Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C20H27NO3 |
| Molecular Weight | 329.4333 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCNCC#CCOC(=O)C(O)(C1CCCCC1)C2=CC=CC=C2
InChI
InChIKey=SNIBJKHIKIIGPR-UHFFFAOYSA-N
InChI=1S/C20H27NO3/c1-2-21-15-9-10-16-24-19(22)20(23,17-11-5-3-6-12-17)18-13-7-4-8-14-18/h3,5-6,11-12,18,21,23H,2,4,7-8,13-16H2,1H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| [Effect of 4-ethylamino-2-butynyl(2-cyclohexyl-2-phenyl) glycolate, metabolite of oxybutynin, on intra-artery administered acetylcholine-induced urinary bladder contraction in anesthetized dogs]. | 2004-05 |
|
| Effects of 4-ethylamino-2-butynyl(2-cyclohexyl-2-phenyl)glycolate hydrochloride, a metabolite of oxybutynin, on bladder specimens and rhythmic bladder contraction in rats in comparison with oxybutynin. | 2004-02 |
Patents
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Preferred Name | English | ||
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Code | English |
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80976-67-6
Created by
admin on Mon Mar 31 21:41:45 GMT 2025 , Edited by admin on Mon Mar 31 21:41:45 GMT 2025
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DTXSID701001668
Created by
admin on Mon Mar 31 21:41:45 GMT 2025 , Edited by admin on Mon Mar 31 21:41:45 GMT 2025
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8809SNK4F7
Created by
admin on Mon Mar 31 21:41:45 GMT 2025 , Edited by admin on Mon Mar 31 21:41:45 GMT 2025
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133577
Created by
admin on Mon Mar 31 21:41:45 GMT 2025 , Edited by admin on Mon Mar 31 21:41:45 GMT 2025
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PRIMARY |
PARENT (METABOLITE ACTIVE)
SALT/SOLVATE (PARENT)
SUBSTANCE RECORD
