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Medchemexpress LLC BI-882370 | 1392429-79-6 | MFCD31618072 | 99.2% | 569.67 | C28H33F2N7O2S | 5 MG
SDP

Catalog No. 5000240317
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BI-882370 is a potent, selective small-molecule pan-RAF kinase inhibitor that binds the ATP binding site in the DFG-out (inactive) conformation. It demonstrates sub-nanomolar to low-nanomolar inhibition of BRAF V600E, wild-type BRAF, and CRAF, and is supplied as a high-purity solid for preclinical research applications.

  • Potent pan-RAF inhibition with sub-nanomolar to low-nanomolar potency.
  • Binds the ATP site in the DFG-out inactive conformation.
  • High purity solid suitable for in vitro and in vivo preclinical studies.
  • Well-defined chemical identity with confirmed molecular formula and mass.
  • Available in small research-scale packaging for dose response experiments.

Catalog No. 50-002-40317 Supplier Medchemexpress LLC Supplier No. HY1077795MG
May include imposed supplier surcharges.
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BI-882370 is a potent, selective small-molecule pan-RAF kinase inhibitor that binds the ATP binding site in the DFG-out (inactive) conformation. It demonstrates sub-nanomolar to low-nanomolar inhibition of BRAF V600E, wild-type BRAF, and CRAF, and is supplied as a high-purity solid for preclinical research applications.

  • Potent pan-RAF inhibition with sub-nanomolar to low-nanomolar potency.
  • Binds the ATP site in the DFG-out inactive conformation.
  • High purity solid suitable for in vitro and in vivo preclinical studies.
  • Well-defined chemical identity with confirmed molecular formula and mass.
  • Available in small research-scale packaging for dose response experiments.

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