Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C12H16N2O |
| Molecular Weight | 204.2682 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C2NC=C(CC(C)N)C2=C1
InChI
InChIKey=OGNJZVNNKBZFRM-UHFFFAOYSA-N
InChI=1S/C12H16N2O/c1-8(13)5-9-7-14-12-4-3-10(15-2)6-11(9)12/h3-4,6-8,14H,5,13H2,1-2H3
| Molecular Formula | C12H16N2O |
| Molecular Weight | 204.2682 |
| 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: P08908 Gene ID: 3350.0 Gene Symbol: HTR1A Target Organism: Homo sapiens (Human) |
46.0 nM [Ki] | ||
Target ID: P28223 Gene ID: 3356.0 Gene Symbol: HTR2A Target Organism: Homo sapiens (Human) |
2.0 nM [EC50] | ||
Target ID: P41595 Gene ID: 3357.0 Gene Symbol: HTR2B Target Organism: Homo sapiens (Human) |
4.0 nM [EC50] |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:51:50 UTC 2023
by
admin
on
Sat Dec 16 09:51:50 UTC 2023
|
| Record UNII |
U5XOB9AQ15
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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WIKIPEDIA |
TiHKAL
Created by
admin on Sat Dec 16 09:51:50 UTC 2023 , Edited by admin on Sat Dec 16 09:51:50 UTC 2023
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WIKIPEDIA |
Designer-drugs-5-MeO-aMT
Created by
admin on Sat Dec 16 09:51:50 UTC 2023 , Edited by admin on Sat Dec 16 09:51:50 UTC 2023
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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5-MEO-AMT
Created by
admin on Sat Dec 16 09:51:50 UTC 2023 , Edited by admin on Sat Dec 16 09:51:50 UTC 2023
|
PRIMARY | 5-MeO-aMT or 5-methoxy-α-methyltryptamine, α,O-Dimethylserotonin (Alpha-O) is a potent psychedelic tryptamine. It is soluble in ethanol. The sympathomimetic effects may in turn be caused by 5-MeO-AMT's structural similarity to the amphetamines. As noted by Alexander Shulgin, the alpha-methylated tryptamines can be looked at as the tryptamine homologues of the amphetamines (alpha-methylated phenethylamines). Mechanisms of action such as inhibition of monoamine reuptake may be involved also. | ||
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DTXSID60893758
Created by
admin on Sat Dec 16 09:51:50 UTC 2023 , Edited by admin on Sat Dec 16 09:51:50 UTC 2023
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PRIMARY | |||
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1137-04-8
Created by
admin on Sat Dec 16 09:51:50 UTC 2023 , Edited by admin on Sat Dec 16 09:51:50 UTC 2023
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PRIMARY | |||
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36906
Created by
admin on Sat Dec 16 09:51:50 UTC 2023 , Edited by admin on Sat Dec 16 09:51:50 UTC 2023
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PRIMARY | |||
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U5XOB9AQ15
Created by
admin on Sat Dec 16 09:51:50 UTC 2023 , Edited by admin on Sat Dec 16 09:51:50 UTC 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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TARGET -> AGONIST |
Ki
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TARGET -> AGONIST |
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TARGET -> AGONIST |
Ki
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ACTIVE MOIETY |
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