BT2

9 Cited Publications
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Based on 9 publication(s) in Google Scholar

BT2 is a BCKDC kinase (BDK) inhibitor with an IC50 of 3.19 μM. BT2 binding to BDK triggers helix movements in the N-terminal domain, resulting in the dissociation of BDK from the branched-chain α-ketoacid dehydrogenase complex (BCKDC). BT2 (compound 4) is also a potent and selective Mcl-1 inhibitor with a Ki value of 59 μM.

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  • Reinheit: 99.81%
  • CAS. Nr.: 34576-94-8
  • Formel: C9H4Cl2O2S
  • Molecular Weight:247.10
  • Speicherung:
    Powder   -20°C, 3 years ; In solvent   -80°C, 6 months , -20°C, 1 month
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