Description:
SU 4312 is a potent and selective inhibitor of VEGFR and PDGFR tyrosine kinases (IC50 = 0.8 and 19.4 μM, respectively) wirth selectivity over EGFR and c-Src tyrosine kinases.
- Molecular Weight:264.33
- Boiling Point:497.1±45.0°C at 760 mmHg
- Melting Point:225-232°C
- Purity:≥95%
Molecular Formula:
C17H16N2O
Canonical SMILES:
CN(C)C1=CC=C(C=C1)C=C2C3=CC=CC=C3NC2=O
InChI:
InChI=1S/C17H16N2O/c1-19(2)13-9-7-12(8-10-13)11-15-14-5-3-4-6-16(14)18-17(15)20/h3-11H,1-2H3,(H,18,20)
InChIKey:
UAKWLVYMKBWHMX-UHFFFAOYSA-N
Solubility:
Soluble in DMSO
Storage: Store at -20°C
Synonyms:
SU4312; SU-4312; 3-[[4-(dimethylamino)phenyl]methylene]-1,3-dihydro-2H-indol-2-one; 2H-Indol-2-one, 3-[[4-(dimethylamino)phenyl]methylene]-1,3-dihydro-; 2-Indolinone, 3-[p-(dimethylamino)benzylidene]-; 3-(4-Dimethylaminobenzylidenyl)-2-indolinone; 3-[[4-(Dimethylamino)phenyl]methylidene]-2,3-dihydro-1H-indol-2-one; DMBI; NSC 86429 Weitere Informationen finden Sie
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