Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C25H33NO4.ClH |
Molecular Weight | 447.995 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 7 / 7 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCC[C@@](C)(O)[C@H]1C[C@@]23C=C[C@]1(OC)[C@@H]4OC5=C(O)C=CC6=C5[C@]24CCN(C)[C@@H]3C6
InChI
InChIKey=JNHPUZURWFYYHW-DTUSRQQPSA-N
InChI=1S/C25H33NO4.ClH/c1-5-8-22(2,28)17-14-23-9-10-25(17,29-4)21-24(23)11-12-26(3)18(23)13-15-6-7-16(27)20(30-21)19(15)24;/h6-7,9-10,17-18,21,27-28H,5,8,11-14H2,1-4H3;1H/t17-,18-,21-,22-,23-,24+,25-;/m1./s1
Molecular Formula | C25H33NO4 |
Molecular Weight | 411.5338 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 7 / 7 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Etorphine was the first potent opiate agonist employed primarily for use in non-domestic and wild species. Etorphine was 500 times as potent as morphine, with a very rapid onset and short duration of action. In morphine-dependent subjects, etorphine suppressed abstinence but for a shorter period than morphine. Etorphine is a full opiate agonist and binds to multiple opiate sites in the central nervous system. It is believed to produce its clinical effects through binding the µ-, δ-, and κ- opiate sites. It has a potent effect on depressing the respiratory centers of the CNS thus resulting in apnea being commonly seen in immobilized animals. Etorphine revolutionized the ability of biologists and veterinarians to safely capture and restrain many species that previously could not be handled. Etorphine is not currently commercially available due to lack of production by the manufacturer.
CNS Activity
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:02:38 GMT 2025
by
admin
on
Mon Mar 31 18:02:38 GMT 2025
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Record UNII |
8CBE01N748
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Record Status |
Validated (UNII)
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Record Version |
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-
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Common Name | English | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Code | English | ||
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Common Name | English |
Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C67413
Created by
admin on Mon Mar 31 18:02:38 GMT 2025 , Edited by admin on Mon Mar 31 18:02:38 GMT 2025
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CFR |
21 CFR 522.883
Created by
admin on Mon Mar 31 18:02:38 GMT 2025 , Edited by admin on Mon Mar 31 18:02:38 GMT 2025
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DEA NO. |
9059
Created by
admin on Mon Mar 31 18:02:38 GMT 2025 , Edited by admin on Mon Mar 31 18:02:38 GMT 2025
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Code System | Code | Type | Description | ||
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DTXSID00160254
Created by
admin on Mon Mar 31 18:02:38 GMT 2025 , Edited by admin on Mon Mar 31 18:02:38 GMT 2025
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PRIMARY | |||
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Etorphine hydrochloride
Created by
admin on Mon Mar 31 18:02:38 GMT 2025 , Edited by admin on Mon Mar 31 18:02:38 GMT 2025
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PRIMARY | |||
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13764-49-3
Created by
admin on Mon Mar 31 18:02:38 GMT 2025 , Edited by admin on Mon Mar 31 18:02:38 GMT 2025
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PRIMARY | |||
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DBSALT000825
Created by
admin on Mon Mar 31 18:02:38 GMT 2025 , Edited by admin on Mon Mar 31 18:02:38 GMT 2025
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PRIMARY | |||
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8CBE01N748
Created by
admin on Mon Mar 31 18:02:38 GMT 2025 , Edited by admin on Mon Mar 31 18:02:38 GMT 2025
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PRIMARY | |||
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23623749
Created by
admin on Mon Mar 31 18:02:38 GMT 2025 , Edited by admin on Mon Mar 31 18:02:38 GMT 2025
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PRIMARY | |||
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237-364-7
Created by
admin on Mon Mar 31 18:02:38 GMT 2025 , Edited by admin on Mon Mar 31 18:02:38 GMT 2025
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PRIMARY | |||
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300000023792
Created by
admin on Mon Mar 31 18:02:38 GMT 2025 , Edited by admin on Mon Mar 31 18:02:38 GMT 2025
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PRIMARY | |||
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C83705
Created by
admin on Mon Mar 31 18:02:38 GMT 2025 , Edited by admin on Mon Mar 31 18:02:38 GMT 2025
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PRIMARY |
Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |