Structure of GSK-J4 HCl
CAS No.: 1797983-09-5
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
GSK-J4 hydrochloride is a potent dual inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and UTX/KDM6A with IC50 values of 8.6 μM and 6.6 μM, respectively. It inhibits LPS-induced TNF-α production in human primary macrophages with an IC50 of 9 μM and is a cell-permeable proagent of GSK-J1.
Synonyms: GSK-J4 (hydrochloride); GSK-J4 hydrochloride
4.5
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CAS No. : | 1797983-09-5 |
Formula : | C24H28ClN5O2 |
M.W : | 453.96 |
SMILES Code : | O=C(OCC)CCNC1=NC(C2=NC=CC=C2)=NC(N3CCC4=CC=CC=C4CC3)=C1.[H]Cl |
Synonyms : |
GSK-J4 (hydrochloride); GSK-J4 hydrochloride
|
MDL No. : | MFCD26142638 |
InChI Key : | TYXWLTBYINKVNT-UHFFFAOYSA-N |
Pubchem ID : | 71729974 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
Target |
|
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
WT EpdSCs | 10 μM | 24 h | prevented H3K27me3 loss and differentiation | PMC7343604 |
SOX2+ EpdSCs | 10 μM | 24 h | prevented H3K27me3 loss and differentiation | PMC7343604 |
neuroblastoma cell lines | 1 μM | 72 h | To evaluate the sensitivity of neuroblastoma cells to GSK-J4, results showed that some cells were highly sensitive to GSK-J4, with significantly reduced cell viability. | PMC6200133 |
IMR5 cells | 1 μM | 72 h | To analyze the gene expression changes in IMR5 cells treated with GSK-J4 through RNA sequencing, results showed that more than 7000 genes were significantly altered. | PMC6200133 |
K562 cells | 5 μM | 24 h | Restored H3K27me3 levels | PMC10760961 |
K562 cells | 5 μM | 72 h | Inhibited cell proliferation | PMC10760961 |
OCI-AML5 cells | 5 μM | 24, 48, 72 h | Increased H3K27me3 levels and decreased GATA2 and MEIS1 expression | PMC10760961 |
ER-Hoxb8 cells | 5 µM | 3 days | GSK-J4 treatment significantly decreased S100a8 and S100a9 mRNA levels in WT ER-Hoxb8 cells, while the effects on C/EBPδ KO cells were negligible | PMC9122501 |
lung cancer cells | 1 µM | 5 days | GSK-J4 was more toxic in SMARCA4-defective lung cancer cells, with a five-fold lower EC50 than in MYCamp cells | PMC8280185 |
ovarian cancer cells | 1 µM | 5 days | GSK-J4 strongly suppressed cell viability and clonogenic capability in SMARCA4-defective ovarian cancer cells | PMC8280185 |
osteoprogenitors | 1 μM | 30 min | GSK-J4 blocked the activation of MKP-1 by dexamethasone and restored the protein levels of p-JNK, p-ERK, p-p38, and PCNA, indicating that GSK-J4 alleviates the inhibitory effect of dexamethasone on osteoprogenitor proliferation by inhibiting H3K27me3 demethylation. | PMC11604782 |
SF8628 K27M DIPG cells | 6 μM | 6, 24, 48, 72 h | GSK-J4 significantly reduced the expression of DNA DSB repair genes and DNA accessibility, inhibiting DNA DSB repair. | PMC6744979 |
DIPG-007 K27M DIPG cells | 6 μM | 6, 24, 48, 72 h | GSK-J4 significantly reduced the expression of DNA DSB repair genes and DNA accessibility, inhibiting DNA DSB repair. | PMC6744979 |
SF9427 H3 wild-type GBM cells | 6 μM | 72 h | GSK-J4 did not alter the expression of DNA DSB repair genes in H3 wild-type GBM cells. | PMC6744979 |
143B cells | 15 μM | 72 h | To evaluate the effect of GSK-J4 on 143B cells, the results showed that GSK-J4 treatment increased H3K27me3 levels and enhanced the sensitivity of cells to cisplatin. | PMC6335728 |
HOS cells | 15 μM | 72 h | To evaluate the effect of GSK-J4 on HOS cells, the results showed that GSK-J4 treatment increased H3K27me3 levels and enhanced the sensitivity of cells to cisplatin. | PMC6335728 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
mice | tumor model | intraperitoneal injection | 10 mg/kg | daily for five days | prevented tumor differentiation | PMC7343604 |
Mice | Nestin-GFP mice | Intraperitoneal injection | 100 mg/kg | Daily for 2 weeks | To investigate the effect of GSK-J4 on the number of Nestin-GFP positive cells, results showed that GSK-J4 significantly increased the number of Nestin-GFP positive cells. | PMC5670205 |
Mice | KRAS+/Trp53-null lung cancer model | Intraperitoneal injection | 100 mg/kg | Once daily for 10 days | GSK-J4 inhibits the growth of Ezh2-deficient tumors. | PMC9859827 |
mice | CHLA20 and IMR32 xenograft models | intraperitoneal injection | 100 mg/kg | 5 days/week, throughout the experiment | To evaluate the antitumor activity of GSK-J4 in vivo, results showed that GSK-J4 significantly inhibited tumor growth and induced tumor regression. | PMC6200133 |
mice | Asxl1Y588XTg leukemic mouse model | intraperitoneal injection | 50 mg/kg | 5 times per week for 5 weeks | Reduced leukemic cell engraftment and tumor burden | PMC10760961 |
mice | orthotopic lung and ovarian cancer models | intraperitoneal injection | 50 mg/kg | once daily for 4 weeks | GSK-J4 significantly prolonged the survival of mice with SMARCA4-defective lung and ovarian tumors and reduced tumor growth | PMC8280185 |
mice | PDE model | intraperitoneal injection | 100 mg/kg | daily from GD12 until labor | GSK-J4 treatment significantly restored the trabecular area and Osterix+ cell area in the metaphyseal bone of PDE young mice offspring, indicating that GSK-J4 alleviates the negative impact of PDE on osteoprogenitor proliferation and bone development by inhibiting H3K27me3 demethylation. | PMC11604782 |
Athymic mice | SF8628 K27M DIPG xenograft model | Intraperitoneal injection | 100 mg/kg | Once daily for 10 consecutive days | GSK-J4 monotherapy significantly inhibited tumor growth and extended survival, and the combination therapy with radiation outperformed monotherapy. | PMC6744979 |
nude mice | osteosarcoma xenograft model | intraperitoneal injection | 50 mg/kg | once daily until the end of the experiment | To evaluate the effect of GSK-J4 on the osteosarcoma xenograft model, the results showed that GSK-J4 combined with cisplatin significantly reduced the size and weight of tumors and enhanced tumor cell apoptosis. | PMC6335728 |
Tags: GSK-J4 | Histone Demethylase | Apoptosis | H3K27me3/me2 | H3K27 | Jumonji C domain-containing histone demethylase | JmjC-KDMs | KDM6A | KDM6B | chromatin remodeling | JMJD3 | UTX | demethylation | 1797983-09-5
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