产品名称 BT2
产品货号 Axon 2334 CAS [34576-94-8] MF C9H4Cl2O2SMW 247.10 Purity: 99% Soluble in DMSO Description Allosteric inhibitor of branched-chain α-ketoacid dehydrogenase (BCKDC) kinase (BDK; IC50 value 3.19 μM). BT 2 binding to BDK results in the dissociation of BDK from the BCKDC accompanied by accelerated degradation of the released kinase in vivo. BT 2 is also known to inhibit the Bcl-2 family member Mcl-1 (Ki value 59 µM). References Certificates Categories Extra info A. Friberg et al. Discovery of potent myeloid cell leukemia 1 (Mcl-1) inhibitors using fragment-based methods and structure-based design. J. Med. Chem. 2013, 56, 15-30.   S.C. Tso et al. Benzothiophene carboxylate derivatives as novel allosteric inhibitors of branched-chain α-ketoacid dehydrogenase kinase. J. Biol. Chem. 2014, 289, 20583-20593. Certificate of Analysis Material Safety Data Sheet Apoptosis Cell Cycle Regulation Cell Signaling & Oncology Diabetes & Metabolism BDK Mcl-1 EC 2.7.11.4 Allosteric inhibitor of BCKDC kinase (BDK) and Mcl-1 inhibitor Chemical name 3,6-dichlorobenzo[b]thiophene-2-carboxylic acid Parent CAS No. [34576-94-8] Order Size Unit Price Stock 5 mg €95.00 In Stock
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BT2

Based on 8 reference(s) in Google Scholar 9 10 8

Axon 2334

CAS [34576-94-8]

MF C9H4Cl2O2S
MW 247.10

  • Purity: 99%
  • Soluble in DMSO

BT2

Description

Allosteric inhibitor of branched-chain α-ketoacid dehydrogenase (BCKDC) kinase (BDK; IC50 value 3.19 μM). BT 2 binding to BDK results in the dissociation of BDK from the BCKDC accompanied by accelerated degradation of the released kinase in vivo. BT 2 is also known to inhibit the Bcl-2 family member Mcl-1 (Ki value 59 µM).
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