ChemicalBook--->CAS DataBase List--->365565-02-2

365565-02-2

365565-02-2 Structure

365565-02-2 Structure
IdentificationBack Directory
[Name]

PGP-4008
[CAS]

365565-02-2
[Synonyms]

Abcb1b
PGP-4008
PGP-4408
Mdr1b Rat
Mdr1b Rat Vesicular Transport Kit
rodent multidrug resistance protein
Recombinant Human p-Glycoprotein/MRP
N-(1-BENZYL-2,3-DIHYDRO-1H-PYRROLO[2,3-B]QUINOLIN-4-YL)-2-PHENYLACETAMIDE
Benzeneacetamide, N-[2,3-dihydro-1-(phenylmethyl)-1H-pyrrolo[2,3-b]quinolin-4-yl]-
[Molecular Formula]

C26H23N3O
[MDL Number]

MFCD03452998
[MOL File]

365565-02-2.mol
[Molecular Weight]

393.48
Chemical PropertiesBack Directory
[storage temp. ]

−20°C
[solubility ]

DMSO: 50mM; Ethanol: 5mM
[form ]

White to off-white powder.
[color ]

White to off-white
Safety DataBack Directory
[Hazard Codes ]

T
[Risk Statements ]

45-21/22-34-37-52/53
[Safety Statements ]

22-24/25-61-45-36/37/39-26-53
[WGK Germany ]

3
[HS Code ]

3504009000
Hazard InformationBack Directory
[Description]

PGP-4008 is a selective inhibitor of P-glycoprotein (P-gp) that does not affect the activity of multidrug resistance-related protein 1 (MRP1). It is effective in vitro and, when delivered intraperitoneally, in vivo, inhibiting tumor growth when given with doxorubicin . PGP-4008 also enhances the ability of docetaxel to inhibit growth and drive apoptosis in ovarian cancer cells.
[Uses]

PGP-4008 is a specific P-glycoprotein (Pgp) inhibitor. PGP-4008 inhibits tumor growth in a murine syngeneic Pgp-mediated multiple agent resistance (MDR) solid tumor model when given in combination with Doxorubicin[1].
[storage]

Store at -20°C
[References]

[1] Brian D Lee, et al. Synthesis and evaluation of dihydropyrroloquinolines that selectively antagonize P-glycoprotein. J Med Chem. 2004 Mar 11;47(6):1413-22. DOI:10.1021/jm0303204
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