A 419259 (trihydrochloride) Datasheet DC Chemicals
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Cat.No DC9628
Name A 419259 (trihydrochloride)

Chemical Properties

CAS 1435934-25-0
Formula C29H37CL3N6O
MW 592.002683401108
Storage 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Biological activity

Description CAS NO.:1435934-25-0
Product Name:7-[trans-4-(4-methyl-1-piperazinyl)cyclohexyl]-5-(4-phenoxyphenyl )-7h-pyrrolo[2,3-d]pyrimidin-4-amine Trihydrochloride
Synonyms:7-[trans-4-(4-Methyl-1-piperazinyl)cyclohexyl]-5-(4-phenoxyphenyl )-7H-pyrrolo[2,3-d]pyrimidin-4-amine trihydrochloride;A 419259 trihydrochloride;A-419259 trihydrochloride;RK 20449 trihydrochloride;RK-20449 trihydrochloride;A 419259 (trihydrochloride)
EINEC:
Molecular Formula:C29H37CL3N6O
Molecular Weight:592.002683401108
Target:
In Vivo
In Vitro A 419259 Trihydrochloride is a second-generation pyrrolo-pyrimidine designed to enhance selectivity towards the Src family relative to other cytoplasmic tyrosine kinases. A-419259 inhibits K-562 cells with an IC50 between 0.1 and 0.3 μM, and Meg-01 proliferation with an IC50 of approximately 0.1 μM. A-419259 also potently induces apoptosis in K-562 cells beginning at 0.1 μM and increasing in a dose-dependent manner. PP2 inhibits Src kinase autophosphorylation in both Ph+ cell lines (K-562 and Meg-01) with an IC50 between 3 and 10 μM, while A-419259 blocks kinase activation between 0.1 and 0.3 μM. A-419259 strongly inhibits DAGM/Bcr-Abl cell proliferation in the absence of IL-3 with an IC50 between 0.1 and 0.3 μM[1]. A-419259 is a broad-spectrum pyrrolo-pyrimidine inhibitor, and blocks proliferation and induces apoptosis in CML cell lines. A-419259 inhibits overall SFK activity in K562 and other CML cell lines with an IC50 value of 0.1-0.3 μM[2].
Kinase Assay
Cell Assay
Animal Administration

References

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