Details
Stereochemistry | RACEMIC |
Molecular Formula | C13H18N2 |
Molecular Weight | 202.2954 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(N)CC1=CNC2=C(C)C=CC=C12
InChI
InChIKey=NBLFITFQOPGXLS-UHFFFAOYSA-N
InChI=1S/C13H18N2/c1-3-11(14)7-10-8-15-13-9(2)5-4-6-12(10)13/h4-6,8,11,15H,3,7,14H2,1-2H3
Molecular Formula | C13H18N2 |
Molecular Weight | 202.2954 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:19:12 GMT 2023
by
admin
on
Sat Dec 16 17:19:12 GMT 2023
|
Record UNII |
7H5EU45L83
|
Record Status |
Validated (UNII)
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Record Version |
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-
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Common Name | English |
Code System | Code | Type | Description | ||
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7H5EU45L83
Created by
admin on Sat Dec 16 17:19:12 GMT 2023 , Edited by admin on Sat Dec 16 17:19:12 GMT 2023
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57469234
Created by
admin on Sat Dec 16 17:19:12 GMT 2023 , Edited by admin on Sat Dec 16 17:19:12 GMT 2023
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13712-80-6
Created by
admin on Sat Dec 16 17:19:12 GMT 2023 , Edited by admin on Sat Dec 16 17:19:12 GMT 2023
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7-Methyl-α-ethyltryptamine
Created by
admin on Sat Dec 16 17:19:12 GMT 2023 , Edited by admin on Sat Dec 16 17:19:12 GMT 2023
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DTXSID60726754
Created by
admin on Sat Dec 16 17:19:12 GMT 2023 , Edited by admin on Sat Dec 16 17:19:12 GMT 2023
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Related Record | Type | Details | ||
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TARGET -> INHIBITOR |
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PARENT -> DERIVATIVE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |
3-4 times more potent as a serotonin releasing agent, and 10 times more potent as a monoamine oxidase inhibitor.
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