Home Categories Biochemical Engineering R428 (BGB324)
A7131212

R428 (BGB324) , 98% , 1037624-75-1

CAS NO.:1037624-75-1

Empirical Formula: C30H34N8

Molecular Weight: 506.64

MDL number: MFCD28142765

Pack Size Price Stock Quantity
1MG RMB367.20 In Stock
5MG RMB927.20 In Stock
10MG RMB1599.20 In Stock
25MG RMB2154.40 In Stock
50mg RMB3391.20 In Stock
100mg RMB6103.20 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: >211°C (dec.)
Boiling point: 799.6±70.0 °C(Predicted)
Density  1.41±0.1 g/cm3(Predicted)
storage temp.  -20°C
solubility  Soluble in DMSO (up to at least 25 mg/ml)
pka 10.34±0.20(Predicted)
form  Yellow powder.
color  Yellow
Stability: Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
InChIKey KXMZDGSRSGHMMK-VWLOTQADSA-N
SMILES N1(C2=NN=C3C4=CC=CC=C4CCCC3=C2)C(N)=NC(NC2=CC=C3CC[C@H](N4CCCC4)CCC3=C2)=N1

Description and Uses

R428 (bemcentinib, BGB324), a selective small-molecule inhibitor of AXL, is currently being evaluated in phase II trials for the treatment of non-small-cell lung cancer (NSCLC) and acute myelocytic leukemia (AML). It has been found to induce apoptosis in cancer cells and to block tumor spread in models of metastatic breast cancer. The therapeutic potential of R428 has also been demonstrated in highly invasive esophageal adenocarcinoma cells and in ESCC cells.
R428 is a selective, small molecule inhibitor of Axl that blocks its catalytic and precancerous activities. R428 treatment reduced Axl-induced AKT phosphorylation, cancer cell invasion, angiogenesis, and the production of pro-inflammatory cytokines. It also reduced the expression of the cytokine granulocyte macrophage colony-stimulating factor and Snail in a dosage-dependent manner. Interestingly,using R428 to inhibit Axl-mediated cellular and molecular functions during cisplatin treatments achieved an enhanced suppression of liver metastases. Axl knockdowns in RAC cell lines reduced migration, invasion, and in vivo engraftment, accompanied by a downregulation in the activity of the Ral GTPase proteins (RalA and RalB). Similar effects were obtained using an A428 inhibitor. Blocking Axl functions also abrogated the phosphorylation of ERBB2 (Her-2/neu) at the Tyr877 residue, which reveals the cross-functional effects of R428 on different receptor signaling axes.
Cabozantinib (XL184) and R428 (BGB324) Inhibit the Growth of Esophageal Squamous Cell Carcinoma (ESCC)

R 428 is an AXL tyrosine kinase inhibitor shown to be used as an anti-cancer agent.

Safety

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

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