XL647

XL647

CAT N°: 27049
Price:

From 146.00 124.10

XL647 is a multi-kinase inhibitor (IC50s = 0.3, 16, 1.5, 8.7, and 1.4 nM for EGFR, ErbB2, KDR, FLT4, and EphB4, respectively).{45304} It is selective for these kinases over a panel of 10 tyrosine kinases and 55 serine/threonine kinases at 10 ?M. XL647 inhibits growth of A431 cells expressing wild-type EGFR and H1975 non-small cell lung cancer (NSCLC) cells expressing both the activating mutant EGFRL858R and the drug resistance-associated mutant EGFRT790M (IC50s = 13 and 920 nM, respectively). In vivo, XL647 (10, 30, and 100 mg/kg) inhibits tumor growth and EGFR phosphorylation in an H1975 mouse xenograft model in a dose-dependent manner.

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • N-(3,4-dichloro-2-fluorophenyl)-6-methoxy-7-[[(3a?,5?,6a?)-octahydro-2-methylcyclopenta[c]pyrrol-5-yl]methoxy]-4-quinazolinamine
  • Correlated keywords
    • 874286-84-7 950774-05-7 KD 019 KD019 ErbB-2 XL-647 FLT-4 EphB-4 A-431 H-1975 EGFR-L858R EGFR-T790M EXEL7647 multikinase wildtype nonsmall HER2 HER
  • Product Overview:
    XL647 is a multi-kinase inhibitor (IC50s = 0.3, 16, 1.5, 8.7, and 1.4 nM for EGFR, ErbB2, KDR, FLT4, and EphB4, respectively).{45304} It is selective for these kinases over a panel of 10 tyrosine kinases and 55 serine/threonine kinases at 10 ?M. XL647 inhibits growth of A431 cells expressing wild-type EGFR and H1975 non-small cell lung cancer (NSCLC) cells expressing both the activating mutant EGFRL858R and the drug resistance-associated mutant EGFRT790M (IC50s = 13 and 920 nM, respectively). In vivo, XL647 (10, 30, and 100 mg/kg) inhibits tumor growth and EGFR phosphorylation in an H1975 mouse xenograft model in a dose-dependent manner.

We also advise you