Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C20H22N2O2.ClH |
| Molecular Weight | 358.862 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.COC1=CC2=C(C=CN=C2C=C1)C(=O)[C@@H]3C[C@@H]4CC[N@]3C[C@@H]4C=C
InChI
InChIKey=WWVHPDZMERMOBW-XITGISAOSA-N
InChI=1S/C20H22N2O2.ClH/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;1H/t13-,14-,19-;/m0./s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Ground and excited electronic states of quininone-containing Re(I)-based rectangles: a comprehensive study of their preparation, electrochemistry, and photophysics. | 2009-04-20 |
|
| Electrodes modified with monoolein cubic phases hosting laccases for the catalytic reduction of dioxygen. | 2004-01-15 |
|
| Metabolism and elimination of quinine in healthy volunteers. | 2003-09 |
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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. | 2003-02-14 |
|
| Simultaneous determination of quinine and four metabolites in plasma and urine by high-performance liquid chromatography. | 2001-04-15 |
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059Y922D24
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72710653
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6119-73-9
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m9449
Created by
admin on Mon Mar 31 23:02:50 GMT 2025 , Edited by admin on Mon Mar 31 23:02:50 GMT 2025
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PRIMARY | Merck Index |
SUBSTANCE RECORD
