2,4-Thiazolidinedione, 3-[[(3Z)-2,3-dihydro-3-[[4-(4-MorpholinylMethyl)-1H-pyrrol-2- yl]Methylene]-2-oxo-1H-indol-5-yl]Methyl]-, hydrochloride

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2,4-Thiazolidinedione, 3-[[(3Z)-2,3-dihydro-3-[[4-(4-MorpholinylMethyl)-1H-pyrrol-2- yl]Methylene]-2-oxo-1H-indol-5-yl]Methyl]-, hydrochloride Suppliers list
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2,4-Thiazolidinedione, 3-[[(3Z)-2,3-dihydro-3-[[4-(4-MorpholinylMethyl)-1H-pyrrol-2- yl]Methylene]-2-oxo-1H-indol-5-yl]Methyl]-, hydrochloride Basic information
Product Name:2,4-Thiazolidinedione, 3-[[(3Z)-2,3-dihydro-3-[[4-(4-MorpholinylMethyl)-1H-pyrrol-2- yl]Methylene]-2-oxo-1H-indol-5-yl]Methyl]-, hydrochloride
Synonyms:2,4-Thiazolidinedione, 3-[[(3Z)-2,3-dihydro-3-[[4-(4-MorpholinylMethyl)-1H-pyrrol-2- yl]Methylene]-2-oxo-1H-indol-5-yl]Methyl]-, hydrochloride;(Z)-3-((3-((4-(morpholinomethyl)-1H-pyrrol-2-yl)methylene)-2-oxoindolin-5-yl)methyl)thiazolidine-2,4-dione hydrochloride;2,4-Thiazolidinedione, 3-[[(3Z)-2,3-dihydro-3-[[4-(4-morpholinylmethyl)-1H-pyrrol-2-yl]methyle;112180
CAS:1265965-19-2
MF:C22H23ClN4O4S
MW:474.96042
EINECS:
Product Categories:
Mol File:1265965-19-2.mol
2,4-Thiazolidinedione, 3-[[(3Z)-2,3-dihydro-3-[[4-(4-MorpholinylMethyl)-1H-pyrrol-2- yl]Methylene]-2-oxo-1H-indol-5-yl]Methyl]-, hydrochloride Structure
2,4-Thiazolidinedione, 3-[[(3Z)-2,3-dihydro-3-[[4-(4-MorpholinylMethyl)-1H-pyrrol-2- yl]Methylene]-2-oxo-1H-indol-5-yl]Methyl]-, hydrochloride Chemical Properties
storage temp. Store at 0-8 °C
solubility DMSO: Sparingly Soluble: 1-10 mg/ml
Safety Information
MSDS Information
2,4-Thiazolidinedione, 3-[[(3Z)-2,3-dihydro-3-[[4-(4-MorpholinylMethyl)-1H-pyrrol-2- yl]Methylene]-2-oxo-1H-indol-5-yl]Methyl]-, hydrochloride Usage And Synthesis
Uses(Z)-S49076 hydrochloride is an orally active inhibitor of MET and AXL that blocks the downstream signaling of these receptors both in vitro and in vivo, inhibiting the proliferation and migration of tumor cells and suppressing tumor growth in xenograft models. (Z)-S49076 hydrochloride is capable of overcoming the resistance to epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) due to MET amplification in Erlotinib (HY-50896)-resistant cell lines both in vitro and in vivo. (Z)-S49076 hydrochloride can be used for research in non-small cell lung cancer (NSCLC)[1].
References[1] Park K, et al. Phase I results of S49076 plus gefitinib in patients with EGFR TKI-resistant non-small cell lung cancer harbouring MET/AXL dysregulation[J]. Lung Cancer, 2021, 155: 127-135. DOI:10.1016/j.lungcan.2021.03.012
[2] MIKE F BURBRIDGE. S49076 is a novel kinase inhibitor of MET, AXL, and FGFR with strong preclinical activity alone and in association with bevacizumab.[J]. Molecular Cancer Therapeutics, 2013, 12 9: 1749-1762. DOI: 10.1158/1535-7163.mct-13-0075
2,4-Thiazolidinedione, 3-[[(3Z)-2,3-dihydro-3-[[4-(4-MorpholinylMethyl)-1H-pyrrol-2- yl]Methylene]-2-oxo-1H-indol-5-yl]Methyl]-, hydrochloride Preparation Products And Raw materials
Tag:2,4-Thiazolidinedione, 3-[[(3Z)-2,3-dihydro-3-[[4-(4-MorpholinylMethyl)-1H-pyrrol-2- yl]Methylene]-2-oxo-1H-indol-5-yl]Methyl]-, hydrochloride(1265965-19-2) Related Product Information
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