Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C25H30N6O5 |
Molecular Weight | 494.5429 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(OC[C@H](O)CN2CCOCC2)C=CC3=C1N=C(NC(=O)C4=CC=CN=C4C)N5CCN=C35
InChI
InChIKey=JGNRMIWLBBNSMU-QGZVFWFLSA-N
InChI=1S/C25H30N6O5/c1-16-18(4-3-7-26-16)24(33)29-25-28-21-19(23-27-8-9-31(23)25)5-6-20(22(21)34-2)36-15-17(32)14-30-10-12-35-13-11-30/h3-7,17,32H,8-15H2,1-2H3,(H,28,29,33)/t17-/m1/s1
Molecular Formula | C25H30N6O5 |
Molecular Weight | 494.5429 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionCurator's Comment: The description was created based on several sources, including
https://encrypted.google.com/patents/WO2015082376A3 | https://www.google.com/patents/WO2012062748A1
Curator's Comment: The description was created based on several sources, including
https://encrypted.google.com/patents/WO2015082376A3 | https://www.google.com/patents/WO2012062748A1
BAY-1082439 is an orally bioavailable inhibitor of the class I phosphoinositide 3-kinase (PI3K) alpha and beta isoforms with potential antineoplastic activity. PI3K alpha/beta inhibitor BAY1082439 selectively inhibits both PI3K alpha, including mutated forms of PIK3CA, and PI3K beta in the PI3K/Akt/mTOR pathway, which may result in tumor cell apoptosis and growth inhibition in PI3K-expressing and/or PTEN-driven tumor cells. By specifically targeting class I PI3K alpha and beta, this agent may be more efficacious and less toxic than pan PI3K inhibitors. Dysregulation of the PI3K/Akt/mTOR pathway is frequently found in solid tumors and results in increased tumor cell growth, survival, and resistance to chemotherapy and radiotherapy. PIK3CA, one of the most highly mutated oncogenes, encodes the p110-alpha catalytic subunit of the class I PI3K. PTEN, a tumor suppressor protein and negative regulator of PI3K activity, is often mutated in a variety of cancer cells.
Originator
Sources: https://www.google.com/patents/WO2012062748A1
Curator's Comment: # Bayer Pharma Aktiengesellschaft
Approval Year
Sample Use Guides
In Vitro Use Guide
Sources: https://encrypted.google.com/patents/WO2015082376A3
The effects of PI3K inhibitor Compound A1 (BAY-1082439) in MCF-7 and 4T1 breast cancer cells and PC-3 and LNCaP prostate cancer cells were investigated in vitro. The effects were studied by measuring cell proliferation and apoptosis. The PI3K inhibitor(BAY-1082439) was added at day -1 and at day 4 at 250 nM and 500 nM
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 19:07:36 GMT 2023
by
admin
on
Sat Dec 16 19:07:36 GMT 2023
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Record UNII |
59784ZX4GD
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Record Status |
Validated (UNII)
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Record Version |
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C103861
Created by
admin on Sat Dec 16 19:07:37 GMT 2023 , Edited by admin on Sat Dec 16 19:07:37 GMT 2023
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