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340,000+ 研究の概要 · Triple ISO certified · COA & SDS すべての製品に適用 · 在庫品は当日出荷

Quinidine - Moligand™, ≥98%, contains 5-15% Dihydroquinidine , Channel blocker of K 2P10.1;Channel blocker of K 2P16.1;Channel blocker of K 2P18.1;Channel blocker of K 2P5.1;Channel blocker of K 2P6.1;Channel blocker of K Ca5.1;Channel blocker of K Na1.1;, Channel blocker of K 2P10.1;Channel blocker of K 2P16.1;Channel blocker of K 2P18.1;Channel blocker of K 2P5.1;Channel blocker of K 2P6.1;Channel blocker of K Ca5.1;Channel blocker of K Na1.1;Channel blocker of K Na1.2;Channel blocker of K v10.1;Channel b

CAS: 56-54-2 Cat. No.: Q109702 分子式: C20H24N2O2 分子量: 324.42 Beilstein Registry Number: 91866 EC番号: 200-279-0
21 Citations COA
Quinidine - Moligand™, ≥98%, contains 5-15% Dihydroquinidine CAS No(56-54-2) by Aladdin Scientific
注文可能
グレード＆純度 Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98% contains 5-15% Dihydroquinidine
Synonyms
(S)-(6-methoxy-4-quinolyl)-[(2R,4S,5R)-5-vinylquinuclidin-2-yl]methanol | (S)-Ethyl 2-amino-4-(methylthio)butanoate hydrochloride | (S)-(6-methoxyquinolin-4-yl)((2R,5R)-5-vinylquinuclidin-2-yl)methanol | Chinidine | CINCHONAN-9-0L, 6'-METHOXY-, (95)- | NC
Storage
Store at 2-8°C,Protected from light,Argon charged
Shipped In
Wet ice
★
サイズ
USA
ドイツ (EU)*
価格
個数
1g
Q109702-1g
1 在庫あり
—
$21.90
5g
Q109702-5g
3 在庫あり
—
$29.90
25g
Q109702-25g
3 在庫あり
—
$89.90
100g
Q109702-100g
3 在庫あり
—
$246.90
Enter a quantity for the sizes you want to add.
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データシート
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仕様書
仕様 名前と識別子 ドキュメント 詳細データ Taxonomic Classification 3 D構造 関連ターゲット（人間） 関連ターゲット（非人間） 作用メカニズム 証明書（CoA、COO、BSE/TSEと分析図） 化学的性質と物理的性質 よくある質問と記事 Citations of This Product ソリューション計算機 レビュー よくある質問
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このグレードを選ぶ理由

Moligand™, ≥98%, contains 5-15% Dihydroquinidine Moligand™ ベースライン干渉を最小限に抑える必要がある、感度の高いクロマトグラフィーおよび分析ワークフロー向け。

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保管・配送

Store at 2-8°C,Protected from light,Argon charged Wet ice に出荷。正確な仕様については、ロット固有の COA をご確認ください。

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品質書類

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文献的裏付け

クロマトグラフィー、有機合成、クロスカップリング反応に関する 21 件の査読済み論文で引用されています。

仕様

同義語
(S)-(6-methoxy-4-quinolyl)-[(2R,4S,5R)-5-vinylquinuclidin-2-yl]methanol | (S)-Ethyl 2-amino-4-(methylthio)butanoate hydrochloride | (S)-(6-methoxyquinolin-4-yl)((2R,5R)-5-vinylquinuclidin-2-yl)methanol | Chinidine | CINCHONAN-9-0L, 6'-METHOXY-, (95)- | NC
仕様と純度
Moligand™, ≥98%, contains 5-15% Dihydroquinidine
生化学的・生理学的メカニズム
Class IA antiarrythmic; reduces both Na+and K+channel currents, including INa, IKrand IKs. Prolongs QT and induces torsade de pointes (TdP).
保管条件
Store at 2-8°C,Protected from light,Argon charged
入荷
Wet ice
この製品は冷冷この冷このこの製品の運送が必要です。地上およびその他の経済サービスは利用できません。
等級
Moligand™
アクションタイプ
CHANNEL BLOCKER, INHIBITOR
作用メカニズム
Channel blocker of K 2P10.1;Channel blocker of K 2P16.1;Channel blocker of K 2P18.1;Channel blocker of K 2P5.1;Channel blocker of K 2P6.1;Channel blocker of K Ca5.1;Channel blocker of K Na1.1;Channel blocker of K Na1.2;Channel blocker of K v10.1;Channel b
純度
≥98%
名前と識別子
パブケム・シド
504758745
パブケム・シド・ウル
https://pubchem.ncbi.nlm.nih.gov/substance/504758745
カノニカル・スマイル
COC1=CC2=C(C=CN=C2C=C1)C(C3CC4CCN3CC4C=C)O
IUPAC Name
(S)-[(2R,4S,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanol
InChIKey
LOUPRKONTZGTKE-LHHVKLHASA-N
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
異性体SMILES
COC1=CC2=C(C=CN=C2C=C1)[C@@H]([C@H]3C[C@@H]4CCN3C[C@@H]4C=C)O
WGKドイツ
3
RTECS
VA4725000
UN番号
2811
包装グループ
I
分子量
324.42
Beilstein
91866
Reaxy-Rn
91864
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=91864&ln=

