Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C21H28N2OS |
Molecular Weight | 356.525 |
Optical Activity | ( + ) |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]1(CCCC[C@H]1N2CCCC2)N(C)C(=O)CC3=C4C=CSC4=CC=C3
InChI
InChIKey=SYHJZCCNQDFHJQ-RTBURBONSA-N
InChI=1S/C21H28N2OS/c1-22(18-8-2-3-9-19(18)23-12-4-5-13-23)21(24)15-16-7-6-10-20-17(16)11-14-25-20/h6-7,10-11,14,18-19H,2-5,8-9,12-13,15H2,1H3/t18-,19-/m1/s1
Molecular Formula | C21H28N2OS |
Molecular Weight | 356.525 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Highly selective kappa opioid analgesics. 4. Synthesis of some conformationally restricted naphthalene derivatives with high receptor affinity and selectivity. | 1991 Jan |
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Kappa opioid receptor agonists inhibit the pilocarpine-induced seizures and toxicity in the mouse. | 1994 Dec |
|
Differential effects of fedotozine compared to other kappa agonists on diuresis in rats. | 1996 Dec |
|
Potentiation of kappa-opioid receptor agonist-induced analgesia and hypothermia by fluoxetine. | 2001 May-Jun |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:05:06 GMT 2023
by
admin
on
Sat Dec 16 08:05:06 GMT 2023
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Record UNII |
T1I84BQJ6E
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Record Status |
Validated (UNII)
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Record Version |
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T1I84BQJ6E
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122115
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114419-77-1
Created by
admin on Sat Dec 16 08:05:07 GMT 2023 , Edited by admin on Sat Dec 16 08:05:07 GMT 2023
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Related Record | Type | Details | ||
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ENANTIOMER -> ENANTIOMER |
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RACEMATE -> ENANTIOMER |
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