Emetin, seine Salze undVerbindungen

Emetine Struktur
483-18-1
CAS-Nr.
483-18-1
Bezeichnung:
Emetin, seine Salze undVerbindungen
Englisch Name:
Emetine
Synonyma:
C09421;EMetin;EMETINE;Emetine (>Ipecac alkali;EMetine (>90%);EMETINE USP/EP/BP;Emetine HCL BP/USP;Cephaeline methyl ether;6',7',10,11-Tetramethoxymetan
CBNumber:
CB6512352
Summenformel:
C29H40N2O4
Molgewicht:
480.64
MOL-Datei:
483-18-1.mol

Emetin, seine Salze undVerbindungen Eigenschaften

Schmelzpunkt:
89-96°C
alpha 
D20 -50° (c = 2 in CHCl3)
Siedepunkt:
578.63°C (rough estimate)
Dichte
1.1174 (rough estimate)
Brechungsindex
1.5800 (estimate)
storage temp. 
-20°C Freezer
Löslichkeit
Soluble in Water (100 mg/ml)
Aggregatzustand
solid
pka
5.77, 6.64(at 25℃)
Farbe
White
Wasserlöslichkeit
961.3mg/L(15 ºC)
Stabilität:
Stable for 2 years from date of purchase as supplied. Solutions in water may be stored at -20°C for up to 3 months.

Sicherheit

RIDADR  1544
HazardClass  6.1(b)
PackingGroup  III
Giftige Stoffe Daten 483-18-1(Hazardous Substances Data)
Toxizität LD50 i.p. in rats: 12.1 mg/kg (Radomski)

Emetin, seine Salze undVerbindungen Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften

Brown Solid

Verwenden

Emetine is the principal alkaloid of ipecac, the ground roots of Uragoga ipecacuanha.

Definition

ChEBI: Emetine is a pyridoisoquinoline comprising emetam having methoxy substituents at the 6'-, 7'-, 10- and 11-positions. It is an antiprotozoal agent and emetic. It inhibits SARS-CoV2, Zika and Ebola virus replication and displays antimalarial, antineoplastic and antiamoebic properties. It has a role as an antiprotozoal drug, a plant metabolite, an antiviral agent, an emetic, a protein synthesis inhibitor, an antimalarial, an antineoplastic agent, an autophagy inhibitor, an antiinfective agent, an expectorant, an anticoronaviral agent and an antiamoebic agent. It is a pyridoisoquinoline and an isoquinoline alkaloid. It is functionally related to a cephaeline. It is a conjugate base of an emetine(2+). It derives from a hydride of an emetan.

Indications

Chlorprothixene (Taractan) has been reported twice to be effective in the treatment of PHN. For severe pain, an initial 50 to 100 mg IM injection has been advocated. Otherwise, the dosage is 25 to 50 mg PO q6h. The recommended duration of therapy is 4 to 10 days. Higher doses are unwarranted and frequently result in side effects.

Weltgesundheitsorganisation (WHO)

Emetine, an alkaloid obtained from ipecacuanha, was first used rationally as an amoebocide in 1912. It was subsequently widely used and was included in earlier editions of the WHO Model List of Essential Drugs but has now been replaced by the less cardiotoxic synthetic derivative dehydroemetine. Although it is valuable in the treatment of systemic amoebic hepatitis it has now been largely superseded by considerably less toxic drugs, and in particular by metronidazole.

Hazard

Toxic by ingestion.

Health Hazard

The toxicity of cephaeline is lower than thatof emetine. The toxic effects are cumulative. Ingestion of high doses may producehypotension, muscle weakness, and gastroin testinal problems, including nausea, vomit ing, and diarrhea.

Mechanism of action

This drug has a direct amebicidal effect against trophozoites E. histolytica in tissues, and it is not active against cysts in either the lumen or intestinal walls, or in other organs. The mechanism of action of emetine consists of the blockage of protein synthesis in eukaryotic (but not in prokaryotic) cells. It inhibits the process of polypeptide chain formation. Protein synthesis is inhibited in parasite and mammalian cells, but not in bacteria.
Emetine is currently only used as a drug for treating amebiasis in cases of resistance to other drugs. Synonyms of this drug are ipecin and methylcefalin.

Einzelnachweise

1) Lee et al. (2008), Ipecacuanha: the South American vomiting root; J R Coll. Physicians Edinb., 38 355
2) Sun et al. (2019), Emetine Exhibits Anticancer Activity in Breast Cancer Cells as an Antagonist of Wnt/β-catenin Signaling; Oncol. Rep., 42 1735 DOI:10.3892/or.2019.7290
3) Yang et al. (2018), Changing cancer survival in China during 2003-2015: a pooled analysis of 17 population-based cancer registries; Cell Discov., 4 31
4) Choy et al. (2020), Remdesivir, Lopinavir, and Homoharringtonine Inhibit SARS-CoV-2 Replication in Vitro; Antivir. Res., 178 104786 DOI:10.1016/j.antiviral.2020.104786
5) Cuyas et al. (2015), Anti-protozoal and Anti-Bacterial Antibiotics That Inhibit Protein Synthesis Kill Cancer Subtypes Enriched for Stem Cell-Like Properties; Cell Cycle, 14 3527
DOI:10.1080/15384101.2015.1044173
6) Application of emetine in SARS-CoV-2 treatment: regulation of p38 MAPK signaling pathway for preventing emetine-induced cardiac complications DOI:10.1080/15384101.2022.2100575
7) Emetine, a potent alkaloid for the treatment of SARS-CoV-2 targeting papain-like protease and non-structural proteins: pharmacokinetics, molecular docking and dynamic studies DOI:10.1080/07391102.2021.1946715
8) A Comprehensive Guide to the Hazardous Properties of Chemical Substances
9) Manual of Dermatologic Therapeutics with Essentials of Diagnosis, 7th Edition
10) Consolidated List of Products whose Consumption

Emetin, seine Salze undVerbindungen Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Emetin, seine Salze undVerbindungen Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 40)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Aktin Chemicals, Inc.
028-85159085
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1026@dideu.com China 29220 58
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+8618058761490
info@gihichemicals.com China 49999 58
J & K SCIENTIFIC LTD. 010-82848833 400-666-7788
jkinfo@jkchemical.com China 94838 76
Chemsky(shanghai)International Co.,Ltd. 021-50135380
shchemsky@sina.com China 32344 50
Beijing Jin Ming Biotechnology Co., Ltd. 010-60605840 18892239720
psaitong@jm-bio.com China 12308 58
Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 13028896684
sales@rrkchem.com China 55717 58
Chengdu Alfa Biotechnology Co.,Ltd. 028-028-85142057 19983342022
3005359975@qq.com China 1949 58

483-18-1(Emetin, seine Salze undVerbindungen)Verwandte Suche:


  • EMETINE
  • (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.
  • EMetin
  • Emetine HCL BP/USP
  • 6',7',10,11-Tetramethoxymetan
  • Cephaeline methyl ether
  • Canforemetina、Emetine Hydrochloride
  • Emetine (base and/or unspecified salts)
  • (1R)-1-[[(2S,3R,11bS)-3-Ethyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizine-2-yl]methyl]-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline
  • 6',7',10,11-Tetramethoxyemetan
  • C09421
  • EMetine (>90%)
  • 2H-Benzo[a]quinolizine, 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]-, (2S,3R,11bS)-
  • Emetine (>
  • EMETINE USP/EP/BP
  • Ipecac alkali
  • 483-18-1
  • Chiral Reagents
  • Impurities
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
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