Ivermectin

Ivermectin Struktur
70288-86-7
CAS-Nr.
70288-86-7
Bezeichnung:
Ivermectin
Englisch Name:
Ivermectin
Synonyma:
IVERMECTINE;IVOMEC;IVERMECTIN HCL;VERMECTIN;Stromectol;Ivermectin EP2000;Avermectin B1a Dihydro Analog;mk933;Uvemec;Vermic
CBNumber:
CB0415655
Summenformel:
C48H74O14
Molgewicht:
875.09
MOL-Datei:
70288-86-7.mol

Ivermectin Eigenschaften

alpha 
D +71.5 ± 3° (c = 0.755 in chloroform)
RTECS-Nr.
IH7891500
storage temp. 
2-8°C
Löslichkeit
H2O: ≤1.0% KF
Aggregatzustand
powder
Farbe
White
Wasserlöslichkeit
4mg/L(temperature not stated)
BCS Class
4/3
Stabilität:
Stable for 2 years as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 3 months.
InChIKey
AZSNMRSAGSSBNP-XPNPUAGNSA-N
CAS Datenbank
70288-86-7(CAS DataBase Reference)
EPA chemische Informationen
Ivermectin (70288-86-7)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher T,Xn,T+
R-Sätze: 61-25-36-36/38-22-28
S-Sätze: 53-26-45-36-36/37-28
RIDADR  UN 2811 6.1/PG 2
WGK Germany  3
HazardClass  6.1(a)
PackingGroup  II
HS Code  29322090
Toxizität LD50 in dogs, rhesus monkeys (mg/kg): about 80, more than 24 orally. (MSDS Merck & Co. Inc., 2003)
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H300 Lebensgefahr bei Verschlucken. Akute Toxizität oral Kategorie 2 Achtung GHS hazard pictogramssrc="/GHS06.jpg" width="20" height="20" /> P264, P270, P301+P310, P321, P330,P405, P501
H311 Giftig bei Hautkontakt. Akute Toxizität dermal Kategorie 3 Achtung GHS hazard pictogramssrc="/GHS06.jpg" width="20" height="20" /> P280, P302+P352, P312, P322, P361,P363, P405, P501
H410 Sehr giftig für Wasserorganismen mit langfristiger Wirkung. Langfristig (chronisch) gewässergefährdend Kategorie 1 Warnung GHS hazard pictogramssrc="/GHS09.jpg" width="20" height="20" /> P273, P391, P501
Sicherheit
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P273 Freisetzung in die Umwelt vermeiden.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P301+P310 BEI VERSCHLUCKEN: Sofort GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.

Ivermectin Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R61:Kann das Kind im Mutterleib schädigen.
R25:Giftig beim Verschlucken.
R36:Reizt die Augen.
R36/38:Reizt die Augen und die Haut.
R22:Gesundheitsschädlich beim Verschlucken.

S-Sätze Betriebsanweisung:

S53:Exposition vermeiden - vor Gebrauch besondere Anweisungen einholen.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.

Beschreibung

Ivermectin is an antiparasitic agent effective in the treatment of onchocerciasis, or "river blindness". Since ivermectin acts to prevent the adult worm from producing microfilariae, it needs to be administered only once or twice a year.

Chemische Eigenschaften

Crystalline Solid

Verwenden

Semi-synthetic derivative of Abamectin; consists of a mixture of not less than 80% component B1a and not more than 20% component B1b. Antihelmintic (Onchocerca)

synthetische

The synthesis of ivermectin involves the hydrogenation of the naturally occurring avermectin B1 (abamectin) at the double bond linking C-22 and C-23. This results in a mixture of two homologues, 22, 23-dihydroavermectin B1a (H2B1a) and 22, 23-dihydroavermectin B1b (H2 B1b). The a- and b- nomenclature refers to the presence on C-25, of either a secondary butyl side chain or an isopropyl group, respectively. The biological activities of H2B1a and H2B1b are similar. Large-scale separation of the two homologues is not practical, and, hence, ivermectin is marketed as a mixture of H2 B1a (>80%) and H2 B1b (<20%).

Indications

Ivermectin (Mectizan) acts on parasite-specific inhibitory glutamate-gated chloride channels that are phylogenetically related to vertebrate GABA-gated chloride channels. Ivermectin causes hyperpolarization of the parasite cell membrane and muscle paralysis.At higher doses it can potentiate GABA-gated chloride channels. It does not cross the blood-brain barrier and therefore has no paralytic action in mammals, since GABA-regulated transmission occurs only in the central nervous system (CNS). Ivermectin is administered by the oral and subcutaneous routes. It is rapidly absorbed. Most of the drug is excreted unaltered in the feces. The half-life is approximately 12 hours.

Antimicrobial activity

It is also active against O. volvulus and other filarial worms, but the effect is chiefly directed against the larval forms (microfilariae). Uniquely among anthelmintic agents it exhibits activity against some ectoparasites, including Sarcoptes scabiei.

Biologische Aktivität

Positive allosteric modulator of the α 7 neuronal nicotinic acetylcholine receptor and the purinergic P2X 4 receptor. Antihelmintic. Also modulates glutamate- and GABA-activated chloride channels. Potentiates glycine-gated currents at low concentrations (30 nM).

Clinical Use

Onchocerciasis
Non-disseminated strongyloidiasis
Lymphatic filariasis (in combination with albendazole)
Scabies
If the patient is harboring Asc. lumbricoides, the worms will be passed in the feces. Head lice will also be killed, which is very much welcomed by the treated patients. Ivermectin has been widely used in the veterinary field, where use is also made of its effect on ectoparasites.

