Details
Stereochemistry | ACHIRAL |
Molecular Formula | C11H15NO |
Molecular Weight | 177.2429 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCN(CC)C(=O)C1=CC=CC=C1
InChI
InChIKey=JLNGEXDJAQASHD-UHFFFAOYSA-N
InChI=1S/C11H15NO/c1-3-12(4-2)11(13)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3
Molecular Formula | C11H15NO |
Molecular Weight | 177.2429 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Increased tumor necrosis factor-alpha and nitric oxide production by rat macrophages following in vitro stimulation and intravenous administration of the delta-opioid agonist SNC 80. | 2001 May 4 |
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The role of nitric oxide in the proconvulsant effect of delta-opioid agonist SNC80 in mice. | 2002 Aug 30 |
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Increased survival of tumor-bearing mice by the delta opioid SNC 80. | 2005 Nov-Dec |
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Easily accessible benzamide-derived P,O ligands (Bphos) for palladium-catalyzed carbon-nitrogen bond-forming reactions. | 2007 Feb 5 |
|
Comparative effects of insect repellent N,N-diethylbenzamide, N,N-diethylphenylacetamide, and N,N-diethyl-3- methylbenzamide aerosols on the breathing pattern and respiratory variables in mice. | 2010 May |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:00:37 GMT 2023
by
admin
on
Fri Dec 15 19:00:37 GMT 2023
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Record UNII |
3Y74433ZXI
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Record Status |
Validated (UNII)
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Record Version |
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C016089
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16060
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3Y74433ZXI
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DTXSID0051784
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15542
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rebemide
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216-912-9
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1696-17-9
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