Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C21H23N |
| Molecular Weight | 289.414 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C1CCN2C[C@H]3C4=C(CCC5=CC=CC([C@@H]2C1)=C35)C=CC=C4
InChI
InChIKey=BFHGFZIDLRXFJE-PMACEKPBSA-N
InChI=1S/C21H23N/c1-2-8-17-15(6-1)11-12-16-7-5-9-18-20-10-3-4-13-22(20)14-19(17)21(16)18/h1-2,5-9,19-20H,3-4,10-14H2/t19-,20-/m0/s1
| Molecular Formula | C21H23N |
| Molecular Weight | 289.414 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Taclamine is an isoquinoline derivative patented by Ayerst, McKenna and Harrison Ltd. as central nervous system depressant and anti-inflammatory agent. In preclinical models, Taclamine antagonizes the turnover of noradrenaline and dopamine in the rat brain during immobilization stress without effects on brain serotonin turnover
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:12:45 GMT 2025
by
admin
on
Mon Mar 31 19:12:45 GMT 2025
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| Record UNII |
P98BJE9F79
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| Record Status |
Validated (UNII)
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| Record Version |
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| Name | Type | Language | ||
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Official Name | English | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C78272
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admin on Mon Mar 31 19:12:45 GMT 2025 , Edited by admin on Mon Mar 31 19:12:45 GMT 2025
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| Code System | Code | Type | Description | ||
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CHEMBL2111072
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DTXSID901043357
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SUB10795MIG
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C152486
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P98BJE9F79
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76968506
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100000083013
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3274
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34061-33-1
Created by
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PRIMARY |
| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |