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Merck
CN

Q1250

奎宁 半硫酸盐 一水合物

synthetic, ≥90% (HPLC), Potassium channel blocker

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关于此项目

经验公式(希尔记法):
C20H24N2O2 · 0.5H2O4S · H2O
化学文摘社编号:
分子量:
391.47
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352210
MDL number:
Beilstein/REAXYS Number:
6113937
Assay:
≥90% (HPLC)
Quality level:
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产品名称

奎宁 半硫酸盐 一水合物, synthetic, ≥90% (HPLC)

biological source

synthetic

Quality Level

assay

≥90% (HPLC)

mp

~225 °C (dec.) (lit.)

solubility

H2O: slightly soluble 1.2 mg/mL, ethanol: 8 mg/mL

antibiotic activity spectrum

parasites

mode of action

enzyme | inhibits

originator

Bayer

SMILES string

O.O.OS(O)(=O)=O.COc1ccc2nccc([C@@H](O)C3CC4CCN3C[C@@H]4C=C)c2c1.COc5ccc6nccc([C@@H](O)C7CC8CCN7C[C@@H]8C=C)c6c5

InChI

1S/2C20H24N2O2.H2O4S.2H2O/c2*1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18;1-5(2,3)4;;/h2*3-6,8,11,13-14,19-20,23H,1,7,9-10,12H2,2H3;(H2,1,2,3,4);2*1H2/t2*13-,14-,19-,20+;;;/m00.../s1

InChI key

ZHNFLHYOFXQIOW-LPYZJUEESA-N

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Application

Quinine hemisulfate salt monohydrate has been used as a stimuli to evaluate its influence on sensory and cognitive factors.

Biochem/physiol Actions

Quinine has analgesic property.
钾通道阻滞剂。抗疟疾
钾通道阻滞剂。抗疟疾、抗胆碱能、抗高血压和降血糖剂;最初从南美树木的金鸡纳科中分离出来的生物碱。

Features and Benefits

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.

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signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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E M Clement et al.
Neuropharmacology, 37(7), 945-951 (1998-10-17)
Quinine and quinidine are reported to potentiate the behavioural effects of serotonergic agents and monoamine uptake inhibitors. We have therefore investigated the presynaptic actions of quinine and quinidine on monoamine uptake and release in rat brain tissue in vitro. Quinidine
A Hedman et al.
Journal of pharmaceutical sciences, 87(4), 457-461 (1998-04-21)
The pharmacokinetic interaction between quinidine and digoxin in patients is well-known, in general requiring a dose reduction of digoxin in patients concomitantly treated with quinidine. Quinine, the diastereomer of quinidine, has not been as extensively studied in this respect. In
Elizabeth A Sneddon et al.
Alcoholism, clinical and experimental research, 43(2), 243-249 (2018-11-16)
Alcohol use disorder is characterized by compulsive alcohol intake, or drinking despite negative consequences. Previous studies have shown that female rodents have a heightened vulnerability to drug use across different stages of the addictive cycle, but no previous studies have
Both perceptual and conceptual factors influence taste-odor and taste-taste interactions
Frank RA, et al.
Perception & Psychophysics, 54(3), 343-354 (1993)
F A Santos et al.
European journal of pharmacology, 364(2-3), 193-197 (1999-02-05)
The effect of quinine, a cinchona alkaloid, was studied on gastrointestinal transit in mice. Intraperitoneal (i.p.) administration of quinine inhibited the intestinal propulsion of a charcoal suspension at a dose of 100 mg/kg, comparing favorably with 5 mg/kg morphine. In

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全球贸易项目编号

货号GTIN
Q1250-50G04061836687786
Q1250-10G04061836687779
Q1250-5G04061836687793

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