Details
Stereochemistry | RACEMIC |
Molecular Formula | C23H34N3O3.I |
Molecular Weight | 527.4388 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[I-].CC[N@+]1(C)CC[C@@H](CC1)OC(=O)[C@H](N2CCCCCC2)C3=NOC4=CC=CC=C34
InChI
InChIKey=XEHKKWZHSSPBNZ-AQAMNGIHSA-M
InChI=1S/C23H34N3O3.HI/c1-3-26(2)16-12-18(13-17-26)28-23(27)22(25-14-8-4-5-9-15-25)21-19-10-6-7-11-20(19)29-24-21;/h6-7,10-11,18,22H,3-5,8-9,12-17H2,1-2H3;1H/q+1;/p-1/t18-,22-,26+;/m1./s1
Molecular Formula | HI |
Molecular Weight | 127.9124 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C23H34N3O3 |
Molecular Weight | 400.5344 |
Charge | 1 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/3741526
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3741526
Beperidium (also known as SX-810 ) is a competitive antagonist against acetylcholine. Experiments on animal have shown that this compound exhibited spasmolytic and antiulcerative activities without exerting systemic antimuscarinic side effects.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:30:00 GMT 2023
by
admin
on
Fri Dec 15 15:30:00 GMT 2023
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Record UNII |
25OIG0XCVX
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Record Status |
Validated (UNII)
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Record Version |
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-
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Official Name | English | ||
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Code | English |
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NCI_THESAURUS |
C66880
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DTXSID001006843
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C72590
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SUB05775MIG
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6121
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100000086047
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86434-57-3
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25OIG0XCVX
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CHEMBL2110605
Created by
admin on Fri Dec 15 15:30:00 GMT 2023 , Edited by admin on Fri Dec 15 15:30:00 GMT 2023
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Related Record | Type | Details | ||
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ACTIVE MOIETY |