Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C23H26N2O2.ClH |
| Molecular Weight | 398.926 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.O=C1CCC(C2CCN(CC3=CC=CC=C3)CC2)(C(=O)N1)C4=CC=CC=C4
InChI
InChIKey=XSOOSXRNMDUWEM-UHFFFAOYSA-N
InChI=1S/C23H26N2O2.ClH/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);1H
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C23H26N2O2 |
| Molecular Weight | 362.4647 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis and structure-activity relationship of benzetimide derivatives as human CXCR3 antagonists. | 2008-11-01 |
|
| Reduced posterior cingulate binding of I-123 iodo-dexetimide to muscarinic receptors in mild Alzheimer's disease. | 2005-05 |
|
| Defects in muscarinic receptor-coupled signal transduction in isolated parotid gland cells after in vivo irradiation: evidence for a non-DNA target of radiation. | 2005-02-14 |
|
| Sequential 123I-iododexetimide scans in temporal lobe epilepsy: comparison with neuroimaging scans (MR imaging and 18F-FDG PET imaging). | 2005-02 |
|
| Variable effects of previously untested muscarinic receptor antagonists on experimental myopia. | 2003-03 |
|
| Labelling of the solvent DMSO as side reaction of methylations with n.c.a. [11C]CH3I. | 2001-09 |
|
| The allosteric interaction of otenzepad (AF-DX 116) at muscarinic M2 receptors in guinea pig atria. | 2001-03-30 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:49:03 GMT 2025
by
admin
on
Mon Mar 31 18:49:03 GMT 2025
|
| Record UNII |
V6ERX20PHB
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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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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29704
Created by
admin on Mon Mar 31 18:49:03 GMT 2025 , Edited by admin on Mon Mar 31 18:49:03 GMT 2025
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| Code System | Code | Type | Description | ||
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300000029154
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PRIMARY | |||
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CHEMBL10272
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5633-14-7
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DTXSID101036320
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21846
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227-072-8
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m2347
Created by
admin on Mon Mar 31 18:49:03 GMT 2025 , Edited by admin on Mon Mar 31 18:49:03 GMT 2025
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PRIMARY | Merck Index | ||
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C78062
Created by
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V6ERX20PHB
Created by
admin on Mon Mar 31 18:49:03 GMT 2025 , Edited by admin on Mon Mar 31 18:49:03 GMT 2025
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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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PARENT -> SALT/SOLVATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |