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Esprolol

Pharmaceutical compound From Wikipedia, the free encyclopedia

Esprolol, also known as (S)-ACC-9369, is a beta blocker which was under development for the treatment of angina pectoris, anxiety disorders, and migraine.[1][3][2] It is taken sublingually and has a rapid onset of action, short time to peak, and short duration.[1][2] The drug is a prodrug of amoxolol, which is formed from esprolol via esterase enzymes.[2] It is a selective β1-adrenergic receptor antagonist.[2][4] Esprolol was under development by Selectus Pharmaceuticals.[1][3] It reached phase 2 clinical trials for all indications prior to the discontinuation of its development in 2001.[1][3]

Other names(S)-ACC-9369; (S)-ACC9369
ATC code
  • None
Quick facts Clinical data, Other names ...
Esprolol
Clinical data
Other names(S)-ACC-9369; (S)-ACC9369
Routes of
administration
Sublingual[1][2]
Drug classBeta blocker; β1-Adrenergic receptor antagonist
ATC code
  • None
Pharmacokinetic data
MetabolismEsterases[2]
MetabolitesAmoxolol[2]
Onset of action"Rapid"[1][2]
Duration of action"Short"[2]
Identifiers
  • ethyl 3-[2-[(2S)-2-hydroxy-3-(propan-2-ylamino)propoxy]phenyl]propanoate
CAS Number
PubChem CID
ChemSpider
UNII
Chemical and physical data
FormulaC17H27NO4
Molar mass309.406 g·mol−1
3D model (JSmol)
  • CCOC(=O)CCC1=CC=CC=C1OC[C@H](CNC(C)C)O
  • InChI=1S/C17H27NO4/c1-4-21-17(20)10-9-14-7-5-6-8-16(14)22-12-15(19)11-18-13(2)3/h5-8,13,15,18-19H,4,9-12H2,1-3H3/t15-/m0/s1
  • Key:DMLSVZSUDBKLED-HNNXBMFYSA-N
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