CAS 252916-29-3 | TSU-68 | Orantinib (SU6668)
Name: Orantinib (SU6668) CAS: 252916-29-3 MF: C18H18N2O3 MW: 310.35 Purity: 98% Package: 100g;1kg;10kg; Made in China Worldwide Delivery
Categories:
Other Material Chemicals
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Product introduction
Introduction and application of CAS 252916-29-3 Orantinib (SU6668)
Synonyms:
1H-Pyrrole-3-propanoic acid, 5-[(1,2-dihydro-2-oxo-3H-indol-3-ylidene)Methyl]-2,4-diMethyl-;
SU 6668(TSU-68);
(E)-3-(2,4-diMethyl-5-((2-oxoindolin-3-ylidene)Methyl)-1H-pyrrol-3-yl)propanoic acid;
3-[2,4-dimethyl-5-[(E)-(2-oxo-1H-indol-3-ylidene)methyl]-1H-pyrrol-3-yl]propanoic acid;
(Z)-3-(2,4-dimethyl-5-((2-oxoindolin-3-ylidene)methyl)-1H-pyrrol-3-yl)propanoic acid;
Specification:
|
ITEMS |
SPECIFICATION |
|
CAS |
252916-29-3 |
|
MF |
C18H18N2O3 |
|
MW |
310.35 |
|
Melting point |
252-254 °C |
|
Boiling point |
590.5±50.0 °C(Predicted) |
|
Density |
1.306±0.06 g/cm3(Predicted) |
|
Acidity coefficient |
4?+-.0.10(Predicted) |
|
Color |
Orange to brown |
|
Form |
Powder |
|
Storage condition |
Store at RT |
Use:
1.An orally bioavailable receptor tyrosine kinase inhibitor. Orantinib binds to and inhibits the autophosphorylation of vascular endothelial growth factor receptor 2 (VEGFR2), platelet-derived growth factor receptor (PDGFR), and fibroblast growth factor receptor (FGFR), thereby inhibiting angiogenesis and cell proliferation. Orantinib also inhibits the phosphorylation of the stem cell factor receptor tyrosine kinase c-kit, often expressed in acute myelogenous leukemia cells.
2.Orantinib (SU6668; TSU-68) is a multi-targeted receptor tyrosine kinase inhibitor with Ki values of 2.1 μM, 8 nM and 1.2 μM for Flt-1, PDGFRβ and FGFR1, respectively. Orantinib (TSU-68) has been shown to inhibit VEGFR2, PDGFRβ and FGFR1. Clinical studies have shown that orantinib has the activity of stabilizing disease progression after chemoembolization in advanced hepatocellular carcinoma.
production method: N/A
Package and transportation: Normal
Package: 100g;1kg;10kg;
Transportation: by courier/ by air/ by sea
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