Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C20H22N2O2 |
Molecular Weight | 322.4009 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 4 / 4 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C2N=CC=C(C(=O)[C@@H]3C[C@@H]4CC[N@]3C[C@@H]4C=C)C2=C1
InChI
InChIKey=SRFCUPVBYYAMIL-NJSLBKSFSA-N
InChI=1S/C20H22N2O2/c1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18/h3-6,8,11,13-14,19H,1,7,9-10,12H2,2H3/t13-,14-,19-/m0/s1
Molecular Formula | C20H22N2O2 |
Molecular Weight | 322.4009 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Simultaneous determination of quinine and four metabolites in plasma and urine by high-performance liquid chromatography. | 2001 Apr 15 |
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Nuclear overexpression of NADH:cytochrome b5 reductase activity increases the cytotoxicity of mitomycin C (MC) and the total number of MC-DNA adducts in Chinese hamster ovary cells. | 2003 Feb 14 |
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Metabolism and elimination of quinine in healthy volunteers. | 2003 Sep |
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Electrodes modified with monoolein cubic phases hosting laccases for the catalytic reduction of dioxygen. | 2004 Jan 15 |
|
Ground and excited electronic states of quininone-containing Re(I)-based rectangles: a comprehensive study of their preparation, electrochemistry, and photophysics. | 2009 Apr 20 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:06:55 GMT 2023
by
admin
on
Sat Dec 16 10:06:55 GMT 2023
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Record UNII |
956671AJG7
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Record Status |
Validated (UNII)
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Record Version |
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