Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C26H34N2O |
| Molecular Weight | 390.561 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1CCCCC1CN2C=C(C(=O)C34CC5CC(CC(C5)C3)C4)C6=C2C=CC=C6
InChI
InChIKey=JRECAXBHMULNJQ-UHFFFAOYSA-N
InChI=1S/C26H34N2O/c1-27-9-5-4-6-21(27)16-28-17-23(22-7-2-3-8-24(22)28)25(29)26-13-18-10-19(14-26)12-20(11-18)15-26/h2-3,7-8,17-21H,4-6,9-16H2,1H3
| Molecular Formula | C26H34N2O |
| Molecular Weight | 390.561 |
| 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: P21554|||Q5UB37 Gene ID: 1268.0 Gene Symbol: CNR1 Target Organism: Homo sapiens (Human) Sources: https://patents.google.com/patent/US7820144 |
11.93 nM [Ki] | ||
Target ID: P34972 Gene ID: 1269.0 Gene Symbol: CNR2 Target Organism: Homo sapiens (Human) Sources: https://patents.google.com/patent/US7820144 |
4.804 nM [Ki] |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:23:13 GMT 2025
by
admin
on
Mon Mar 31 23:23:13 GMT 2025
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| Record UNII |
5EX9HEF4HK
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| Record Status |
Validated (UNII)
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| Record Version |
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WIKIPEDIA |
Designer-drugs-AM-1248
Created by
admin on Mon Mar 31 23:23:13 GMT 2025 , Edited by admin on Mon Mar 31 23:23:13 GMT 2025
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10293794
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DTXSID101017326
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335160-66-2
Created by
admin on Mon Mar 31 23:23:13 GMT 2025 , Edited by admin on Mon Mar 31 23:23:13 GMT 2025
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5EX9HEF4HK
Created by
admin on Mon Mar 31 23:23:13 GMT 2025 , Edited by admin on Mon Mar 31 23:23:13 GMT 2025
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AM-1248
Created by
admin on Mon Mar 31 23:23:13 GMT 2025 , Edited by admin on Mon Mar 31 23:23:13 GMT 2025
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PRIMARY |
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