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Apatinib Mesylate

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Apatinib Mesylate Basic information

Product Name:
Apatinib Mesylate
Synonyms:
  • Apatinib Mesylate(YN968D1)
  • Apatinib methanesulfonate
  • N-(4-(1-cyanocyclopentyl)phenyl)-2-((pyridin-4-ylmethyl)amino)nicotinamide methanesulfonic acid
  • N-[4-(1-Cyanocyclopentyl)phenyl]-2-[(4-pyridinylmethyl)amino]-3-pyridinecarboxamide methanesulfonate
  • YN 968D1
  • N-[4-(1-Cyanocyclopentyl)phenyl]-2-[(4-pyridinylmethyl)amino]-3-pyridinecarboxamide methanesulfonate ISO 9001:2015 REACH
  • Pyrazino[2,3-f][1,14]phenanthroline
  • Apatinib Mesylate
CAS:
1218779-75-9
MF:
C25H27N5O4S
MW:
493.58
EINECS:
1592732-453-0
Mol File:
1218779-75-9.mol
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Apatinib Mesylate Chemical Properties

storage temp. 
Store at -20°C
solubility 
≥49.4 mg/mL in DMSO; insoluble in H2O; ≥2.17 mg/mL in EtOH with gentle warming and ultrasonic
form 
solid
Water Solubility 
Water: Insoluble
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Apatinib Mesylate Usage And Synthesis

Biological Activity

apatinib (yn968d1)is a potent inhibior of the vegf signaling pathway with the ic50 value of 1nm for vegfr-2 in in vitro enzyme experiments [1]..

in vitro

apatinib has shown the inhibition of tyrosine kinase activities with the ic50 values of 0.013μm, 0.429μm and 0.53μm for ret, c-kit and c-src, respectively. in addition, apatinib has been revealed to have no significant effects in egfr, her-2 or fgfr1 in concentrations up to 10μm. apart from these, apatinib has been reported to inhibit the growth factor-stimulated receptor phosphorylation at the cellular level. furthermore, apatinib has also reported to slightly inhibitor proliferation of huvec by 20% fbs with the ic50 value of 23.4μm and significantly inhibit stimulated by 20ng/ml vegf with the ic50 value of 0.17μm. once-daily oral administration of apatinib has been noted to produce a dose-dependent inhibition of tumor growth in human tumor xenografts in immunodeficient mice [1]

References

[1] tian s1, quan h, xie c, guo h, lü f, xu y, li j, lou l. yn968d1 is a novel and selective inhibitor of vascular endothelial growth factor receptor-2 tyrosine kinase with potent activity in vitro and in vivo. cancer sci. 2011 jul;102(7):1374-80.

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