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SC 144

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SC 144 Basic information

Product Name:
SC 144
Synonyms:
  • 2-Pyrazinecarboxylic acid, 2-(7-fluoropyrrolo[1,2-a]quinoxalin-4-yl)hydrazide
  • 2-(7-fluoropyrrolo[1,2-a]quinoxalin-4-yl)hydrazide
  • SC 144
  • SC144
  • SC-144
  • Pyrazinecarboxylic acid 2-(7-fluoropyrrolo[1,2-a]quinoxalin-4-yl)hydrazide
  • SC 144; SC144
  • CS-805
CAS:
895158-95-9
MF:
C16H11FN6O
MW:
322.3
Product Categories:
  • Inhibitors
Mol File:
895158-95-9.mol
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SC 144 Chemical Properties

Density 
1.53±0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
insoluble in EtOH; insoluble in H2O; ≥16.1 mg/mL in DMSO
form 
solid
pka
8.87±0.43(Predicted)
color 
Light yellow to yellow
InChI
InChI=1S/C16H11FN6O/c17-10-3-4-13-11(8-10)20-15(14-2-1-7-23(13)14)21-22-16(24)12-9-18-5-6-19-12/h1-9H,(H,20,21)(H,22,24)
InChIKey
UEADAWQSJOWXBK-UHFFFAOYSA-N
SMILES
C1(C(NNC2=NC3=C(N4C=CC=C42)C=CC(F)=C3)=O)=NC=CN=C1
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SC 144 Usage And Synthesis

Uses

SC144 is an orally active small-molecule gp130 inhibitor.

Biological Activity

sc144 is an inhibitor of gp130 with ic50 values of 0.43 μmol/l and 0.88 μmol/l in nci/adr-res and hey cell lines, respectively [1].sc144 is a first-in-class small-molecule gp130 inhibitor with oral activity in ovarian cancer. it can substantially increase the phosphorylation of gp130 (s782) in both ovcar-8 and caov-3 cells in a time- and dose-dependent manner. the increase phosphorylation then suppresses stat3 signaling pathway since the constitutive stat3 activation is maintained by extracellular gp130 ligands, besides that, sc144 also causes substantial cell apoptosis in these cells. [1].apart from the effect on gp130, it has been reported that sc144 can directly bind and stabilize il-24 in cancer cells. additionally, sc144 has shown to have effects on cell cycle perturbation and apoptosis induction [2].sc144 may also have other cellular protein targets, resulting in multiple potential molecular mechanisms. sc144’s anticancer potency may be a sum of these effects [2].

in vivo

SC144 (10 mg/kg; i.p.; daily for 58 days) suppresses tumor growth in human ovariancancer xenografts[1].
? SC144 (100 mg/kg;p.o.; daily for 35 days) treatment shows the average tumor volume in mice 82% smaller than that in the control group[1].

Animal Model:Athymic mice (human ovarian cancer xenograft)[1]
Dosage:10 mg/kg
Administration:I.p; daily for 58 days
Result:Significantly inhibited tumor growth by about 73%.

IC 50

IL6-beta

References

[1] shili xu, fedora grande, antonio garofalo, et al. discovery of a novel orally active small-molecule gp130 inhibitor for the treatment of ovarian cancer. molecular cancer therapeutics. 2013 (12): 937-949.
[2] shili xu, takashi oshima, toshio imada, munetaka masuda, bikash debnath, fedora grande, antonio garofalo, nouri neamati. stabilization of mda-7/il-24 for colon cancer therapy. cancer letters. 2013 feb(335):421-430.

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