Details
| Stereochemistry | MIXED |
| Molecular Formula | C21H32NO3 |
| Molecular Weight | 346.4837 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 0 / 3 |
| E/Z Centers | 0 |
| Charge | 1 |
SHOW SMILES / InChI
SMILES
C[N+]1(C)CCCC1COC(=O)C(O)(C2CCCCC2)C3=CC=CC=C3
InChI
InChIKey=KASKRXOORXMTTP-UHFFFAOYSA-N
InChI=1S/C21H32NO3/c1-22(2)15-9-14-19(22)16-25-20(23)21(24,17-10-5-3-6-11-17)18-12-7-4-8-13-18/h3,5-6,10-11,18-19,24H,4,7-9,12-16H2,1-2H3/q+1
| Molecular Formula | C21H31NO3 |
| Molecular Weight | 345.4757 |
| Charge | 0 |
| Count |
|
| Stereochemistry | MIXED |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Oxypyrronium is an anticholinergic and spasmolytic agent containing quaternary ammonium. In animal models it inhibited gastric motility, hypotension induced by vagus stimulation or intravenation of acetylcholine; salivation induced by chorda tympani nerve stimulation, and contraction elicited by preganglionic cervical sympathetic nerve stimulation. Oxypyrronium was marketed in France under tradename Immetropan for the treatment of gastric pain.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:32:26 GMT 2025
by
admin
on
Mon Mar 31 21:32:26 GMT 2025
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| Record UNII |
1IH4C995X0
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| Record Status |
Validated (UNII)
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| Record Version |
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1IH4C995X0
Created by
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71508
Created by
admin on Mon Mar 31 21:32:26 GMT 2025 , Edited by admin on Mon Mar 31 21:32:26 GMT 2025
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116533-64-3
Created by
admin on Mon Mar 31 21:32:26 GMT 2025 , Edited by admin on Mon Mar 31 21:32:26 GMT 2025
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