Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C19H27N3O |
| Molecular Weight | 313.4372 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCN1C=C(C(=O)N2CCN(C)CC2)C3=C1C=CC=C3
InChI
InChIKey=IUEFFEOHJKCBPF-UHFFFAOYSA-N
InChI=1S/C19H27N3O/c1-3-4-7-10-22-15-17(16-8-5-6-9-18(16)22)19(23)21-13-11-20(2)12-14-21/h5-6,8-9,15H,3-4,7,10-14H2,1-2H3
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2096981 Sources: https://www.ncbi.nlm.nih.gov/pubmed/29367864 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Postmortem distribution of mepirapim and acetyl fentanyl in biological fluid and solid tissue specimens measured by the standard addition method. | 2019 |
|
| Identification and quantification of mepirapim and acetyl fentanyl in authentic human whole blood and urine samples by GC-MS/MS and LC-MS/MS. | 2018 |
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Preferred Name | English | ||
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Common Name | English |
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WIKIPEDIA |
Designer-drugs-MEPIRAPIM
Created by
admin on Mon Mar 31 23:10:34 GMT 2025 , Edited by admin on Mon Mar 31 23:10:34 GMT 2025
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| Code System | Code | Type | Description | ||
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W6OZW1T05K
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101896603
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2365542-29-4
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admin on Mon Mar 31 23:10:34 GMT 2025 , Edited by admin on Mon Mar 31 23:10:34 GMT 2025
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MEPIRAPIM
Created by
admin on Mon Mar 31 23:10:34 GMT 2025 , Edited by admin on Mon Mar 31 23:10:34 GMT 2025
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PRIMARY | MEPIRAPIM is a indole-based cannabinoid which differs from JWH-018 by having a 4-methylpiperazine group in place of the naphthyl group(1) and has been used as an active ingredient in synthetic cannabis products. It was first identified in Japan in 2013, alongside FUBIMINA. | ||
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MEPIRAPIM
Created by
admin on Mon Mar 31 23:10:34 GMT 2025 , Edited by admin on Mon Mar 31 23:10:34 GMT 2025
|
PRIMARY | MEPIRAPIM is a indole-based cannabinoid which differs from JWH-018 by having a 4-methylpiperazine group in place of the naphthyl group(1) and has been used as an active ingredient in synthetic cannabis products. It was first identified in Japan in 2013, alongside FUBIMINA. Sweden's public health agency suggested to classify MEPIRAPIM as hazardous substance on November 10, 2014. |
ACTIVE MOIETY