Avermectin A1a, 5-O-demethyl-22,23-dihydro-

Avermectin A1a, 5-O-demethyl-22,23-dihydro- Suppliers list
Company Name: TargetMol Chemicals Inc.
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Products Intro: Product Name:Ivermectin B1a
CAS:71827-03-7
Package:1 mg;1 mL * 10mM (in DMSO);10 mg;100 mg;25 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Shanghai Acmec Biochemical Technology Co., Ltd.
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Products Intro: Product Name:Ivermectin B1a
CAS:71827-03-7
Purity:98% Package:5mg
Company Name: Aladdin Scientific
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Products Intro: Product Name:Ivermectin B1a
CAS:71827-03-7
Purity:98% Package:$214.9/1mg;$450.9/5mg;Bulk package Remarks:98%
Company Name: Suzhou ARTK Medchem Co., Ltd.
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Products Intro: Product Name:Ivermectin2-epimer(DihydroAvermectinB1a)
CAS:71827-03-7
Purity:0.98 Package:100KG;25KG;10KG;1KG
Company Name: Molsyns Research  
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Products Intro: Product Name:Ivermectin 2-epimer (Dihydro Avermectin B1a)
CAS:71827-03-7
Purity:98% Package:25mg; 50mg;100mg and 1 g
Avermectin A1a, 5-O-demethyl-22,23-dihydro- Basic information
Product Name:Avermectin A1a, 5-O-demethyl-22,23-dihydro-
Synonyms:22,23-Dihydro-5-O-demethylavermectin A1a;5-O-Demethyl-22,23-dihydroavermectin A1a;Dihydroavermectin B1a;Ivermectin B1a;IvermectinH2B1a;(2Ae,4E,5'S,6S,6'R,7S,8E,11R,13R,15S,17ar,20R,20ar,20bs)-20,20B-dihydroxy-5',6,8,19-tetramethyl-6'-[(1S)-1-methylpropyl]-17-oxo-3',4',5',6,6',10,11,14,15,17,17A,20,20A,20B-tetradecahydro-2H,7H-spiro[11,15-methanofuro[4,3,2-pq][2,6]benzodioxacyclooctadecine-13,2'-pyran]-7-yl 2,6-dideoxy-4-o-(2,6-dideoxy-3-o-methyl-alpha-L-arabino-hexopyranosyl)-3-o-methyl-alpha-L-arabino-hexopyranoside;Avermectin A1a, 5-O-demethyl-22,23-dihydro-;Ivermectin Impurity 3
CAS:71827-03-7
MF:C48H74O14
MW:875.09
EINECS:276-046-2
Product Categories:Organics
Mol File:71827-03-7.mol
Avermectin A1a, 5-O-demethyl-22,23-dihydro- Structure
Avermectin A1a, 5-O-demethyl-22,23-dihydro- Chemical Properties
Melting point 155-157°
Boiling point 717.97°C (rough estimate)
density 1.0683 (rough estimate)
refractive index 1.6130 (estimate)
storage temp. Store at -20°C
solubility Soluble in DMSO
form solid
pka12.42±0.70(Predicted)
color white
Safety Information
MSDS Information
Avermectin A1a, 5-O-demethyl-22,23-dihydro- Usage And Synthesis
DescriptionIvermectin B1a is the main component (>80%) of the anthelmintic ivermectin, which also contains ivermectin B1b (<20%; ). It produces antiparasitic activity by binding to glutamate-gated chloride channels expressed on nematode neurons and pharyngeal muscle cells, inducing irreversible channel opening and very long-lasting hyperpolarization/depolarization of the neuron/muscle cell, thereby blocking further function (EC50 = 104 nM). Formulations containing ivermectin inhibit replication of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in Vero/hSLAM cells.
UsesIvermectin B1a-D2 is a deuterium labelled analogue of Ivermectin B1a (I940815), which is a major component of Ivermectin (I940800), a 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). An invitro inhibitor of SARS-CoV-2/ Covid-19.
DefinitionChEBI: A macrocyclic lactone that is avermectin B1a in which the double bond present in the spirocyclic ring system has been reduced to a single bond. It is the major component of ivermectin.
references[1] j. wolsetnholme and a. t. rogers. glutamate-gated chloride channels and the mode of action of the avermectin/milbemycin anthelmintics. parasitology131 suppl, s85-s95 (2005).
[2] s. gaisser, l. kellenberger, a. l. kaja, et al. direct production of ivermectin-like drugs after domain exchange in the avermectin polyketide synthase of streptomyces avermitilis atcc31272. organic & biomolecular chemistry 1(16), 2840-2847 (2003).
[3] j. p. arena, k. k. liu, p. s. paress, et al. the mechanism of action of avermectins in caenorhabditis elegans: correlation between activation of glutamate-sensitive chloride current, membrane binding, and biological activity. journal of parasitology 81, 286-294 (1995).
Avermectin A1a, 5-O-demethyl-22,23-dihydro- Preparation Products And Raw materials
Preparation Products4a-Hydroxy Ivermectin
Tag:Avermectin A1a, 5-O-demethyl-22,23-dihydro-(71827-03-7) Related Product Information
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