Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C15H20N2O |
| Molecular Weight | 244.3321 |
| Optical Activity | ( + ) |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC2=C(NC=C2C[C@H]3CCCN3C)C=C1
InChI
InChIKey=MKEGUJPBCIXABO-GFCCVEGCSA-N
InChI=1S/C15H20N2O/c1-17-7-3-4-12(17)8-11-10-16-15-6-5-13(18-2)9-14(11)15/h5-6,9-10,12,16H,3-4,7-8H2,1-2H3/t12-/m1/s1
| Molecular Formula | C15H20N2O |
| Molecular Weight | 244.3321 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:08:23 GMT 2025
by
admin
on
Mon Mar 31 23:08:23 GMT 2025
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| Record UNII |
N29TFW7VRV
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| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
| Name | Type | Language | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Common Name | English |
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WIKIPEDIA |
Designer-drugs-5-MeO-MPMI
Created by
admin on Mon Mar 31 23:08:23 GMT 2025 , Edited by admin on Mon Mar 31 23:08:23 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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5-MEO-MPMI
Created by
admin on Mon Mar 31 23:08:23 GMT 2025 , Edited by admin on Mon Mar 31 23:08:23 GMT 2025
|
PRIMARY | 5-MeO-MPMI (also known as 5-Methoxy-N-methyl-(α,N-trimethylene)tryptamine) is a tryptamine derivative that is a psychedelic drug. It was first developed by the team led by JE Macor in 1992,[1] and subsequently investigated by the team led by David Nichols from Purdue University in the late 1990s. This compound produces psychedelic-appropriate responding in animal tests with a similar potency to the amphetamine-derived psychedelic DOI, and has two enantiomers, with only the (R)-enantiomer being active. | ||
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143321-57-7
Created by
admin on Mon Mar 31 23:08:23 GMT 2025 , Edited by admin on Mon Mar 31 23:08:23 GMT 2025
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9881324
Created by
admin on Mon Mar 31 23:08:23 GMT 2025 , Edited by admin on Mon Mar 31 23:08:23 GMT 2025
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N29TFW7VRV
Created by
admin on Mon Mar 31 23:08:23 GMT 2025 , Edited by admin on Mon Mar 31 23:08:23 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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TARGET -> AGONIST |
Ki
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ACTIVE MOIETY |
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