Empesertib

Empesertib

Empesertib
Identifiers
  • (2R)-2-(4-fluorophenyl)-N-[4-[2-(2-methoxy-4-methylsulfonylanilino)-[1,2,4]triazolo[1,5-a]pyridin-6-yl]phenyl]propanamide
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC29H26FN5O4S
Molar mass559.62 g·mol−1
3D model (JSmol)
  • C[C@H](C1=CC=C(C=C1)F)C(=O)NC2=CC=C(C=C2)C3=CN4C(=NC(=N4)NC5=C(C=C(C=C5)S(=O)(=O)C)OC)C=C3
  • InChI=1S/C29H26FN5O4S/c1-18(19-4-9-22(30)10-5-19)28(36)31-23-11-6-20(7-12-23)21-8-15-27-33-29(34-35(27)17-21)32-25-14-13-24(40(3,37)38)16-26(25)39-2/h4-18H,1-3H3,(H,31,36)(H,32,34)/t18-/m1/s1
  • Key:NRJKIOCCERLIDG-GOSISDBHSA-N

Empesertib (BAY1161909) is an experimental drug which acts as a selective inhibitor of the enzyme monopolar spindle 1 kinase (MPS1). It is in clinical trials for the treatment of breast cancer.[1][2]

References

  1. ^ Wang S, Zhang M, Liang D, Sun W, Zhang C, Jiang M, et al. (August 2019). "Molecular design and anticancer activities of small-molecule monopolar spindle 1 inhibitors: A Medicinal chemistry perspective". European Journal of Medicinal Chemistry. 175: 247–268. doi:10.1016/j.ejmech.2019.04.047. PMID 31121430.
  2. ^ Schulze VK, Klar U, Kosemund D, Wengner AM, Siemeister G, Stöckigt D, et al. (August 2020). "Treating Cancer by Spindle Assembly Checkpoint Abrogation: Discovery of Two Clinical Candidates, BAY 1161909 and BAY 1217389, Targeting MPS1 Kinase". Journal of Medicinal Chemistry. 63 (15): 8025–8042. doi:10.1021/acs.jmedchem.9b02035. PMID 32338514.

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