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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
Structure of ETORPHINE HYDROCHLORIDE

SMILES

Cl.[H][C@@]12OC3=C(O)C=CC4=C3[C@@]15CCN(C)[C@]([H])(C4)[C@@]56C[C@]([H])([C@](C)(O)CCC)[C@]2(OC)C=C6

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

HIDE SMILES / InChI

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.

Approval Year

PubMed

PubMed

TitleDatePubMed
Actions of etorphine hydrochloride, (M99): a potent morphine-like agent.
1967 May
Effect of benzodiazepines on the central action of narcotic analgesics.
1982
Negative feedback regulation of the content of proenkephalin mRNA in chromaffin cell cultures.
1988 Apr

Sample Use Guides

African Buffalo (700 kg bw) - 7.5-15 ug/kg African elephant (5000 kg bw) - 1-1,25 ug/kg Black Rhino (1000 kg bw) - 2-4 ug/kg
Route of Administration: Intramuscular
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:36:11 GMT 2023
Edited
by admin
on Fri Dec 15 15:36:11 GMT 2023
Record UNII
8CBE01N748
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETORPHINE HYDROCHLORIDE
GREEN BOOK   MART.  
Common Name English
ETORPHINE HCL
Common Name English
ETORPHINE HYDROCHLORIDE [MART.]
Common Name English
(6R,7R,14R)-7,8-DIHYDRO-7-((1R)-1-HYDROXY-1-METHYLBUTYL)-6-O-METHYL-6,14.ALPHA.-ETHENOMORPHINE HYDROCHLORIDE
Common Name English
19-PROPYLORVINOL HYDROCHLORIDE
Common Name English
M-99
Code English
M. 99
Code English
ETORPHINE HYDROCHLORIDE [GREEN BOOK]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C67413
Created by admin on Fri Dec 15 15:36:11 GMT 2023 , Edited by admin on Fri Dec 15 15:36:11 GMT 2023
CFR 21 CFR 522.883
Created by admin on Fri Dec 15 15:36:11 GMT 2023 , Edited by admin on Fri Dec 15 15:36:11 GMT 2023
DEA NO. 9059
Created by admin on Fri Dec 15 15:36:11 GMT 2023 , Edited by admin on Fri Dec 15 15:36:11 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID00160254
Created by admin on Fri Dec 15 15:36:11 GMT 2023 , Edited by admin on Fri Dec 15 15:36:11 GMT 2023
PRIMARY
WIKIPEDIA
Etorphine hydrochloride
Created by admin on Fri Dec 15 15:36:11 GMT 2023 , Edited by admin on Fri Dec 15 15:36:11 GMT 2023
PRIMARY
CAS
13764-49-3
Created by admin on Fri Dec 15 15:36:11 GMT 2023 , Edited by admin on Fri Dec 15 15:36:11 GMT 2023
PRIMARY
DRUG BANK
DBSALT000825
Created by admin on Fri Dec 15 15:36:11 GMT 2023 , Edited by admin on Fri Dec 15 15:36:11 GMT 2023
PRIMARY
FDA UNII
8CBE01N748
Created by admin on Fri Dec 15 15:36:11 GMT 2023 , Edited by admin on Fri Dec 15 15:36:11 GMT 2023
PRIMARY
PUBCHEM
23623749
Created by admin on Fri Dec 15 15:36:11 GMT 2023 , Edited by admin on Fri Dec 15 15:36:11 GMT 2023
PRIMARY
ECHA (EC/EINECS)
237-364-7
Created by admin on Fri Dec 15 15:36:11 GMT 2023 , Edited by admin on Fri Dec 15 15:36:11 GMT 2023
PRIMARY
SMS_ID
300000023792
Created by admin on Fri Dec 15 15:36:11 GMT 2023 , Edited by admin on Fri Dec 15 15:36:11 GMT 2023
PRIMARY
NCI_THESAURUS
C83705
Created by admin on Fri Dec 15 15:36:11 GMT 2023 , Edited by admin on Fri Dec 15 15:36:11 GMT 2023
PRIMARY
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ACTIVE MOIETY