BAY-876 is an orally active and selective glucose transporter 1 (GLUT1) inhibitor with an IC50 of 2 nM. BAY-876 is >130-fold more selective for GLUT1 than GLUT2, GLUT3, and GLUT4[1]. BAY-876 is also a potent blocker of glycolytic metabolism and ovarian c
Molecular Weight:
496.42
Purity:
98.46
CAS Number:
[1799753-84-6]
Formula:
C24H16F4N6O2
Target:
GLUT
Application Notes:
Reference compound
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