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Tyrphostin AG 879

Chemical Structure : Tyrphostin AG 879

CAS No.: 148741-30-4

Tyrphostin AG 879 (AG-879, AG879)

Catalog No.: PC-45785Not For Human Use, Lab Use Only.

Tyrphostin AG 879 (AG879) potent HER2/ErbB2 inhibitor with IC50 of 1 uM, also selecitvely inhibits TrKA phosphorylation with IC50 of 10 uM, but not TrKB and TrKC.

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5 mg (Free Sample) $28 In stock
25 mg $128 In stock
50 mg $198 In stock
100 mg $328 In stock
250 mg Get quote

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

Tyrphostin AG 879 (AG879) potent HER2/ErbB2 inhibitor with IC50 of 1 uM, also selecitvely inhibits TrKA phosphorylation with IC50 of 10 uM, but not TrKB and TrKC.
Tyrphostin AG 879 is 100- and 500-fold higher selective to ErbB2 than PDGFR and EGFR.
Tyrphostin AG 879 inhibits growth of FET6αS26X cells in a concentration-dependent manner.
Tyrphostin AG 879 blocks the activation of PAK1 and suppresses RAS-induced malignant transformation of NIH 3T3 cells.
Tyrphostin AG 879 reduces the size of the growing sarcomas in the nude mice carrying v-Ha-RAS transformed NIH 3T3 cells.

Physicochemical Properties

M.Wt 316.461
Formula C18H24N2OS
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

DMSO: ≥ 30 mg/mL

Chemical Name/SMILES

2-Propenethioamide, 3-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]-2-cyano-, (2E)-

References

1. Ohmichi M, et al. Biochemistry. 1993 May 4;32(17):4650-8.

2. Zhou Y, et al. Cancer Res. 2005 Jul 1;65(13):5848-56.

3. He H, et al. Cancer J. 2001, 7(3), 191-202.

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