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Emetine (hydrochloride hydrate)

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    Emetine (hydrochloride hydrate)
  • Emetine (hydrochloride hydrate)
Cat No: 21048
Cayman

Emetine is an alkaloid that has been found in ipecac root and has diverse biological activities.{53660,31081,36705,53655} It is active against several strains of E. histolytica amoebae (IC50s = 0.73-10.22 μg/ml).{53660} Emetine inhibits NF-κB signalin...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • (2S,3R,11bS)-3-ethyl-1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-2-[[(1R)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-isoquinolinyl]methyl]-2H-benzo[a]quinolizine, dihydrochloride, hydrate
Correlated keywords:
  • 483-18-1 316-42-7 NSC 33669 NSC33669 Cephaeline Emetin Entamoeba NF?B TNF? IL1? ME-180 HT-3 5HT 5HT3 anti-viral SARS-CoV-2 SARSCoV2 covid-19 covid19 coronavirus corona virus
Product Overview:
Emetine is an alkaloid that has been found in ipecac root and has diverse biological activities.{53660,31081,36705,53655} It is active against several strains of E. histolytica amoebae (IC50s = 0.73-10.22 μg/ml).{53660} Emetine inhibits NF-κB signaling induced by TNF-α or IL-1β (IC50s = 2 and 4.2 μM, respectively, in a cell-based β-lactamase reporter assay), increases caspase-3/7 activity in ME180 cells (EC50 = 1.1 μM), and is cytotoxic to HeLa cells.{31081} It reduces the infectious virus yield and viral RNA copy numbers in the culture supernatant of Vero E6 cells infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2; EC50s = 0.46 and 0.5 μM, respectively).{53655} Emetine (5 mg/kg) induces emesis in ferrets, an effect that can be prevented by the serotonin (5-HT) receptor subtype 5-HT3 antagonist ondansetron.{36705}
Size 25 mg
Shipping dry ice
CAS Number 7083-71-8
Molecular Formula C29H40N2O4 • 2HCl [XH2O]
SMILES CC[C@@H]1[C@@H](C[C@@]2(C3=CC(OC)=C(C=C3CCN2)OC)[H])C[C@]4(C5=CC(OC)=C(C=C5CCN4C1)OC)[H].Cl.Cl.O
Molecular Weight 553,6
Formulation A crystalline solid
Purity ≥85%
Custom Code 2939.79
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.

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