Details
Stereochemistry | RACEMIC |
Molecular Formula | C21H23N.ClH |
Molecular Weight | 325.875 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.[H][C@@]12CCCCN1C[C@@]3([H])C4=C(CCC5=CC=CC2=C35)C=CC=C4
InChI
InChIKey=LOSFVNFVCCXCEN-FKLPMGAJSA-N
InChI=1S/C21H23N.ClH/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;1H/t19-,20-;/m0./s1
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 | C21H23N |
Molecular Weight | 289.414 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
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
Fri Dec 15 15:02:45 GMT 2023
by
admin
on
Fri Dec 15 15:02:45 GMT 2023
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Record UNII |
0R94K6TJ5B
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C78272
Created by
admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
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Code System | Code | Type | Description | ||
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C152487
Created by
admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
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PRIMARY | |||
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0R94K6TJ5B
Created by
admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
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CHEMBL2111072
Created by
admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
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DTXSID70955619
Created by
admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
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PRIMARY | |||
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C010342
Created by
admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
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PRIMARY | |||
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76968505
Created by
admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
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34061-34-2
Created by
admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |