Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C21H24N2O4 |
| Molecular Weight | 368.4263 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C(NC1=CC=CC=C1)OCC3(COC(=O)NC2=CC=CC=C2)CCCC3
InChI
InChIKey=IRZVVDMCEZNNCW-UHFFFAOYSA-N
InChI=1S/C21H24N2O4/c24-19(22-17-9-3-1-4-10-17)26-15-21(13-7-8-14-21)16-27-20(25)23-18-11-5-2-6-12-18/h1-6,9-12H,7-8,13-16H2,(H,22,24)(H,23,25)
| Molecular Formula | C21H24N2O4 |
| Molecular Weight | 368.4263 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Cyclarbamate (N,N-diphenyl dicarbamate of 1,1-cyclopentanedimethanol) possesses an action on the central nervous system which manifests itself by a sedative effect without abolition of the natural defense reflexes. It is also antispasmodics of the striated muscle fibre. It has been studied in gastroenterology and gynecology.
CNS Activity
Originator
Sources: https://patents.google.com/patent/US3067240
Curator's Comment: reference retrieved from: https://books.google.ru/books?id=_J2ti4EkYpkC&printsec=frontcover&hl=ru#v=onepage&q&f=false
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:57:09 GMT 2025
by
admin
on
Wed Apr 02 09:57:09 GMT 2025
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| Record UNII |
779291866J
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| Record Status |
Validated (UNII)
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| Record Version |
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Official Name | English | ||
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Preferred Name | English | ||
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C264
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admin on Wed Apr 02 09:57:09 GMT 2025 , Edited by admin on Wed Apr 02 09:57:09 GMT 2025
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227-302-7
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DTXSID60206480
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3722
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1389
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m134
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779291866J
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C77248
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100000083746
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C004637
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5779-54-4
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SUB06842MIG
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Cyclarbamate
Created by
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72076
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CHEMBL2104142
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |