| Bioactivity | (S)-BAY 73-6691 is the inactive isomer of BAY 73-6691 (HY-104028), and can be used as an experimental control. BAY 73-6691 ((R)-BAY 73-6691) is a potent, brain penetrant, and selective PDE9A inhibitor[1]. | ||||||||||||
| Name | (S)-BAY 73-6691 | ||||||||||||
| CAS | 794568-91-5 | ||||||||||||
| Formula | C15H12ClF3N4O | ||||||||||||
| Molar Mass | 356.73 | ||||||||||||
| Appearance | Solid | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
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| Reference | [1]. Li J, et al. Protective effects of BAY 73-6691, a selective inhibitor of phosphodiesterase 9, on amyloid-β peptides-induced oxidative stress in in-vivo and in-vitro models of Alzheimer's disease. Brain Res. 2016 Jul 1;1642:327-335. |
(S)-BAY 73-6691
CAS: 794568-91-5 F: C15H12ClF3N4O W: 356.73
(S)-BAY 73-6691 is the inactive isomer of BAY 73-6691 (HY-104028), and can be used as an experimental control. BAY 73-66
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