Weight | 326.44 g/mol |
---|---|
Formula | C20H26N2O2 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 4 |
522-66-7 (522-66-7)
hydroquinine · dihydroquinidine · hydroquinidine
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- Theoretical Study on the Origin of Enantioselectivity in the Bis(dihydroquinidine)-3,6-pyridazineOsmium Tetroxide-Catalyzed Dihydroxylation of Styrene (Journal of the American Chemical Society, 1999)
- The first reagent-controlled asymmetric halolactonizations. Dihydroquinidine-halogen complexes as chiral sources of positive halogen ion (Canadian Journal of Chemistry, 1998)
- Potent inhibition of yeast-expressed CYP2D6 by dihydroquinidine, quinidine, and its metabolites (Biochemical Pharmacology, 1995)
- Plasma concentrations of quinidine, its major metabolites, and dihydroquinidine in patients with torsades de pointes. (Clinical Pharmacology & Therapeutics, 1988)
- Randomised controlled trial of hydroquinine in muscle cramps (The Lancet, 1997)
- Comparative in vitro electrophysiology of quinidine, its major metabolites and dihydroquinidine. (Journal of Pharmacology and Experimental Therapeutics, 1987)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - hydroquinine
- dihydroquinidine
- hydroquinidine
- dihydroquinine
- hydroquinidine monosulfate, (1beta,3alpha,4beta,9S)-isomer
- hydroquinidine hydrochloride
- hydroquinidine, (3alpha,9S)-(+-)-isomer
- hydroquinidine, (9S)-(+-)-isomer
- hydroquinidine monosulfate
- LCN 834
- Lentoquine
- hydroquinidine dihydrochloride, (1beta,4beta,3S)-(+-)-isomer
- hydroquinidine, (1beta, 3alpha,4beta,8alpha,9R)-isomer
- hydroquinidine dihydrochloride, (3alpha,9S)-(+-)-isomer
- hydroquinidine, (8alpha,9S)-isomer
- hydroquinidine sulfate, (9S)-isomer
- LCN-834
- Srcor
- hydroquinidine sulfate
- hydroquinidine monosulfate, (1beta,3alpha,4beta,8alpha,9R)-isomer
- hydroquinidine, (+-)-isomer
- hydroquinidine, (8alpha,9R)-isomer
- hydroquinidine, (9R)-isomer
- hydroquinidine, (1beta,3alpha,4beta,9S)-isomer
- hydroquinidine, (1beta,4beta,9S)-(+-)-isomer
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SMILESCCC1CN2CCC1CC2C(C3=C4C=C(C=CC4=NC=C3)OC)O
-
InChIKeyLJOQGZACKSYWCH-UHFFFAOYSA-N
- Pubchem - 522-66-7
- Wikipedia - hydroquinine
Dihydroquinine, also known as hydroquinine, is an organic compound and as a cinchona alkaloid closely related to quinine. The specific rotation is 148 in ethanol. A derivative of this molecule is used as chiral ligand in the AD-mix for Sharpless dihydroxylation.
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