Details
Stereochemistry | RACEMIC |
Molecular Formula | C11H14N2 |
Molecular Weight | 174.2423 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(N)CC1=CC2=C(C=CN2)C=C1
InChI
InChIKey=QCFIFKAOUKPFPU-UHFFFAOYSA-N
InChI=1S/C11H14N2/c1-8(12)6-9-2-3-10-4-5-13-11(10)7-9/h2-5,7-8,13H,6,12H2,1H3
Molecular Formula | C11H14N2 |
Molecular Weight | 174.2423 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: GO:0097621 Sources: https://www.ncbi.nlm.nih.gov/pubmed/5658327 |
4.6 µM [IC50] |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:01:33 GMT 2023
by
admin
on
Sat Dec 16 11:01:33 GMT 2023
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Record UNII |
27230C15B7
|
Record Status |
Validated (UNII)
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Record Version |
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-
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30999
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DTXSID501030112
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admin on Sat Dec 16 11:01:33 GMT 2023 , Edited by admin on Sat Dec 16 11:01:33 GMT 2023
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6-(2-Aminopropyl)indole
Created by
admin on Sat Dec 16 11:01:33 GMT 2023 , Edited by admin on Sat Dec 16 11:01:33 GMT 2023
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21005-63-0
Created by
admin on Sat Dec 16 11:01:33 GMT 2023 , Edited by admin on Sat Dec 16 11:01:33 GMT 2023
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27230C15B7
Created by
admin on Sat Dec 16 11:01:33 GMT 2023 , Edited by admin on Sat Dec 16 11:01:33 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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SALT/SOLVATE -> PARENT | |||
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ENANTIOMER -> RACEMATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |
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