Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C22H27FN2O2 |
| Molecular Weight | 370.4604 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COCC(=O)N(C1CCN(CCC2=CC=CC=C2)CC1)C3=C(F)C=CC=C3
InChI
InChIKey=NYISTOZKVCMVEL-UHFFFAOYSA-N
InChI=1S/C22H27FN2O2/c1-27-17-22(26)25(21-10-6-5-9-20(21)23)19-12-15-24(16-13-19)14-11-18-7-3-2-4-8-18/h2-10,19H,11-17H2,1H3
| Molecular Formula | C22H27FN2O2 |
| Molecular Weight | 370.4604 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:44:02 UTC 2023
by
admin
on
Fri Dec 15 16:44:02 UTC 2023
|
| Record UNII |
MX52WBC8EV
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
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Official Name | English | ||
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Systematic 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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Common Name | English | ||
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Code | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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DEA NO. |
9838
Created by
admin on Fri Dec 15 16:44:02 UTC 2023 , Edited by admin on Fri Dec 15 16:44:02 UTC 2023
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WIKIPEDIA |
List_of_fentanyl_analogues
Created by
admin on Fri Dec 15 16:44:02 UTC 2023 , Edited by admin on Fri Dec 15 16:44:02 UTC 2023
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NCI_THESAURUS |
C67413
Created by
admin on Fri Dec 15 16:44:02 UTC 2023 , Edited by admin on Fri Dec 15 16:44:02 UTC 2023
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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101343-69-5
Created by
admin on Fri Dec 15 16:44:02 UTC 2023 , Edited by admin on Fri Dec 15 16:44:02 UTC 2023
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PRIMARY | |||
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C84024
Created by
admin on Fri Dec 15 16:44:02 UTC 2023 , Edited by admin on Fri Dec 15 16:44:02 UTC 2023
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PRIMARY | |||
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60575
Created by
admin on Fri Dec 15 16:44:02 UTC 2023 , Edited by admin on Fri Dec 15 16:44:02 UTC 2023
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PRIMARY | |||
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100000083857
Created by
admin on Fri Dec 15 16:44:02 UTC 2023 , Edited by admin on Fri Dec 15 16:44:02 UTC 2023
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PRIMARY | |||
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OCFENTANIL
Created by
admin on Fri Dec 15 16:44:02 UTC 2023 , Edited by admin on Fri Dec 15 16:44:02 UTC 2023
|
PRIMARY | In human volunteers ocfentanil induces effective analgesia at 1 .MU.g/kg, while in doses up to 3 .MU.g/kg, analgesia and respiratory depression occurred in a dose-dependent manner. While a further study suggests that ocfentanil may be as effective as morphine in post-operative relief,(4) Ocfentanil was also studied as a supplement to general anaesthesia, in which the researchers concluded that it appears to be similar in action to fentanyl, with 3 .MU.g/kg of ocfentanil approximately equivalent to 5 .MU.g/kg of fentanyl. | ||
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DTXSID00869356
Created by
admin on Fri Dec 15 16:44:02 UTC 2023 , Edited by admin on Fri Dec 15 16:44:02 UTC 2023
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PRIMARY | |||
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MX52WBC8EV
Created by
admin on Fri Dec 15 16:44:02 UTC 2023 , Edited by admin on Fri Dec 15 16:44:02 UTC 2023
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PRIMARY | |||
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C071395
Created by
admin on Fri Dec 15 16:44:02 UTC 2023 , Edited by admin on Fri Dec 15 16:44:02 UTC 2023
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PRIMARY | |||
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SUB09396MIG
Created by
admin on Fri Dec 15 16:44:02 UTC 2023 , Edited by admin on Fri Dec 15 16:44:02 UTC 2023
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PRIMARY | |||
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CHEMBL2110917
Created by
admin on Fri Dec 15 16:44:02 UTC 2023 , Edited by admin on Fri Dec 15 16:44:02 UTC 2023
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PRIMARY | |||
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6448
Created by
admin on Fri Dec 15 16:44:02 UTC 2023 , Edited by admin on Fri Dec 15 16:44:02 UTC 2023
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PRIMARY | |||
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OCFENTANIL
Created by
admin on Fri Dec 15 16:44:02 UTC 2023 , Edited by admin on Fri Dec 15 16:44:02 UTC 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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TARGET -> AGONIST | |||
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SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
