oxadiazol-3-yl)-1-ethyl-1H-imidazo[4,5-c]pyridin-6-yl]oxy]phenyl]-4-[2-(4-morpholinyl)ethoxy]-benzamide;GSK269962A
Storage Condition Store in a tightly closed container,in a cool and dry place

Safety

GHS Pictogram
Signal Word Warning UN Number
Hazard Statements H302-H315-H319-H335 Class
Precautionary Statements P261-P305+P351+P338 Packing Group

Description

Elacridar, also known as GF120918A, is a P-glycoprotein (P-gp) inhibitor, and has been used both in vitro and in vivo as a tool inhibitor of P-glycoprotein (Pgp) to investigate the role of transporters in the disposition of various test molecules. In vitro, GF120918A demonstrated high plasma protein binding across species, although a definitive protein binding evaluation was precluded by poor recovery, particularly in buffer and in mouse, rat, and dog plasma. GF120918A did not demonstrate potent inhibition of several human cytochrome P450 enzymes evaluated in vitro, with IC(50) values well above concentrations anticipated to be achieved in vivo. Together, these data confirm the utility of GF120918A as a tool P-glycoprotein inhibitor in preclinical species and offer additional guidance on preclinical dose regimens likely to produce P-glycoprotein-mediated effects.

143851-98-3 (Elacridar HCl)

143664-11-3 (Elacridar)

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GSK 269962
GSK 269962; GSK-269962; GSK269962A; GSK 269962A; GSK-269962A; GSK269962B;N-[3-[[2-(4-amino-1,2,5-oxadiazol-3-yl)-1-ethyl-1H-imidazo[4,5-c]pyridin-6-yl]oxy]phenyl]-4-[2-(4-morpholinyl)ethoxy]-benzamide;GSK269962A