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ST-271

Names

[ CAS No. ]:
106392-48-7

[ Name ]:
ST-271

[Synonym ]:
st 271
ST-271
ST271

Biological Activity

[Description]:

ST271 is a potent inhibitor of protein tyrosine kinase (PTK).

[Related Catalog]:

Signaling Pathways >> Others >> Others
Research Areas >> Others

[In Vitro]

ST271 partially inhibits peptide phosphorylation in the membrane preparation and in permeabilized platelets[1]. ST271 (100 μM) causes complete inhibition of formation of inositol phosphates induced by FcγRII cross-linking, but also induces a small (< 30%) but significant inhibition of the response to thrombin and U46619[2].

[References]

[1]. Martinson EA, et al. Inhibition of phospholipase D of human platelets by protein tyrosine kinase inhibitors. Cell Mol Biol (Noisy-le-grand). 1994 Jul;40(5):627-34.

[2]. Blake RA, et al. Fc gamma receptor II stimulated formation of inositol phosphates in human platelets is blocked by tyrosine kinase inhibitors and associated with tyrosine phosphorylation of the receptor.


[Related Small Molecules]

Captisol | Cyclosporin A | H2DCFDA | 0MPTP hydrochloride | GW4869 | Etomoxir | TD139 | Mitoquinone mesylate | GSK2795039 | JC-1 | BAPTA-AM | AP 20187 | Setanaxib (GKT137831) | D-Luciferin | Crotaline

Chemical & Physical Properties

[ Density]:
1.137g/cm3

[ Boiling Point ]:
468.4ºC at 760mmHg

[ Molecular Formula ]:
C16H20N2O2

[ Molecular Weight ]:
272.34200

[ Flash Point ]:
237.1ºC

[ Exact Mass ]:
272.15200

[ PSA ]:
88.10000

[ LogP ]:
4.18098

[ Appearance of Characters ]:
light yellow solid

[ Vapour Pressure ]:
2.14E-09mmHg at 25°C

[ Index of Refraction ]:
1.585

[ Storage condition ]:
-20℃

Safety Information

[ HS Code ]:
2926909090

Customs

[ HS Code ]: 2926909090

[ Summary ]:
HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%


Related Compounds