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
[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
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 |
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Target ID: CHEMBL237 Sources: http://www.ncbi.nlm.nih.gov/pubmed/2992058 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
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
by
admin
on
Edited
Fri Dec 15 15:36:11 GMT 2023
by
admin
on
Fri Dec 15 15:36:11 GMT 2023
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Record UNII |
2208ZLI77S
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C241
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2208ZLI77S
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72522-13-5
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DTXSID501024513
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3042090
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C033776
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Eptazocine
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1039
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m4966
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SUB06594MIG
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C72115
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100000084558
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5043
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CHEMBL70566
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Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
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ACTIVE MOIETY |