Tyrphostin AG 1112

Modify Date: 2024-01-12 19:22:37

Tyrphostin AG 1112 Structure
Tyrphostin AG 1112 structure
Common Name Tyrphostin AG 1112
CAS Number 153150-84-6 Molecular Weight 274.28
Density N/A Boiling Point N/A
Molecular Formula C15H10N6 Melting Point N/A
MSDS USA Flash Point N/A

 Use of Tyrphostin AG 1112


Tyrphostin AG1112 is a potent inhibitors of CK II. Tyrphostin AG1112 inhibits p210bcr-abl tyrosine kinase, with IC50 values of 2, 15, 20 μM in p210bcr-abl, EGFR and PDGFR cells, respectively[1][2].

 Names

Name TYRPHOSTIN AG 1112

 Tyrphostin AG 1112 Biological Activity

Description Tyrphostin AG1112 is a potent inhibitors of CK II. Tyrphostin AG1112 inhibits p210bcr-abl tyrosine kinase, with IC50 values of 2, 15, 20 μM in p210bcr-abl, EGFR and PDGFR cells, respectively[1][2].
Related Catalog
In Vitro Tyrphostin AG1112 (0-100 μM) dose-dependently induces differentiation also induce specific growth arrest[1].
References

[1]. T B Kang, et al. Action of 3 tyrphostin derivatives on casein kinase II from rat liver. Zhongguo Yao Li Xue Bao. 1997 Jan;18(1):56-8.  

[2]. M Anafi, et al. Tyrphostin-induced inhibition of p210bcr-abl tyrosine kinase activity induces K562 to differentiate. Blood. 1993 Dec 15;82(12):3524-9.  

 Chemical & Physical Properties

Molecular Formula C15H10N6
Molecular Weight 274.28
Appearance of Characters solid
Storage condition −20°C

 Safety Information

Hazard Codes Xn
Risk Phrases 36/37/38-40
Safety Phrases 26-36/37
RIDADR NONH for all modes of transport
WGK Germany 1

 Articles2

More Articles
Protein kinase inhibitors as a therapeutic modality.

Acc. Chem. Res. 36(6) , 462-9, (2003)

Most of the signal transduction pathways are mediated by protein kinases regulating every aspect of cell function. Mutations which deregulate their expression or their function or both result in cance...

Tyrphostin-induced inhibition of p210bcr-abl tyrosine kinase activity induces K562 to differentiate.

Blood 82(12) , 3524-9, (1993)

We report on the potency of two Tyrphostin tyrosine kinase blockers, AG 1112 and AG 568, to inhibit p210bcr-abl tyrosine kinase activity in K562 cells, concomitant with the induction of erythroid diff...

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