Chemical Structure : Tyrphostin AG 879
CAS No.: 148741-30-4
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.
Packing | Price | Stock | Quantity |
---|---|---|---|
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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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.
M.Wt | 316.461 | |
Formula | C18H24N2OS | |
Appearance | Solid | |
Storage |
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Solubility |
DMSO: ≥ 30 mg/mL |
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Chemical Name/SMILES |
2-Propenethioamide, 3-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]-2-cyano-, (2E)- |
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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