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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
Structure of BAY-1082439

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

HIDE SMILES / InChI

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

Description
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

Curator's Comment: # Bayer Pharma Aktiengesellschaft

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Patents

Patents

Sample Use Guides

15mg orally once daily with a 21 days cycle.
Route of Administration: Oral
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 Sat Dec 16 19:07:36 UTC 2023
Edited
by admin
on Sat Dec 16 19:07:36 UTC 2023
Record UNII
59784ZX4GD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BAY-1082439
Code English
BAY-1082439 [WHO-SDG]
Code English
3-PYRIDINECARBOXAMIDE, N-(2,3-DIHYDRO-8-((2R)-2-HYDROXY-3-(4-MORPHOLINYL)PROPOXY)-7-METHOXYIMIDAZO(1,2-C)QUINAZOLIN-5-YL)-2-METHYL-
Systematic Name English
N-(8-(((2R)-2-HYDROXY-3-(MORPHOLIN-4-YL)PROPYL)OXY)-7-METHOXY-2,3-DIHYDROIMIDAZO(1,2-C)QUINAZOLIN-5-YL)-2-METHYLPYRIDINE-3-CARBOXAMIDE
Systematic Name English
BAY1082439
Code English
BAY 1082439 [WHO-DD]
Common Name English
Code System Code Type Description
FDA UNII
59784ZX4GD
Created by admin on Sat Dec 16 19:07:37 UTC 2023 , Edited by admin on Sat Dec 16 19:07:37 UTC 2023
PRIMARY
CAS
1375469-38-7
Created by admin on Sat Dec 16 19:07:37 UTC 2023 , Edited by admin on Sat Dec 16 19:07:37 UTC 2023
PRIMARY
NCI_THESAURUS
C103861
Created by admin on Sat Dec 16 19:07:37 UTC 2023 , Edited by admin on Sat Dec 16 19:07:37 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY