| Bioactivity | (S)-BAY 2965501 is the left-handed isomer of BAY 2965501 (HY-153343). BAY 2965501 is a potent and selective diacylglycerol kinase zeta (DGKζ) inhibitor. BAY 2965501 induces pERK activation. BAY 2965501 can be used for the research of cancer[1]. | |||||||||
| Target | DGKz | |||||||||
| Name | (S)-BAY 2965501 | |||||||||
| CAS | 2732902-09-7 | |||||||||
| Formula | C20H19FN4O3S | |||||||||
| Molar Mass | 414.45 | |||||||||
| Appearance | Solid | |||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | |||||||||
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| Reference | [1]. Schubert N, et al. Phosphorylated extracellular signal-regulated kinase (pERK) activation in T effector cells as a target engagement biomarker for the DGK味 inhibitor BAY2965501 in clinical trials. Cancer Research, 2023, 83(7_Supplement): 2116-2116. |
(S)-BAY 2965501
CAS: 2732902-09-7 F: C20H19FN4O3S W: 414.45
(S)-BAY 2965501 is the left-handed isomer of BAY 2965501 (HY-153343). BAY 2965501 is a potent and selective diacylglycer
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