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4551-00-2

4551-00-2 Structure

4551-00-2 Structure
IdentificationBack Directory
[Name]

9H-Fluorene,9-[3-(2-nitrophenyl)-2-propen-1-ylidene]-
[CAS]

4551-00-2
[Synonyms]

NSC-70220
SOS1 inhibitor 1
9H-Fluorene,9-[3-(2-nitrophenyl)-2-propen-1-ylidene]-
[Molecular Formula]

C22H15NO2
[MDL Number]

MFCD00032941
[MOL File]

4551-00-2.mol
[Molecular Weight]

325.36
Chemical PropertiesBack Directory
[Melting point ]

186 °C
[Boiling point ]

569.6±49.0 °C(Predicted)
[density ]

1.321±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C,unstable in solution, ready to use.
[solubility ]

DMSO: 12.5 mg/mL (38.42 mM)
[form ]

Solid
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Uses]

NSC-70220 is a selective and allosteric SOS1 inhibitor. NSC-70220 inhibits allosteric site activation, and partially inhibited catalytic site activation. NSC-70220 has an anticancer effect[1].
[Biological Activity]

NSC-70220 is a selective allosteric SOS1 inhibitor. It has an anticancer effects and inhibits allosteric site activation and partially inhibits catalytic site activation.
[in vitro]

The growth inhibitory rate (IR)=(average OD value in the control group-average OD value in the treatment group)/average OD value in the control group×100% are compared. Treatments with NSC-70220 at 40 μM and NSC-658497 at 30 μM result in growth inhibitory rate of 29% and 8% respectively. The combination treatment results in growth inhibitory rate of 54%, showing the synergistic effect of NSC-70220 and NSC-658497 on cell growth It is showed that the treatment with NSC-658497 at 40 μM for 2 hours alone or in combìnation with the treatment with 40 μM of NSC-70220 overnight resulted in lower expression levels of P-AKT and P-ERK. The treatment wlth 40 μM of NSC-70220 overnight resulted in lower expression levels of P-ERK.

[target]

SOS1.

[References]

[1] ARYL SULFONOHYDRAZIDES. WO 2016077793A1.
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