| Identification | Back Directory | [Name]
4-[6-iodo-2-[(E)-2-(3-methylphenyl)ethenyl]-4-oxoquinazolin-3-yl]benzoic acid | [CAS]
500273-31-4 | [Synonyms]
4-[6-iodo-2-[(E)-2-(3-methylphenyl)ethenyl]-4-oxoquinazolin-3-yl]benzoic acid
Benzoic acid, 4-[6-iodo-2-[2-(3-methylphenyl)ethenyl]-4-oxo-3(4H)-quinazolinyl]- | [Molecular Formula]
C24H17IN2O3 | [MOL File]
500273-31-4.mol | [Molecular Weight]
508.31 |
| Chemical Properties | Back Directory | [Boiling point ]
680.2±65.0 °C(Predicted) | [density ]
1.54±0.1 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
DMSO: 2mg/mL, clear (Warmed) | [form ]
powder | [pka]
4.27±0.10(Predicted) | [color ]
white to beige |
| Hazard Information | Back Directory | [Uses]
BDM19 binds and activates cytosolic BAX dimers, and prompts cell apoptosis either alone or in combination with BCL-2/BCL-XL inhibitor Navitoclax (HY-10087)[1]. | [Biological Activity]
Potent and selective cytosolic BAX dimer modulator th at effectively induces apoptosis in cancer cells by selectively modulating inactive BAX.
BDM19a potent BAX dimer modulator with a Kd of 560 nMselectively binds to the N-terminal trigger site of inactive BAX thereby inhibiting its dimerization with an IC50 of 5 μM. By stabilizing the inactive conformation of BAXBDM-19 allosterically activates ittargeting cells containing cytosolic inactive BAX monomers and dimers. This leads to a dose-dependent translocation of BAX to mitochondriasubsequent cytochrome c releaseand induction of apoptosis. | [References]
[1] Gitego N, et al. Chemical modulation of cytosolic BAX homodimer potentiates BAX activation and apoptosis. Nat Commun. 2023;14(1):8381. Published 2023 Dec 16. DOI:10.1038/s41467-023-44084-3 |
|
| Company Name: |
Merck KGaA
|
| Tel: |
21-20338288 |
| Website: |
www.sigmaaldrich.cn |
| Company Name: |
PHARMEKS Ltd.
|
| Tel: |
+7 (495) 702-9648 |
| Website: |
www.pharmeks.com |
|