ドキュメント

📋 安全データシート（SDS）

危険性、取扱い、保管、および規制遵守を網羅した包括的な文書。

<<<<<<< HEAD SDS をダウンロード → ======= SDS をダウンロード → >>>>>>> release248-p3

✅ 分析証明書（COA）

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📊 データシート

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詳細データ

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassAlkaloids and derivatives
分類Cinchona alkaloids
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentCinchona alkaloids
Alternative Parents 4-quinolinemethanols  Quinuclidines  Anisoles  Aralkylamines  Alkyl aryl ethers  Pyridines and derivatives  Piperidines  Heteroaromatic compounds  Trialkylamines  Secondary alcohols  1,2-aminoalcohols  Azacyclic compounds  Organopnictogen compounds  Hydrocarbon derivatives  Aromatic alcohols  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Cinchonan-skeleton - 4-quinolinemethanol - Quinoline - Anisole - Quinuclidine - Alkyl aryl ether - Aralkylamine - Piperidine - Pyridine - Benzenoid - Heteroaromatic compound - 1,2-aminoalcohol - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Ether - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Amine - Alcohol - Organic oxygen compound - Aromatic alcohol - Aromatic heteropolycyclic compound
説明This compound belongs to the class of organic compounds known as cinchona alkaloids. These are alkaloids structurally characterized by the presence of the cinchonan skeleton, which consists of a quinoline linked to an azabicyclo[2.2.2]octane moiety.
External Descriptors cinchona alkaloid
3 D構造
インタラクティブ化学構造モデル





関連ターゲット（人間）
CYP2D6 Tclin Cytochrome P450 2D6 (50 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ABCB1 Tchem Multidrug resistance protein 1 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNA7 Tclin Potassium voltage-gated channel subfamily A member 7 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SLC29A4 Tchem Equilibrative nucleoside transporter 4 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SCN5A Tclin Sodium channel protein type 5 subunit alpha (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNK5 Tchem Potassium channel subfamily K member 5 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNH1 Tclin Potassium voltage-gated channel subfamily H member 1 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNK6 Tbio Potassium channel subfamily K member 6 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNK18 Tclin Potassium channel subfamily K member 18 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNH5 Tclin Potassium voltage-gated channel subfamily H member 5 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNH2 Tclin Potassium voltage-gated channel subfamily H member 2 (6 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNK10 Tclin Potassium channel subfamily K member 10 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNK16 Tbio Potassium channel subfamily K member 16 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNA4 Tclin Potassium voltage-gated channel subfamily A member 4 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNT1 Tchem Potassium channel subfamily T member 1 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNT2 Tchem Potassium channel subfamily T member 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNU1 Tbio Potassium channel subfamily U member 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNA5 Tclin Potassium voltage-gated channel subfamily A member 5 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCND2 Tclin Potassium voltage-gated channel subfamily D member 2 (1 Activities)
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ESR1 Tclin Estrogen receptor alpha (17718 Activities)
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PGR Tclin Progesterone receptor (8562 Activities)
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ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
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CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
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ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)
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HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
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ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
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ACHE Tclin Acetylcholinesterase (18204 Activities)
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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
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SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
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HRH2 Tclin Histamine H2 receptor (5428 Activities)
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HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
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HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
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AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)
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ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
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AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)
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SLC6A4 Tclin Serotonin transporter (12625 Activities)
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PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
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HRH1 Tclin Histamine H1 receptor (7573 Activities)
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OPRM1 Tclin Mu opioid receptor (19785 Activities)
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OPRD1 Tclin Delta opioid receptor (15096 Activities)
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HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)
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ADORA2A Tclin Adenosine A2a receptor (16305 Activities)
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BDKRB2 Tclin Bradykinin B2 receptor (3970 Activities)
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Abcb1b P-glycoprotein 1 (174 Activities)
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Cavia porcellus (23802 Activities)
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Mus musculus (284745 Activities)
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Rattus norvegicus (775804 Activities)
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LLC-PK1 (2135 Activities)
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MDCK (10148 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ScN2a (522 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Kcnk9 Potassium channel subfamily K member 9 (8 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ferriprotoporphyrin IX (165 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
norA Quinolone resistance protein norA (2171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Cholinesterase (8742 Activities)
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Leishmania mexicana mexicana (27 Activities)
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Brain (1 Activities)
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Plasma (328 Activities)
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Heart (171 Activities)
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Aorta (2975 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cerebrospinal fluid (288 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Kcnb1 Potassium voltage-gated channel subfamily B member 1 (9 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc22a5 Solute carrier family 22 member 5 (44 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mdr1a Multidrug resistance protein 1a (106 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slco1a1 Solute carrier organic anion transporter family member 1A1 (265 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slco1a4 Solute carrier organic anion transporter family member 1A4 (114 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc22a4 Solute carrier family 22 member 4 (11 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Scn2a Sodium channel alpha subunits; brain (Types I, II, III) (344 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
作用メカニズム
証明書（CoA、COO、BSE/TSEと分析図）
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

