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ChemicalBook--->CAS DataBase List--->102586-30-1

102586-30-1

102586-30-1 Structure

102586-30-1 Structure
IdentificationBack Directory
[Name]

NSC-12
[CAS]

102586-30-1
[Synonyms]

CS-2161
CS-2338
NSC-12;NSC 12;NSC12
21-Norchol-5-ene-3,20,23-triol, 24,24,24-trifluoro-23-(trifluoromethyl)-, (3β,20S)-
[Molecular Formula]

C24H34F6O3
[MDL Number]

MFCD31544308
[MOL File]

102586-30-1.mol
[Molecular Weight]

484.52
Chemical PropertiesBack Directory
[Boiling point ]

521.8±45.0 °C(Predicted)
[density ]

1.31±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 2 mg/ml; DMSO: 0.1 mg/ml; Ethanol: 20 mg/ml; Ethanol:PBS (pH 7.2)(1:2): 0.33 mg/ml
[form ]

A crystalline solid
[pka]

9.50±0.29(Predicted)
[color ]

White to light yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS07,GHS09
[Signal word ]

Warning
[Hazard statements ]

H302-H400-H410
[Precautionary statements ]

P264-P270-P273-P301+P312-P330-P391-P501
Hazard InformationBack Directory
[Biological Activity]

NSC12 (NSC 172285) is an orally available inhibitor of FGF2/FGFR interaction with potential antitumor activity.
[in vitro]

NSC-12 can inhibit FGF-dependent tumor growth, angiogenesis and metastasis. It did not affect FGF2/heparin interaction, but inhibited FGF2 binding to immobilized receptors (IC50 ~30 μM), it disrupted FGF2 interaction with FGFR1, and had no effect on the interaction activity of growth factors with heparin or HSPGs .
[in vivo]

Administered by injection and oral route, NSC-12 inhibits FGFR activation, tumor growth, angiogenesis and metastasis in FGF-dependent mouse and human tumor models. In animal models, it significantly reduced tumor weight, tumor cell FGFR1 phosphorylation levels and proliferation, and tumor CD31+ cardiovascular formation.
[target]

TargetValue
FGF3
(Cell-free assay)
15.9 μM(Kd)
FGF8b
(Cell-free assay)
18.9 μM(Kd)
FGF22
(Cell-free assay)
26.8 μM(Kd)
FGF20
(Cell-free assay)
29.4 μM(Kd)
FGF2/FGFR
(Cell-free assay)
30 μM
[storage]

Store at -20°C
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