NVP-BVU 972

NVP-BVU 972 Basic information
Product Name:NVP-BVU 972
Synonyms:6-[[6-(1-Methyl-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-3-yl]methyl]quinoline NVP-BVU972;NVP-BVU 972;NVP-BVU972;6-[[6-(1-Methyl-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-3-yl]methyl]quinoline;NVP-BVU972, >=98%;NVP-BVU972;NVP-BVU 972;CS-529;Quinoline, 6-[[6-(1-methyl-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-3-yl]methyl]-
CAS:1185763-69-2
MF:C20H16N6
MW:340.38
EINECS:200-258-5
Product Categories:Inhibitors
Mol File:1185763-69-2.mol
NVP-BVU 972 Structure
NVP-BVU 972 Chemical Properties
density 1.35
storage temp. Store at -20°C
solubility insoluble in H2O; ≥17 mg/mL in DMSO; ≥25.15 mg/mL in EtOH
form solid
pka4.92±0.10(Predicted)
Safety Information
MSDS Information
NVP-BVU 972 Usage And Synthesis
UsesNVP-BVU972 exhibits strong inhibition towards MET kinase but displays low inhibition against other kinases including the most closely related kinase RON.
Biological Activitynvp-bvu972 is a selective and potent inhibitor of c-met with ic50 of 14 nm. besides, nvp-bvu972 displays ic50 values more than 1000 nm in other kinases such as the most closely related kinase recepteur d'origine nantais (ron).c-met, also known as hepatocyte growth factor receptor, is a receptor tyrosine kinase that can be activated by hepatocyte growth factor/scatter factor (hgf/sf). it is a membrane protein which plays an essential role in embryonic development and wound healing.in the ebc-1, gtl-16, and mkn-45 human cancer cells, nvp-bvu972 potently inhibits the cell proliferation with ic50 values of 82, 66 and 32 nm, respectively. additionally, nvp-bvu972 treatment leads to the inhibition of the growth of the transformed mouse baf3 cells containing tpr-met kinase fusions with ic50 of 104 nm 1.in human sample, nvp-bvu972 treatment on cells expressing wild-type tpr-met resulted in a dose-dependent reduction in tpr-met phosphorylation. y1230h, d1228a, f1200i and l1195v mutations abrogate the tpr-met phosphorylation inhibition effect of nvp-bvu972 in baf3 tpr-met1.
targetMet
references1. tiedt r, degenkolbe e, furet p, et al. a drug resistance screen using a selective met inhibitor reveals a spectrum of mutations that partially overlap with activating mutations found in cancer patients. cancer research. 2011;71(15):5255-5264.
NVP-BVU 972 Preparation Products And Raw materials
1,2-Dihydro-5-methyl-2-phenyl-3H-pyrazol-3-one BMS-794833 Dovitinib 6-Amino-N-[3-[4-(4-morpholinyl)pyrido[3',2':4,5]furo[3,2-d]pyrimidin-2-yl]phenyl]-3-pyridinecarboxamide Luminespib 5-Hydroxy-1-methylpyrazole 6-[2-tert-Butyl-5-(6-methyl-pyridin-2-yl)-1H-imidazol-4-yl]-quinoxaline Nutlin 3a TAE226 (NVP-TAE226) R428 Tozasertib GDC-0068 2-[[(1R)-1-[7-methyl-2-(4-morpholinyl)-4-oxo-4h-pyrido[1,2-a]pyrimidin-9-yl]ethyl]amino]benzoic acid MLN0905 BKM120 (NVP-BKM120, Buparlisib) ARRY-424704, ARRY-704 Binimetinib 1-Methylpyrazole

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