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product name
Quinidine, anhydrous
grade
anhydrous
impurities
≤20% Dihydroquinidine (according to USP specifications., actual content given on label)
mp
168-172 °C (lit.)
originator
Bayer
SMILES string
COc1ccc2nccc([C@H](O)C3CC4CCN3C[C@@H]4C=C)c2c1
InChI
1S/C20H24N2O2/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/h3-6,8,11,13-14,19-20,23H,1,7,9-10,12H2,2H3/t13-,14-,19+,20-/m0/s1
InChI key
LOUPRKONTZGTKE-LHHVKLHASA-N
Gene Information
human ... ABCB1(5243) , CYP2D6(1565) , CYP3A4(1576) , KCNH1(3756) , SCN10A(6336) , SCN11A(11280) , SCN1A(6323) , SCN2A(6326) , SCN3A(6328) , SCN4A(6329) , SCN5A(6331) , SCN7A(6332) , SCN8A(6334) , SCN9A(6335)
mouse ... Abcb1a(18671) , Abcb1b(18669)
rat ... Cyp2d1(266684) , Cyp2d2(25053) , Cyp2d3(24303) , Cyp2d4v1(171522)
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Application
- as an inhibitor of cytochrome P450 enzyme isoform CYP2D6
- as a potassium (K+) channel blocker in microglia
- to test its effect on electrophysiological behaviour of human induced pluripotent stem cells (hiPSC) cardiomyocytes
Biochem/physiol Actions
Features and Benefits
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Skin Sens. 1
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 1
Personal Protective Equipment
Certificates of Analysis (COA)
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