Structure of BIX-01294
CAS No.: 935693-62-2
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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.
BIX-01294 is a reversible and highly selective G9a and GLP histone methyltransferase inhibitor with IC50 values of 1.7 μM and 0.9 μM, respectively. BIX-01294 competes for binding with amino acids N-terminal of the substrate lysine residue, inducing necroptosis and autophagy, and has antitumor activity in recurrent tumor cells.
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CAS No. : | 935693-62-2 |
Formula : | C28H38N6O2 |
M.W : | 490.64 |
SMILES Code : | CN1CCN(C2=NC(NC3CCN(CC4=CC=CC=C4)CC3)=C5C=C(OC)C(OC)=CC5=N2)CCC1 |
MDL No. : | MFCD14560563 |
InChI Key : | OSXFATOLZGZLSK-UHFFFAOYSA-N |
Pubchem ID : | 25150857 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
Bladder cancer cell line J82 | 2–5 μM | 1-6 days | Significantly reduced the global levels of H3K9me1 and H3K9me2 and completely inhibited the proliferation of all the cancer cell lines examined | PMC3878056 |
Bone cancer cell line U2OS | 2–5 μM | 1-6 days | Significantly reduced the global levels of H3K9me1 and H3K9me2 and completely inhibited the proliferation of all the cancer cell lines examined | PMC3878056 |
Brain cancer cell line U251 | 2–5 μM | 1-6 days | Significantly reduced the global levels of H3K9me1 and H3K9me2 and completely inhibited the proliferation of all the cancer cell lines examined | PMC3878056 |
Breast cancer cell lines MCF10A and MCF7 | 2–5 μM | 1-6 days | Significantly reduced the global levels of H3K9me1 and H3K9me2 and completely inhibited the proliferation of all the cancer cell lines examined | PMC3878056 |
Cervical cancer cell line HeLa | 2–5 μM | 1-6 days | Significantly reduced the global levels of H3K9me1 and H3K9me2 and completely inhibited the proliferation of all the cancer cell lines examined | PMC3878056 |
Colon cancer cell lines HCT116 and RKO | 2–5 μM | 1-6 days | Significantly reduced the global levels of H3K9me1 and H3K9me2 and completely inhibited the proliferation of all the cancer cell lines examined | PMC3878056 |
Liver cancer cell line Hep2G | 2–5 μM | 1-6 days | Significantly reduced the global levels of H3K9me1 and H3K9me2 and completely inhibited the proliferation of all the cancer cell lines examined | PMC3878056 |
Lung cancer cell line H1299 | 2–5 μM | 1-6 days | Significantly reduced the global levels of H3K9me1 and H3K9me2 and completely inhibited the proliferation of all the cancer cell lines examined | PMC3878056 |
Sympathetic nervous system cancer cell lines BE(2)-C, SMS-KCNR, and SHEP1 | 2–5 μM | 1-6 days | Significantly reduced the global levels of H3K9me1 and H3K9me2 and completely inhibited the proliferation of all the cancer cell lines examined | PMC3878056 |
DPSCs | 1 μM | 2 weeks | BIX-01294 significantly promotes the chondrogenic differentiation of DPSCs, as indicated by the augmented expression levels of cartilage-signature markers and markedly increased proteoglycans. | PMC10460901 |
HCT116 cells | 5 µM | 24 hours | To examine the effect of BIX-01294 on FOXO1 methylation, results showed decreased FOXO1 methylation levels | PMC6393239 |
DLD-1 cells | 5 µM | 24 hours | To examine the effect of BIX-01294 on FOXO1 methylation, results showed decreased FOXO1 methylation levels | PMC6393239 |
SW480 cells | 5 µM | 24 hours | To examine the effect of BIX-01294 on FOXO1 methylation, results showed decreased FOXO1 methylation levels | PMC6393239 |
HEY cells | 5 μM | 24 hours | BIX-01294 significantly up-regulated the transcriptional expression of SLC31A1 and reduced the IC50 value of CDDP, increasing CDDP sensitivity. | PMC8441092 |
SKOV3 cells | 5 μM | 24 hours | BIX-01294 significantly up-regulated the transcriptional expression of SLC31A1 and reduced the IC50 value of CDDP, increasing CDDP sensitivity. | PMC8441092 |
JEG-3 placental choriocarcinoma cells | 3.3 µM | 3 days | BIX-01294 showed an IC50 value of 3.3 μM in JEG-3 cells, demonstrating selectivity for the parasite. | PMC3478629 |
Human foreskin fibroblasts (HFF) | 6.1 µM | 3 days | BIX-01294 showed an IC50 value of 6.1 μM in HFF cells, demonstrating selectivity for the parasite. | PMC3478629 |
Mouse embryonic fibroblasts (MEF) | 11 µM | 3 days | BIX-01294 showed an IC50 value of 11 μM in MEF cells, demonstrating selectivity for the parasite. | PMC3478629 |
Plasmodium falciparum 3D7 | 100 nM | 3 hours | BIX-01294 and TM2-115 inhibited P. falciparum 3D7 parasites in culture with IC50 values of ~100 nM, and significantly reduced parasite viability within 3 hours. | PMC3478629 |
KG1 cells | 10 μM | 48 hours | BIX-01294 activated the PERK/NRF2 pathway and upregulated HO-1 expression, suppressing p38 phosphorylation and intracellular ROS generation, thereby inhibiting apoptosis in KG1 cells. | PMC7158163 |
U937 cells | 10 μM | 48 hours | BIX-01294 markedly induced p38 phosphorylation and apoptosis in U937 cells. | PMC7158163 |
EGFR-mutant NSCLC cells (PC9 and H1975) | 10 µM | 48 hours | BIX significantly induced apoptosis and activated effector caspase-3 and PARP. | PMC8741967 |
EGFR-WT NSCLC cells (H460 and A549) | 10 µM | 48 hours | BIX had no significant apoptotic effect on EGFR-WT cells. | PMC8741967 |
K-ras NIH 3T3 transformed cells | 2.5 µM | 72 hours | BIX-01294 treatment reversed Ras-mediated epigenetic silencing of the Fas gene, similar to the effect of 5-aza treatment. | PMC2676930 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
severe combined immunodeficiency mice | EGFR-mutant NSCLC xenograft model | intraperitoneally | 5 mg/kg or 10 mg/kg | 2 days a week for 4 weeks | BIX significantly inhibited the growth of EGFR-mutant tumors and reduced EGFR expression. | PMC8741967 |
Nude mice | intra-peritoneal tumor model | intra-peritoneal injection | 5 mg/kg | twice a week for six weeks | BIX-01294 significantly reduced tumor growth and prolonged the survival time of tumor-bearing mice, increasing CDDP sensitivity. | PMC8441092 |
Mice | Plasmodium berghei ANKA infection model | Intraperitoneal injection | 40 mg/kg | Single dose | A single intraperitoneal dose of 40 mg/kg BIX-01294 reduced parasitemia by 2-fold in mice, and the mice survived for more than 3 weeks post-infection. | PMC3478629 |
Bio Calculators | ||||
Preparing Stock Solutions | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.04mL 0.41mL 0.20mL |
10.19mL 2.04mL 1.02mL |
20.38mL 4.08mL 2.04mL |
Tags: BIX-01294 | BIX01294 | BIX 01294 | Histone Methyltransferase | Autophagy | H3K9me2 | H3K9me3 | G9a inhibitor | GLP inhibitor | histone methyltransferase | necroptosis | p53 | Cdkn1a | p21 | Gadd45a | SUV39H1(H320R) | PRMT1 | 935693-62-2
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