Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H24N2O3 |
| Molecular Weight | 304.3841 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(=O)N(C1=CC=CC=C1)C2(CCN(C)CC2)C(=O)OC
InChI
InChIKey=KKEVIELPQLXPRR-UHFFFAOYSA-N
InChI=1S/C17H24N2O3/c1-4-15(20)19(14-8-6-5-7-9-14)17(16(21)22-3)10-12-18(2)13-11-17/h5-9H,4,10-13H2,1-3H3
Approval Year
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WIKIPEDIA |
List_of_fentanyl_analogues
Created by
admin on Sat Dec 16 10:30:19 GMT 2023 , Edited by admin on Sat Dec 16 10:30:19 GMT 2023
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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85WEL251JZ
Created by
admin on Sat Dec 16 10:30:19 GMT 2023 , Edited by admin on Sat Dec 16 10:30:19 GMT 2023
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PRIMARY | |||
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12298013
Created by
admin on Sat Dec 16 10:30:19 GMT 2023 , Edited by admin on Sat Dec 16 10:30:19 GMT 2023
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PRIMARY | |||
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59708-50-8
Created by
admin on Sat Dec 16 10:30:19 GMT 2023 , Edited by admin on Sat Dec 16 10:30:19 GMT 2023
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PRIMARY | |||
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N-METHYLCARFENTANIL
Created by
admin on Sat Dec 16 10:30:19 GMT 2023 , Edited by admin on Sat Dec 16 10:30:19 GMT 2023
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PRIMARY | |||
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N-Methylnorcarfentanil
Created by
admin on Sat Dec 16 10:30:19 GMT 2023 , Edited by admin on Sat Dec 16 10:30:19 GMT 2023
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PRIMARY | N-Methylnorcarfentanil (R-32395) is an opioid analgesic drug related to the highly potent animal tranquilizer carfentanil, but several thousand times weaker, being only slightly stronger than morphine. It was first synthesised by a team of chemists at Janssen Pharmaceutica led by Paul Janssen, who were investigating the structure-activity relationships of the fentanyl family of drugs. They found that replacing the phenethyl group attached to the piperidine nitrogen of fentanyl with a smaller methyl group, made it so much weaker that it was inactive as an analgesic in animals. However the same change made to the more potent analogue carfentanil retained reasonable opioid receptor activity, reflecting the higher binding affinity produced by the 4-carbomethoxy group. | ||
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DTXSID501029751
Created by
admin on Sat Dec 16 10:30:19 GMT 2023 , Edited by admin on Sat Dec 16 10:30:19 GMT 2023
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PRIMARY |
ACTIVE MOIETY
