Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C23H26N2O2 |
| Molecular Weight | 362.4647 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1CC[C@@](C2CCN(CC3=CC=CC=C3)CC2)(C(=O)N1)C4=CC=CC=C4
InChI
InChIKey=LQQIVYSCPWCSSD-HSZRJFAPSA-N
InChI=1S/C23H26N2O2/c26-21-11-14-23(22(27)24-21,19-9-5-2-6-10-19)20-12-15-25(16-13-20)17-18-7-3-1-4-8-18/h1-10,20H,11-17H2,(H,24,26,27)/t23-/m1/s1
| Molecular Formula | C23H26N2O2 |
| Molecular Weight | 362.4647 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Dexetimide is a potent central and peripheral anticholinergic agent. It has a high affinity for all subtypes of muscarinic receptor and a long duration action. It forms very stable complex with mAChR. Dexetimide was used for many years in Europe for the treatment of extrapyramidal disorders. Neuroleptic-induced parkinsonian symptoms are effectively controlled by dexetimide. It is a safe, potent, and long-acting antiparkinsonian agent.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Pharmacological comparison of the cloned human and rat M2 muscarinic receptor genes expressed in the murine fibroblast (B82) cell line. | 1998-02 |
|
| Subclassification of muscarinic receptors in the heart, urinary bladder and sympathetic ganglia in the pithed rat. Selectivity of some classical agonists. | 1985-12 |
|
| Dexetimide (R 16470) in the control of neuroleptic-induced extrapyramidal side-effects. Its prophylactic value and duration of action. | 1973-07-01 |
|
| A quantitative study of neuroleptic-induced extrapyramidal symptoms and their response to dexetimide, a potent and long-acting antiparkinsonian agent. | 1971 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1020682
Dosages ranged from 0.5 to 1.5 mg daily
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:19:32 GMT 2025
by
admin
on
Mon Mar 31 18:19:32 GMT 2025
|
| Record UNII |
43477QYX3D
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
WHO-VATC |
QN04AA08
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
||
|
NCI_THESAURUS |
C29704
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
||
|
WHO-ATC |
N04AA08
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
D003909
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
CHEMBL1908364
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
354
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
DB08997
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
SUB07026MIG
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
30843
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
3267
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | RxNorm | ||
|
DTXSID701043218
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
831
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
m4217
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | Merck Index | ||
|
2726
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
100000083202
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
21888-98-2
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
43477QYX3D
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
C78069
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
Dexetimide
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
SALT/SOLVATE -> PARENT | |||
|
|
RACEMATE -> ENANTIOMER |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |