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Medchemexpress LLC 2-chloro-4-((1R)-1-(4-(4-fluoro-2-oxopyridin-1(2H)-yl)phenyl)ethylamino)-N-(5-(trifluoromethyl)pyridin-2-yl)... | 871026-44-7 | MFCD22124520 | 99.0% | 547.96 | C26H25ClF3N5O3 | 10 MG
SDP

Catalog No. 5000287511
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TAK-285 is a potent, selective, ATP-competitive, orally active inhibitor of HER2 and EGFR (HER1) used in oncology and kinase research. It exhibits low-nanomolar potency against HER2 and EGFR, shows selectivity over related kinases, and has demonstrated antitumor activity with the ability to cross the blood-brain barrier.

  • Potent ATP-competitive inhibitor of HER2 and EGFR with low-nanomolar IC50 values.
  • Greater than 10-fold selectivity for HER1/2 compared with HER4.
  • Demonstrated antitumor activity and ability to penetrate the blood-brain barrier.
  • High purity suitable for biochemical and cellular assays.
  • Available as solid packs and as a 10 mM solution in DMSO for stock preparation.
  • Well characterized by molecular formula and molecular weight for compound verification.

Catalog No. 50-002-87511 Supplier Medchemexpress LLC Supplier No. HY1519610MG
May include imposed supplier surcharges.
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TAK-285 is a potent, selective, ATP-competitive, orally active inhibitor of HER2 and EGFR (HER1) used in oncology and kinase research. It exhibits low-nanomolar potency against HER2 and EGFR, shows selectivity over related kinases, and has demonstrated antitumor activity with the ability to cross the blood-brain barrier.

  • Potent ATP-competitive inhibitor of HER2 and EGFR with low-nanomolar IC50 values.
  • Greater than 10-fold selectivity for HER1/2 compared with HER4.
  • Demonstrated antitumor activity and ability to penetrate the blood-brain barrier.
  • High purity suitable for biochemical and cellular assays.
  • Available as solid packs and as a 10 mM solution in DMSO for stock preparation.
  • Well characterized by molecular formula and molecular weight for compound verification.

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