9 results found

Lot NumberCertificate Type日付商品
G2227342G2227342Certificate of AnalysisMay 19, 2026 Q109702
G2227343G2227343Certificate of AnalysisMay 19, 2026 Q109702
G2227344G2227344Certificate of AnalysisMay 19, 2026 Q109702
G2227345G2227345Certificate of AnalysisMay 19, 2026 Q109702
D2621118D2621118Certificate of AnalysisApr 30, 2026 Q109702
G2115271G2115271Certificate of AnalysisApr 03, 2025 Q109702
I2004158I2004158Certificate of AnalysisJul 12, 2024 Q109702
I2016279I2016279Certificate of AnalysisJul 12, 2024 Q109702
B2512086B2512086Certificate of AnalysisJun 14, 2022 Q109702
化学的性質と物理的性質
溶解度Solvent:DMSO, Max Conc. mg/mL: 32.44, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 8.11, Max Conc. mM: 25
感度Light sensitive；heat sensitive
融点（°C）170-175°C
分子量324.400 g/mol
XLogP32.900
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count4
Exact Mass324.184 Da
Monoisotopic Mass324.184 Da
Topological Polar Surface Area45.600 Ų
Heavy Atom Count24
Formal Charge0
Complexity457.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
よくある質問と記事
ADME/Tox: From Basics to Advanced – Metabolizing Enzymes, Transporters and Key Tool Compounds
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
ADME/Tox
Chiral Amines in Asymmetric Synthesis: Role Map (A–F), a Minimal Evidence Chain, and a Research Selection Guide (with Tables 1–3)
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Asymmetric synthesis Chiral amine
Cinchona Alkaloid Chiral Toolbox: Selection & Troubleshooting from Pseudoenantiomer Switching to PTC/Sharpless AD/Chiral Resolution (including Product Tables A–D)
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
alkaloids chirality basic nitrogen-containing compounds
Quinoline vs Isoquinoline: How “Where the Nitrogen Sits” Changes Reactivity and Applications
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Drug discovery Materials chemistry Quinoline Isoquinoline N-heteroaromatics
Experimental Selection Logic for Phase-Transfer Catalysts: Choosing Catalysts by Phase-State System, Source of Anionic Species, and Reaction Task
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Phase-Transfer Catalysis PTC
Why Small Molecules Can Also Serve as Catalysts: Judging Organocatalytic Systems from Reaction Objectives and Activatable Structural Sites
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Organocatalyst
Citations of This Product
How to Cite Aladdin Scientific Products? Citations Search
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よくある質問

What is the purity of this product?
This product is supplied at ≥98% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.
What is Moligand??
Moligand? is one of Aladdin Scientific's premium product lines, formulated for high-purity applications across multiple workflows. Compared to standard grades in the same workflow, Moligand? products typically offer tighter specifications, more rigorous QC, and stronger lot-to-lot consistency.
How should this product be stored?
Store at 2–8 °C, protected from light, under argon. It is supplied under an argon blanket; reseal under inert gas after each use.
How is this product shipped?
This product ships chilled on wet ice. Unpack on arrival and transfer it to the storage condition stated above.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 56-54-2, the molecular formula is C20H24N2O2, and the molecular weight is 324.42 g/mol. InChIKey LOUPRKONTZGTKE-LHHVKLHASA-N.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

📚 用途別の引用文献

Electrochemistry & battery electrolyte2
Spectroscopy sample preparation3
Extraction & workup solvent3
Organic synthesis — reaction medium5
Polymer synthesis & polymerization1
Chromatography (HPLC / GC / TLC)2
Drug / compound screening11
Cytotoxicity screening9
Cell viability3
Other applications3
Nanoparticle / material biocompatibility1
21 件の引用文献をすべて見る →

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