Details
| Stereochemistry | UNKNOWN |
| Molecular Formula | C12H23N.BrH |
| Molecular Weight | 262.23 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 0 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Br.CN(C)C1(C)C2CCC(C2)C1(C)C
InChI
InChIKey=JLCYKWACZFDYOT-UHFFFAOYSA-N
InChI=1S/C12H23N.BrH/c1-11(2)9-6-7-10(8-9)12(11,3)13(4)5;/h9-10H,6-8H2,1-5H3;1H
| Molecular Formula | C12H23N |
| Molecular Weight | 181.3177 |
| Charge | 0 |
| Count |
|
| Stereochemistry | MIXED |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
| Molecular Formula | BrH |
| Molecular Weight | 80.912 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Dimecamine is ganglion blocking agent. A slowly developing but moderate contracture of the chick biventer cervicis muscle was observed with 5x10-4M-dimecamine methiodide solution. A small reduction in the twitch response was also observed. Similar concentrations of dimecamine and pempidine produced only slowly developing and very small contractures. Dimecamine differs in neuromuscular-blocking activity from its corresponding quaternary metho-salts by a factor of less than two.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:46:38 GMT 2025
by
admin
on
Mon Mar 31 22:46:38 GMT 2025
|
| Record UNII |
O2I9591ZTO
|
| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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Systematic Name | English |
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201651
Created by
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DTXSID30983357
Created by
admin on Mon Mar 31 22:46:38 GMT 2025 , Edited by admin on Mon Mar 31 22:46:38 GMT 2025
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6472-63-5
Created by
admin on Mon Mar 31 22:46:38 GMT 2025 , Edited by admin on Mon Mar 31 22:46:38 GMT 2025
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PRIMARY | |||
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O2I9591ZTO
Created by
admin on Mon Mar 31 22:46:38 GMT 2025 , Edited by admin on Mon Mar 31 22:46:38 GMT 2025
|
PRIMARY |
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