Nebenwirkungen

In the treatment of onchocerciasis mild Mazzotti-type reactions occur, with occasional neurological problems. Although it is highly effective against L. loa, care must be taken to avoid treating patients with high microfilarial counts: there is one report of a patient with a concomitant L. loa infection who died when treated for onchocerciasis. Mild gastrointestinal and nervous system signs may occur following treatment for strongyloidiasis.

Stoffwechsel

Ivermectin is rapidly absorbed, is bound to a great extent to plasma protein, and is excreted in the urine or feces either unchanged or as the 3′-O-demethyl-22,23-dihydroavermectin B1α or as the dihydroavermectin B1α monosaccharide. The absorption of IVM is significantly affected by the presence of alcohol. Administration of IVM as an alcoholic solution may result in as much as a 100% increase in absorption.

Ivermectin Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Ivermectin Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 797)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hebei ZB Gamay Biological Technology Co.,Ltd
+86-031189171450 +86-15632359451
chem@zbvet.net China 222 58
Masteam Bio-tech Co., Ltd.
+86-15200345168 +86-15200345168
bruce.lei@masteam.com CHINA 153 58
Hebei Guanlang Biotechnology Co., Ltd.
+86-19930503282
alice@crovellbio.com China 8823 58
Hebei Miaoyin Technology Co.,Ltd
+86-17367732028 +86-17367732028
kathy@hbyinsheng.com China 3582 58
Hebei Lingding Biotechnology Co., Ltd.
+86-18031140164 +86-19933155420
erin@hbldbiotech.com China 878 58
Sinoway Industrial co., ltd.
0592-5800732; +8613806035118
xie@china-sinoway.com China 992 58
Hebei Mojin Biotechnology Co., Ltd
+8613288715578
sales@hbmojin.com China 12456 58
Shanghai Affida new material science and technology center
+undefined15081010295
2691956269@qq.com China 359 58
Shaanxi TNJONE Pharmaceutical Co., Ltd
+8618740459177
sarah@tnjone.com China 893 58
XI'AN TIANGUANGYUAN BIOTECH CO., LTD.
+86-029-86333380 18829239519
sales06@tgybio.com China 959 58

70288-86-7(Ivermectin)Verwandte Suche:


  • IVERMECTIN NOT LESS THAN 93.0% OF 22,23-DIHY- DROAVERMECTIN B1A, AND NOT LESS THAN 97.0% OF 22,23-DIHY-DROAVERMECTIN B1(B1A+B1B)
  • IVERMECTIN EP(CRM STANDARD)
  • IVERMECTIN USP(CRM STANDARD)
  • IvermectineEp2000
  • IVERMECTIN
  • heartgard-30
  • EQVALEN
  • CARDOMEC
  • mk933
  • 22,23-DIHYDROAVERMECTIN B1
  • 22,23-DIHYDROAVERMECTINE
  • 22,23-Dihydroavemectin B1
  • Ivermectin (200 mg)
  • Ivermectin (200 mg)G0D4080.906mg/mg(ai)
  • IverMectin(FDA)
  • Ivermectin,22,23-Dihydroavermectin B1, MK-933
  • IverMectin, USP
  • (1'R,2R,4'S,5S,6R,8'R,10'E,12'S,13'S,14'E,16'E,20'R,21'R,24'S)-21',24'-dihydroxy-12'-{[(2R,4S,5S,6S)-5-{[(2S,4S,5S,6S)-5-hydroxy-4-Methoxy-6-Methyloxan-2-yl]oxy}-4-Methoxy-6-Methyloxan-2-yl]oxy}-5,11',13',22'-tetraMethyl-6-(propan-2-yl)-3',7',19'-trioxasp
  • IverMectin COS
  • IvetMectin
  • Ivermectine 0
  • IVERMECTINE(PATENT-NOSUPPLY)
  • 22,23-Dihydro C-076B1
  • Ivosint
  • Mectizan
  • Uvemec
  • Vermic
  • Zimecterin
  • 22,23-Dihydroavermectin B1, MK-933
  • Ivermectin (EDMF)
  • Ivermecti
  • 22,23-Dihydro C-076 Bla
  • 22,23-Dihydro C-176B
  • 22,23-Dihydroabamectin
  • 22,23-Dihydroavermectin Bla
  • 22,23-Dihydroavermectin Blb
  • 5-O-Demethyl-22,23-dihydmavermectin Ala
  • Cardotek-30:Eqvalan
  • hyvermectin
  • mk-0933
  • Ivermectin, >=98%
  • 23-Dihydroavermectin B1
  • Ivermectin 70288-86-7
  • High purity Ivermectin 99% in stock CAS NO.70288-86-7 CAS NO.70288-86-7
  • Ivermectin, 98.5%
  • Cardomec(TM)
  • Lvermectin1
  • Ivermectine, ≥98%
  • Ivermectin@1000 μg/mL in Acetonitrile
  • Ivermectin CRS
  • Ivermectin@100 μg/mL in Acetonitrile
  • 70288-86-7 Ivermectin Bio Pesticides for nematodes / insects / miticides
  • Veterinary Drug Ivermectin
  • Ivermectin USP/EP/BP
  • Ivermectinr
  • IvermectinCAS
  • IvermectinQ: What is Ivermectin Q: What is the CAS Number of Ivermectin Q: What is the storage condition of Ivermectin Q: What are the applications of Ivermectin
  • Ivermectin D2Q: What is Ivermectin D2 Q: What is the CAS Number of Ivermectin D2 Q: What is the storage condition of Ivermectin D2 Q: What are the applications of Ivermectin D2
Copyright 2019 © ChemicalBook. All rights reserved