CAS 1207293-36-4

BI-847325

CAS: 1207293-36-4

Formel: C₂₉H₂₈N₄O₂

Reinheit: 98%

Farbe und Form: Solid

Molekulargewicht: 464.5582

Ref: IN-DA008ZUA

BI-847325

CAS: 1207293-36-4

BI-847325

Formel: C₂₉H₂₈N₄O₂

Reinheit: ≥95%

Molekulargewicht: 464.56

Ref: 54-BUP02662

3-(3-(((4-((Dimethylamino)Methyl)Phenyl)Amino)(Phenyl)Methylene)-2-Oxoindolin-6-Yl)-N-Ethylpropiolamide

CAS: 1207293-36-4

3-(3-(((4-((Dimethylamino)Methyl)Phenyl)Amino)(Phenyl)Methylene)-2-Oxoindolin-6-Yl)-N-Ethylpropiolamide

Formel: C₂₉H₂₈N₄O₂

Reinheit: 99+%

Molekulargewicht: 464.56

Ref: 54-OR1024038

BI-847325

CAS: 1207293-36-4

BI-847325 is a selective dual inhibitor of MEK and aurora kinases (AK) with IC50 values of 4 and 15 nM for human MEK2 and AK-C, respectively.

Formel: C₂₉H₂₈N₄O₂

Reinheit: 97.13% - 97.54%

Farbe und Form: Yellow Solid

Molekulargewicht: 464.56

Ref: TM-T6785

BI-847325

CAS: 1207293-36-4

3-(3-(((4-((Dimethylamino)methyl)phenyl)amino)(phenyl)methylene)-2-oxoindolin-6-yl)-N-ethylpropiolamide

Formel: C₂₉H₂₈N₄O₂

Reinheit: 99+%

Molekulargewicht: 464.56

Ref: IN-DG328372

BI-847325

CAS: 1207293-36-4

BI-847325 is a new compound that inhibits the expression of genes that are involved in the development of cancer. It has been shown to have a potent inhibitory effect on cell proliferation and pro-apoptotic protein. BI-847325 is orally active, crossing the blood brain barrier in animals, and has a low toxicity profile. BI-847325 inhibits RNA synthesis by binding to the enzyme rRNA polymerase or by inhibiting ribosome activity. This compound also inhibits ATP levels and replication of DNA in liver cells, which may be due to its ability to bind to metagene sequences. BI-847325 has demonstrated promising results in animal studies for gastrointestinal toxicities, with no evidence of weight loss or anorexia at doses up to 15 times higher than the dose required for efficacy against cancer cells.

Formel: C₂₉H₂₈N₄O₂

Reinheit: Min. 95%

Molekulargewicht: 464.56 g/mol

Ref: 3D-HYB29336