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
SMILES
CN1CC[C@]2(C)C[C@@H](CC3=C2C=C(O)C=C3)C1
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
| 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 |
DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/15278579
Sources: http://www.ncbi.nlm.nih.gov/pubmed/15278579
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
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL233 Sources: http://www.ncbi.nlm.nih.gov/pubmed/2992058 |
|||
Target ID: CHEMBL237 Sources: http://www.ncbi.nlm.nih.gov/pubmed/2992058 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
29.97 ng/mL |
15 mg single, subcutaneous dose: 15 mg route of administration: Subcutaneous experiment type: SINGLE co-administered: |
EPTAZOCINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
34.86 ng/mL |
15 mg single, intramuscular dose: 15 mg route of administration: Intramuscular experiment type: SINGLE co-administered: |
EPTAZOCINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
82.34 ng × h/mL |
15 mg single, subcutaneous dose: 15 mg route of administration: Subcutaneous experiment type: SINGLE co-administered: |
EPTAZOCINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
95.64 ng × h/mL |
15 mg single, intramuscular dose: 15 mg route of administration: Intramuscular experiment type: SINGLE co-administered: |
EPTAZOCINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
119.1 μg × min/mL |
60 mg single, intravenous dose: 60 mg route of administration: Intravenous experiment type: SINGLE co-administered: NITROUS OXIDE |
EPTAZOCINE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
143.6 μg × min/mL |
90 mg single, intravenous dose: 90 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
EPTAZOCINE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
1.77 h |
15 mg single, subcutaneous dose: 15 mg route of administration: Subcutaneous experiment type: SINGLE co-administered: |
EPTAZOCINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1.66 h |
15 mg single, intramuscular dose: 15 mg route of administration: Intramuscular experiment type: SINGLE co-administered: |
EPTAZOCINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
108.9 min |
60 mg single, intravenous dose: 60 mg route of administration: Intravenous experiment type: SINGLE co-administered: NITROUS OXIDE |
EPTAZOCINE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
110.3 min |
90 mg single, intravenous dose: 90 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
EPTAZOCINE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN |
Sample Use Guides
In Vivo Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/2724517
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
Sources: http://www.ncbi.nlm.nih.gov/pubmed/2992058
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
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Edited
Mon Mar 31 18:02:37 GMT 2025
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2208ZLI77S
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NCI_THESAURUS |
C241
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C033776
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Eptazocine
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m4966
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C72115
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CHEMBL70566
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