Quinine

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Quinine

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Cat No: 23958

Quinine is an alkaloid antimalarial agent that has MIC values ranging from 10 to 500 nM for 60 Thai isolates of P. falciparum.{39572} It inhibits hemozoin formation in purified trophozoites, leading to an increase in free heme, similar to the mechanis...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

(8?,9R)-6'-methoxy-cinchonan-9-ol

Correlated keywords:

6912-57-8 12239-42-8 21480-31-9 55980-20-6 72646-90-3 95650-40-1 128544-03-6 767303-40-2 840482-04-4 857212-53-4 864908-93-0 875538-34-4 888714-03-2 890027-24-4 894767-09-0 898813-59-7 898814-28-3 899813-83-3 900786-66-5 900789-95-9 906550-97-8 909263-47-4 909767-48-2 909882-78-6 910878-25-0 910880-97-6 911445-75-5 918778-04-8 1071756-51-8 1267651-57-9 1628705-47-4 anti-malarial Plasmodium Cinkona Mosgard QSM Qualaquin Quine 9 Quinex Quinlex Quinlup Rezquin SW-85833 SW85833 WR297608 WR-297608 NSC192949 6119-70-6 130-89-2

Product Overview:
Quinine is an alkaloid antimalarial agent that has MIC values ranging from 10 to 500 nM for 60 Thai isolates of P. falciparum.{39572} It inhibits hemozoin formation in purified trophozoites, leading to an increase in free heme, similar to the mechanism of action of chloroquine (Item No. 14194).{38381} In mice, quinine reduces P. berghei parasite load in the blood with a minimum effective dose (MED) of 150 mg/kg.{39573} Formulations containing quinine have been used in the treatment of uncomplicated malaria.

Size	1 g
Shipping	dry ice
CAS Number	130-95-0
Molecular Formula	C₂₀H₂₄N₂O₂
SMILES	COC1=CC=C2C(C([C@@H](O)[C@]3([H])C[C@H]4[C@@H](C=C)C[N@@]3CC4)=CC=N2)=C1
Molecular Weight	324,4
Formulation	A crystalline solid
Purity	≥95%
Custom Code	2933.39
UNSPSC code	12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

Accreditations
ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.