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BET Bromodomains

Ref-Nr: TA-2252


Kurzfassung

Highly Efficient and Selective Inhibitors Targeting BET Bromodomains


Hintergrund

BET proteins are important because they regulate both normal transcription processes as well as the transcription of oncogenes such as c-myc and Bcl-2 in various types of cancer. An efficient and selective inhibition of the BET proteins is therefore of great importance for cancer therapies. Various compounds, including benzenesulfonamide derivates are known to possess this property. However, there is a great desire for further, more selective inhibitors.


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Lösung

The use of sulfoximine, sulfondiimide and sulfonimidamide derivatives allows to generate novel molecules with a stereogenic sulfur atom. The utilization of this chirality provides new, highly effective and selective BET inhibitors.


Vorteile

  • Novel BET inhibitors bearing a stereocenter
  • Chirality is the key to high efficacy and selectivity

Anwendungsbereiche

Pharmaceutical Development; Oncology


Service

  • International patent application pending and German patent application pending.
  •  Proof of concept and Ongoing research

 

RWTH Aachen University is looking for partners for patent exploitation.


RWTH Aachen

Marieke Sternkopf
0241 8096612
ipm@rwth-aachen.de
www.rwth-innovation.de
Adresse
Campus-Boulevard 57
52074 Aachen



Stichworte

#BET inhibitor, #Sulfoximines, #Sulfondiimides, #Sulfonimidam-ides

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