Name | SU 4312 |
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Synonyms |
3-[[4-(dimethylamino)phenyl]methylene]-1,3-dihydro-2H-indol-2-one
NSC 86429 |
Description | SU4312 is the racemate of (Z)-SU4312 and (E)-SU4312. (Z)-SU4312 inhibits PDGFR and FLK-1 with IC50s of 19.4 and 0.8 μM, respectively. (E)-SU4312 inhibits PDGFR, FLK-1, EGFR, HER-2, and IGF-1R with IC50s of 24.2, 5.2, 18.5, 16.9 and 10.0 μM, respectively[1]. |
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Related Catalog | |
Target |
PDGFR Flk-1 |
In Vitro | Receptor tyrosine kinases (RTKs) have been shown to be important mediators of cellular signal transduction in cells. Many RTKs have been shown to be oncogene products implicating their role in the transformation process associated with human cancers[1]. |
References |
Density | 1.219g/cm3 |
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Boiling Point | 497.1ºC at 760 mmHg |
Molecular Formula | C17H16N2O |
Molecular Weight | 264.32200 |
Flash Point | 254.5ºC |
Exact Mass | 264.12600 |
PSA | 32.34000 |
LogP | 3.38330 |
Index of Refraction | 1.683 |
Storage condition | -20℃ |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
RIDADR | NONH for all modes of transport |