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Medchemexpress LLC N-(3-(5-((1-Ethylpiperidin-4-yl)(methyl)amino)-3-(pyrimidin-5-yl)-1H-pyrrolo[3,2-b]pyridin-1-yl)-... | 1392429-79-6 | MFCD31618072 | 99.2% | 569.67 | C28H33F2N7O2S | 50 MG
SDP

Catalog No. 5000240830
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BI-882370 is a selective pan-RAF kinase inhibitor research compound for preclinical kinase and cellular studies. It binds the ATP site of RAF kinases in the DFG-out conformation and exhibits sub-nanomolar biochemical potency against BRAFV600E, wild-type BRAF, and CRAF. Supplied as a high-purity solid, it is intended for in vitro and in vivo pharmacology and assay development.

  • High purity solid suitable for assays and preclinical work.
  • Sub-nanomolar biochemical potency against BRAFV600E, BRAF, and CRAF.
  • Binds RAF kinases in the DFG-out (inactive) conformation.
  • Available in multiple small pack sizes for research use.
  • Provided with molecular and spectral identifiers for reference.

Catalog No. 50-002-40830 Supplier Medchemexpress LLC Supplier No. HY10777950MG
May include imposed supplier surcharges.
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BI-882370 is a selective pan-RAF kinase inhibitor research compound for preclinical kinase and cellular studies. It binds the ATP site of RAF kinases in the DFG-out conformation and exhibits sub-nanomolar biochemical potency against BRAFV600E, wild-type BRAF, and CRAF. Supplied as a high-purity solid, it is intended for in vitro and in vivo pharmacology and assay development.

  • High purity solid suitable for assays and preclinical work.
  • Sub-nanomolar biochemical potency against BRAFV600E, BRAF, and CRAF.
  • Binds RAF kinases in the DFG-out (inactive) conformation.
  • Available in multiple small pack sizes for research use.
  • Provided with molecular and spectral identifiers for reference.

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