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TYRPHOSTIN A9

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TYRPHOSTIN A9 Basic information

Product Name:
TYRPHOSTIN A9
Synonyms:
  • ALPHA-CYANO-(3,5-DI-T-BUTYL-4-HYDROXY)CINNAMONITRILE
  • TYRPHOSTIN A9 \ SELECTIVE PDGF TYROSINE
  • TYRPHOSTIN A9 99+%
  • Malonobene
  • 2-(3,5-di-tert-butyl-4-hydroxybenzylidene)Malononitrile
  • Tyrphostin 9 (SF 6847)
  • Propanedinitrile, 2-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-
  • [[3,5-BIS(1,1-DIMETHYLETHYL)-4-HYDROXYPHENYL]METHYLENE]-PROPANEDINITRILE
CAS:
10537-47-0
MF:
C18H22N2O
MW:
282.38
Product Categories:
  • Inhibitors
Mol File:
10537-47-0.mol
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TYRPHOSTIN A9 Chemical Properties

Melting point:
141-143℃ (ethanol )
Boiling point:
424.99°C (rough estimate)
Density 
1.0741 (rough estimate)
refractive index 
1.5700 (estimate)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
ethanol: 20 mg/mL
form 
solid
pka
7.55±0.40(Predicted)
color 
yellow
Stability:
Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 3 months.
CAS DataBase Reference
10537-47-0(CAS DataBase Reference)
EPA Substance Registry System
Malonoben (10537-47-0)
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Safety Information

Hazard Codes 
T
Risk Statements 
23/24/25
Safety Statements 
36/37/39-45
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
RTECS 
OO3737000
HS Code 
2926.90.5050
HazardClass 
6.1

MSDS

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TYRPHOSTIN A9 Usage And Synthesis

Description

Tyrphostin 9 (10537-47-0) inhibits PDGF receptor tyrosine kinase (IC50?= 1.2 μM)1and is a potent (10 nM) inhibitor of oxidative phosphorylation2. Inhibits cell growth by disrupting mitochondria.3 Tyrphostin 9 perturbs the golgi complex and blocks proliferation of vascular smooth muscle cells.4

Uses

Tyrphostin A9 can be used for inhibiting tyrosine kinase functions in C2C12 cells. It has also been used to disrupt membrane potential in mammalian cells.

Uses

SF 6847 is an inhibitor of EGFR with IC50 of 460 μM.

Uses

Selective inhibitor of PDGF receptor tyrosine kinase

Definition

ChEBI: Malonoben is an alkylbenzene. It has a role as a geroprotector.

General Description

A selective, cell-permeable, reversible, and substrate competitive inhibitor of the platelet-derived growth factor receptor tyrosine kinase (IC50 = 500 nM). Anti-proliferative agent. Uncoupler of oxidative phosphorylation. Induces apoptosis in vitro and cell growth arrest in NHL cell lines.

Biological Activity

Potent uncoupler of oxidative phosphorylation.

Biochem/physiol Actions

Cell permeable: yes

References

1) Bilder?et al. (1991),?Tyrphostins inhibit PDGF-induced DNA synthesis and associated early events in smooth muscle cells; Am. J. Physiol.,?260?C721 2) Terada?et al. (1981),?The interaction of highly active uncouplers with mitochondria; Biochim. Biophys. Acta,?639?225 3) Burger?et al. (1995),?Tyrphostin AG17, [3,5-Ditert-butyl-4-hydroxybenzylidene)-malononitrile], inhibits cell growth by disrupting mitochondria; Cancer Res.,?55?2794 4) Thyberg?et al. (1998),?Tyrphostin A9 and wortmannin perturb the Golgi complex and block proliferation of vascular smooth muscle cells; Eur. J. Cell Biol.,?76?33

TYRPHOSTIN A9Supplier

3B Pharmachem (Wuhan) International Co.,Ltd.
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821-50328103-801 18930552037
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3bsc@sina.com
TCI (Shanghai) Development Co., Ltd.
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021-67121386
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Adamas Reagent, Ltd.
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400-6009262 16621234537
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zhangsn@titansci.com
Jinan Trio PharmaTech Co., Ltd.
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+86 (531) 88811783
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sales@trio-pharmatech.com (International market)
Spectrum Chemical Manufacturing Corp.
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021-021-021-67601398-809-809-809 15221380277
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marketing_china@spectrumchemical.com