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BGC > Product Search > SU 4312 | 5812-07-7
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Suppliers for

SU 4312



Properties

CAS   5812-07-7 
Formula   C17H16N2

Structure

6 Registered suppliers


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

More details are to be found here
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

More details are to be found here
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

More details are to be found here

Detailed information on the suppliers of SU 4312

Properties:

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