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Details

Stereochemistry ABSOLUTE
Molecular Formula C15H21NO
Molecular Weight 231.3333
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EPTAZOCINE

SMILES

[H][C@@]12CC3=C(C=C(O)C=C3)[C@@](C)(C1)CCN(C)C2

InChI

InChIKey=ZOWQTJXNFTWSCS-IAQYHMDHSA-N
InChI=1S/C15H21NO/c1-15-5-6-16(2)10-11(9-15)7-12-3-4-13(17)8-14(12)15/h3-4,8,11,17H,5-7,9-10H2,1-2H3/t11-,15-/m1/s1

HIDE SMILES / InChI

Molecular Formula C15H21NO
Molecular Weight 231.3333
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Eptazocine is an opioid analgesic which was introduced in 1987 by Morishita in Japan . It acts as a mixed κappa opioid receptor agonist and mu-opioid receptor antagonist.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown

Sample Use Guides

In Vivo Use Guide
The induction of anesthesia was started with eptazocine 30 mg iv and thiopental 3-4 mg.kg-1 iv and the trachea was intubated smoothly following succinylcholine 40 mg iv. Then, they were given intravenous droperidol 0.15 mg.kg-1 with inhalation of 70% N2O and 30% O2. Good intraoperative muscle relaxation was obtained by dialferine or pancuronium.
Route of Administration: Intravenous
In Vitro Use Guide
Eptazocine caused a concentration-dependent inhibition against the [3H]-naloxone [( 3H]-NLX) specific binding to rat brain synaptic membrane in the absence of sodium cation and GTP (IC50; 7.83 +/- 1.57 microM). The ratios of IC50 values between the absence to the presence of sodium cation alone or sodium cation and GTP were 3.89 and 4.35, respectively. In addition, eptazocine (10 microM) also produced the significant decrease of [3H]-NLX specific binding in the mouse brain synaptic membrane
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
2208ZLI77S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EPTAZOCINE
INN   MI   WHO-DD  
INN  
Official Name English
eptazocine [INN]
Common Name English
Eptazocine [WHO-DD]
Common Name English
(-)-(1S,6S)-2,3,4,5,6,7-HEXAHYDRO-1,4-DIMETHYL-1,6-METHANO-1H-4-BENZAZONIN-10-OL
Systematic Name English
EPTAZOCINE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C241
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
FDA UNII
2208ZLI77S
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
72522-13-5
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
EPA CompTox
DTXSID501024513
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
3042090
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
MESH
C033776
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
Eptazocine
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 CENTRAL
1039
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
MERCK INDEX
m4966
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 Merck Index
EVMPD
SUB06594MIG
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
C72115
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
100000084558
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
INN
5043
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
ChEMBL
CHEMBL70566
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
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY