Q3625

Chinidin

sodium channel blocker

• Empirische Formel (Hill-System): C₂₀H₂₄N₂O₂
• CAS-Nummer: 56-54-2
• Molekulargewicht: 324.42
• Beilstein: 91866
• EG-Nummer: 200-279-0
• MDL-Nummer: MFCD00135581
• UNSPSC-Code: 12352200
• PubChem Substanz-ID: 24899331
• NACRES: NA.77

Eigenschaften

• product name: Chinidin, anhydrous
• Qualität: anhydrous
• Qualitätsniveau: 200
• Verunreinigungen: ≤20% Dihydroquinidine (according to USP specifications., actual content given on label)
• mp (Schmelzpunkt): 168-172 °C (lit.)
• Ersteller: 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
• InChIKey: LOUPRKONTZGTKE-LHHVKLHASA-N
• Angaben zum Gen: 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)

Beschreibung

Anwendung

Quinidine has been used:

• 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. Wirkung

Quinidine, an isomer of quinine has potential side effects like proarrhythmia on usage. It prolongs cardiac potential and is sodium channel blocker. It is a potential antagonist for α1-adrenoceptors and contributes to hypotension. It inhibits cytochrome P450 2D6 and improves circulation and brain penetration of dementia drug, dextromethorphan. Quinidine-dextromethorphan combination may be useful in treating pseudobulbar affect (PBA).

Klasse IA antiarrhythmisch; blockiert Kaliumkanäle

Leistungsmerkmale und Vorteile

This compound is a featured product for ADME Tox research. Click here to discover more featured ADME Tox products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

This compound was developed by Bayer. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Sicherheitshinweise

• Piktogramme: GHS06
• Signalwort: Danger
• H-Sätze: H301,H317
• P-Sätze: P261 - P264 - P272 - P280 - P301 + P310 - P302 + P352
• Gefahreneinstufungen: Acute Tox. 3 Oral - Skin Sens. 1
• Lagerklassenschlüssel: 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
• WGK: WGK 1
• Persönliche Schutzausrüstung: dust mask type N95 (US), Eyeshields, Faceshields, Gloves