Apatinib Mesylate
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
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
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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