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T4182

Sigma-Aldrich

Tyrphostin AG 1478

≥98%

Sinonimo/i:

N-(3-Chlorophenyl)-6,7-dimethoxy-4-quinazolinamine

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About This Item

Formula empirica (notazione di Hill):
C16H14ClN3O2
Numero CAS:
Peso molecolare:
315.75
Numero MDL:
Codice UNSPSC:
51111800
ID PubChem:
NACRES:
NA.77

Livello qualitativo

Saggio

≥98%

Forma fisica

solid

Solubilità

0.1 M HCl: soluble <0.4 mg/mL
DMSO:methanol (1:1): soluble 10 mg/mL, clear, colorless
ethanol: soluble 10 mg/mL
methylene chloride: soluble 10 mg/mL
0.1 M NaOH: insoluble
2-hydroxypropyl-β-cyclodextrin: insoluble
H2O: insoluble

Temperatura di conservazione

2-8°C

Stringa SMILE

COc1cc2ncnc(Nc3cccc(Cl)c3)c2cc1OC

InChI

1S/C16H14ClN3O2/c1-21-14-7-12-13(8-15(14)22-2)18-9-19-16(12)20-11-5-3-4-10(17)6-11/h3-9H,1-2H3,(H,18,19,20)
GFNNBHLJANVSQV-UHFFFAOYSA-N

Informazioni sul gene

human ... EGFR(1956)
mouse ... Egfr(13649)

Applicazioni

Tyrphostin AG 1478 has been used as epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor to study its effect on desmoid cell mobility in boyden chamber motility assays. It has also been used to inhibit phosphorylation of c-Met by exogenous transforming growth factor α in epidermoid carcinoma cell line A431.

Azioni biochim/fisiol

Tyrphostin AG 1478 is an epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor. It contributes to the development of hypomagnesemia and cardiac dysfunction in rats. Tyrphostin AG 1478 acts as a potential therapeutic agent for breast cancer.
Selective inhibitor of epidermal growth factor receptor protein

Caratteristiche e vantaggi

This compound is a featured product for Kinase Phosphatase Biology research. Click here to discover more featured Kinase Phosphatase Biology products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound is featured on the EGFR page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Nota sulla preparazione

Tyrphostin AG 1478 dissolves in DMSO:MeOH (1:1) at 10 mg/ml to yield a clear, colorless solution. It is also soluble in methylene chloride (10 mg/ml), ethanol (10 mg/ml) and 0.1 N HCl (less than 0.4 mg/ml). However, it is insoluble in water, 2-hydroxypropyl-β-cyclodextrin, and 0.1 N NaOH.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


Certificati d'analisi (COA)

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I clienti hanno visto anche

Desmoid cell motility is induced in vitro by rhEGF
Joyner DE, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society, 27(9), 1258-1262 (2009)
Y Han et al.
Cancer research, 56(17), 3859-3861 (1996-09-01)
The effects of a new epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor, tyrphostin AG 1478, were tested on three related human glioma cell lines: U87MG, which expressed endogenous wild-type (wt) EGFR, and two retrovirally infected U87MG cell populations which
Tyrphostin AG 1478 preferentially inhibits human glioma cells expressing truncated rather than wild-type epidermal growth factor receptors
Han Y, et al.
Cancer Research, 56, 3859-3861 (2019)
The EGFR tyrosine kinase inhibitor tyrphostin AG-1478 causes hypomagnesemia and cardiac dysfunction
Weglicki WB, et al.
Canadian Journal of Physiology and Pharmacology, 56, 8-8 (2019)
Tyrphostin AG1478 suppresses proliferation and invasion of human breast cancer cells.
Zhang YG, et al.
International Journal of Oncology, 33(3), 595-602 (2008)

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