| Identification | Back Directory | [Name]
(4S)-3,4-Dihydro-4-phenyl-3-[1-[[3-(trifluoromethoxy)phenyl]methyl]-4-piperidinyl]-2(1H)-quinazolinone | [CAS]
877606-63-8 | [Synonyms]
NS986 NS-986 SMP986 NS 986 SMP-986 SMP 986 Afacifenacin Afacifenacin Fumarate (4S)-3,4-Dihydro-4-phenyl-3-[1-[[3-(trifluoromethoxy)phenyl]methyl]-4-piperidinyl]-2(1H)-quinazolinone 2(1H)-Quinazolinone, 3,4-dihydro-4-phenyl-3-[1-[[3-(trifluoromethoxy)phenyl]methyl]-4-piperidinyl]-, (4S)- | [Molecular Formula]
C27H26F3N3O2 | [MDL Number]
MFCD16619353 | [MOL File]
877606-63-8.mol | [Molecular Weight]
481.51 |
| Hazard Information | Back Directory | [Uses]
Afacifenacin acts as a sodium/calcium exchanger inhibitor used in the prevention of reperfusion injury associated with restoration of coronary blood flow via surgery. | [in vivo]
Afacifenacin (0.3, 1, 3 mg/kg; Intragastric administration) significantly increases bladder capacity and reduced micturition pressure (MP) in cerebral infarction rats[2]. | Animal Model: | Male Sprague-Dawley rats (cerebral infarction model)[2] | | Dosage: | 0.3, 1, 3 mg/kg | | Administration: | Intragastric administration | | Result: | Significantly increased bladder capaticy and reduced micturition pressure (MP) without affecting residual urinary volume (RUV). |
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