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p110a PI3K inhibitor selective for p110 isoform activated in HER2+ breast cancers and gastric cancers. It inhibits proliferation of breast cancer cells and decreases invasiveness of squamous cell lung cancer cells. (C08-0488-459)

Thomas Scientific

Catalog No.
C08-0488-459
Manufacturer No.
B9700-1 mg
Manufacturer Name
LKT Laboratories, Inc
Quantity
1
Unit of Measure
EA
Price: $126.53
List Price: $140.59

BYL-719 is an ATP-competitive oral PI3K inhibitor selective for the p110a isoform that is activated by a mutant PIK3CA gene in HER2+ breast cancers and gastric cancers. BYL-719 exhibits anticancer chemotherapeutic activity and inhibits proliferation

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BYL-719 is an ATP-competitive oral PI3K inhibitor selective for the p110a isoform that is activated by a mutant PIK3CA gene in HER2+ breast cancers and gastric cancers. BYL-719 exhibits anticancer chemotherapeutic activity and inhibits proliferation in a variety of cell lines. IGF1 and neuregulin 1 activate mTOR, a downstream target of PI3K that mediates resistance to BYL-719 in some in vitro cancer models. This compound also decreases invasion and epithelial-to-mesenchymal transition (EMT) in cellular and animal models of squamous cell lung cancer. Grades: ≥99%, ≥99%ee
UPC:
41122409
Condition:
New
Availability:
3 Days
Weight:
1.00 Ounces
HazmatClass:
No
WeightUOM:
LB
MPN:
B9700-1 mg
CAS:
1217486-61-7


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