Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C26H29NO4 |
| Molecular Weight | 419.5128 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=C(OC2=C(C=CC=C2C(=O)OC(C)(C)CN3CCCCC3)C1=O)C4=CC=CC=C4
InChI
InChIKey=VQTYZZPDAFGNCK-UHFFFAOYSA-N
InChI=1S/C26H29NO4/c1-18-22(28)20-13-10-14-21(24(20)30-23(18)19-11-6-4-7-12-19)25(29)31-26(2,3)17-27-15-8-5-9-16-27/h4,6-7,10-14H,5,8-9,15-17H2,1-3H3
| Molecular Formula | C26H29NO4 |
| Molecular Weight | 419.5128 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Terflavoxate is a benzopyran derivative patented by Recordati S. A. Chemical and Pharmaceutical Co. as a muscle relaxant, anesthetic, anti-inflammatory, and antispastic agent useful for the treatment of lower urinary tract disease. Terflavoxate inhibited by more than 50% field stimulation-induced contractions of rabbit bladder strips, indicates that mechanisms other than the anticholinergic one should be responsible for its smooth muscle relaxant properties.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:10:48 GMT 2025
by
admin
on
Mon Mar 31 18:10:48 GMT 2025
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| Record UNII |
NKF031O02G
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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Official Name | English |
| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29698
Created by
admin on Mon Mar 31 18:10:48 GMT 2025 , Edited by admin on Mon Mar 31 18:10:48 GMT 2025
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| Code System | Code | Type | Description | ||
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6466
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86433-40-1
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NKF031O02G
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DTXSID90235541
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C059474
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CHEMBL2106728
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C76466
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100000082689
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SUB10921MIG
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135750
Created by
admin on Mon Mar 31 18:10:48 GMT 2025 , Edited by admin on Mon Mar 31 18:10:48 GMT 2025
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |