| Identification | Back Directory | [Name]
J22352 | [CAS]
2252395-44-9 | [Synonyms]
J22352
Benzamide, 4-[[3,4-dihydro-2,4-dioxo-3-(2-phenylethyl)-1(2H)-quinazolinyl]methyl]-N-hydroxy- | [Molecular Formula]
C24H21N3O4 | [MDL Number]
MFCD32062835 | [MOL File]
2252395-44-9.mol | [Molecular Weight]
415.44 |
| Chemical Properties | Back Directory | [density ]
1.343±0.06 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
DMSO:125.0(Max Conc. mg/mL);300.88(Max Conc. mM) | [form ]
Solid | [pka]
8.91±0.10(Predicted) | [color ]
Light yellow to yellow |
| Hazard Information | Back Directory | [Description]
J22352 is a PROTAC (proteolysis-targeting chimeras)-like and highly selective HDAC6 inhibitor. J22352 promotes HDAC6 degradation and induces anticancer effects by inhibiting autophagy and eliciting the antitumor immune response in glioblastoma cancers, and leading to the restoration of host antitumor activity by reducing the immunosuppressive activity of PD-L1. | [Uses]
J22352 is a PROTAC (proteolysis-targeting chimeras)-like and highly selective HDAC6 inhibitor with an IC50 value of 4.7 nM. J22352 promotes HDAC6 degradation and induces anticancer effects by inhibiting autophagy and eliciting the antitumor immune response in glioblastoma cancers, and leading to the restoration of host antitumor activity by reducing the immunosuppressive activity of PD-L1[1]. | [in vitro]
The consequences of decreased HDAC6 expression in response to J22352 decreased cell migration, increased autophagic cancer cell death and significant tumor growth inhibition. Notably, J22352 reduced the immunosuppressive activity of PD-L1, leading to the restoration of host anti-tumor activity. These results demonstrate that J22352 promotes HDAC6 degradation and induces anticancer effects by inhibiting autophagy and eliciting the antitumor immune response in glioblastoma._x000D_
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Reference: Biochem Pharmacol. 2019 May;163:458-471. https://pubmed.ncbi.nlm.nih.gov/30885763/ | [in vivo]
The consequences of decreased HDAC6 expression in response to J22352 decreased cell migration, increased autophagic cancer cell death and significant tumor growth inhibition. Notably, J22352 reduced the immunosuppressive activity of PD-L1, leading to the restoration of host anti-tumor activity. These results demonstrate that J22352 promotes HDAC6 degradation and induces anticancer effects by inhibiting autophagy and eliciting the antitumor immune response in glioblastoma._x000D_
_x000D_
Reference: Biochem Pharmacol. 2019 May;163:458-471. https://pubmed.ncbi.nlm.nih.gov/30885763/ | [target]
J22352 is a PROTAC (proteolysis-targeting chimeras)-like and highly selective HDAC6 inhibitor with an IC50 value of 4.7 nM. | [IC 50]
HDAC6: 4.7 nM (IC50) | [References]
[1] Liu JR, et al. High-selective HDAC6 inhibitor promotes HDAC6 degradation following autophagy modulation and enhanced antitumor immunity in glioblastoma. Biochem Pharmacol. 2019 May; 163:458-471. DOI:10.1016/j.bcp.2019.03.023 |
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| Company Name: |
cjbscvictory
|
| Tel: |
13348960310 |
| Website: |
https://www.weikeqi-biotech.com/ |
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