Details
Stereochemistry | RACEMIC |
Molecular Formula | C20H27NO2 |
Molecular Weight | 313.4339 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(OC)C=C(C=C1)C(CCCC2=CC=CC=C2)N(C)C
InChI
InChIKey=HEFVRVOEBZDOJU-UHFFFAOYSA-N
InChI=1S/C20H27NO2/c1-21(2)18(12-8-11-16-9-6-5-7-10-16)17-13-14-19(22-3)20(15-17)23-4/h5-7,9-10,13-15,18H,8,11-12H2,1-4H3
Molecular Formula | C20H27NO2 |
Molecular Weight | 313.4339 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Vetrabutine is a spasmolytic agent. As a musculotropic spasmolytic agent vatrabutine was reported to act directly on the smooth muscle fibers and to have no neurotropic activity. In pigs, its activity was specific to the uterine body and cervical musculature where it acted on the myometrial cells, sealing off the membrane against the passage of potassium ions, thereby increasing membrane potential and lowering tonus. Vetrabutine was of moderate acute oral toxicity. Vetributine hydrochloride has been used in human medicine as a spasmolytic agent in obstetrics.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:53:46 GMT 2023
by
admin
on
Sat Dec 16 17:53:46 GMT 2023
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Record UNII |
I3E2J32F37
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29698
Created by
admin on Sat Dec 16 17:53:46 GMT 2023 , Edited by admin on Sat Dec 16 17:53:46 GMT 2023
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WHO-VATC |
QG02CA90
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admin on Sat Dec 16 17:53:46 GMT 2023 , Edited by admin on Sat Dec 16 17:53:46 GMT 2023
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Code System | Code | Type | Description | ||
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I3E2J32F37
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4010
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SUB00046MIG
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m11438
Created by
admin on Sat Dec 16 17:53:46 GMT 2023 , Edited by admin on Sat Dec 16 17:53:46 GMT 2023
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PRIMARY | Merck Index | ||
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C73164
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100000079083
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admin on Sat Dec 16 17:53:46 GMT 2023 , Edited by admin on Sat Dec 16 17:53:46 GMT 2023
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CHEMBL2104458
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DTXSID90863262
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3735-45-3
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admin on Sat Dec 16 17:53:46 GMT 2023 , Edited by admin on Sat Dec 16 17:53:46 GMT 2023
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111122
Created by
admin on Sat Dec 16 17:53:46 GMT 2023 , Edited by admin on Sat Dec 16 17:53:46 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE | |||
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SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
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ACTIVE MOIETY |