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Ivermectin B1a

Base Information
  • Chemical Name:Ivermectin B1a
  • CAS No.:70161-11-4
  • Deprecated CAS:123022-60-6,139645-33-3,70161-11-4,73910-57-3,116522-39-5,116522-39-5,139645-33-3,70161-11-4,73910-57-3,923580-16-9
  • Molecular Formula:C48H74O14
  • Molecular Weight:875.099
  • Hs Code.:
  • European Community (EC) Number:276-046-2,274-536-0,615-075-0
  • UNII:91Y2202OUW
  • DSSTox Substance ID:DTXSID8023181
  • Wikipedia:Ivermectin
  • Wikidata:Q27132923
  • NCI Thesaurus Code:C61796
  • RXCUI:6069
  • Metabolomics Workbench ID:63058
  • ChEMBL ID:CHEMBL263291
  • Mol file:70161-11-4.mol
Ivermectin B1a

Synonyms:Eqvalan;Ivermectin;Ivomec;Mectizan;MK 933;MK-933;MK933;Stromectol

Suppliers and Price of Ivermectin B1a
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 16 raw suppliers
Chemical Property of Ivermectin B1a
Chemical Property:
  • Boiling Point:940.4oC at 760mmHg 
  • Flash Point:267.3oC 
  • PSA:170.06000 
  • Density:1.23g/cm3 
  • LogP:5.60140 
  • XLogP3:4.1
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:14
  • Rotatable Bond Count:8
  • Exact Mass:874.50785703
  • Heavy Atom Count:62
  • Complexity:1680
Purity/Quality:

98% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Drug Classes:Anthelmintic Agents
  • Canonical SMILES:CCC(C)C1C(CCC2(O1)CC3CC(O2)CC=C(C(C(C=CC=C4COC5C4(C(C=C(C5O)C)C(=O)O3)O)C)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)O)OC)OC)C)C
  • Isomeric SMILES:CC[C@H](C)[C@@H]1[C@H](CC[C@@]2(O1)C[C@@H]3C[C@H](O2)C/C=C(/[C@H]([C@H](/C=C/C=C/4\CO[C@H]5[C@@]4([C@@H](C=C([C@H]5O)C)C(=O)O3)O)C)O[C@H]6C[C@@H]([C@H]([C@@H](O6)C)O[C@H]7C[C@@H]([C@H]([C@@H](O7)C)O)OC)OC)\C)C
  • Recent ClinicalTrials:Safety of a Single Dose of Moxidectin Compared With Ivermectin in Individuals Living in Onchocerciasis Endemic Areas and in Individuals Living in Onchocerciasis Endemic Areas With High Levels of Lymphatic Filariasis Co-endemicity Receiving Concomitant Albendazole
  • Recent EU Clinical Trials:A multicentre randomised, Double-Blind, Placebo-controlled, Study to evaluate the efficAcy and safety of oral IVErmectin tablets in the prevention of COVID-19 (the SAIVE Trial)
  • Recent NIPH Clinical Trials:double-blind study in COvid-19 patients with iveRmectin
  • Uses Ivermectin B1a (dihydroavermectin B1a) is the major component (>80%) of the commercial anthelmintic, ivermectin. Members of the avermectin/milbemycin anthelmintic class exert their anthelmintic effects by binding to glutamate-gated chloride channels expressed on nematode neurones and pharyngeal muscle cells. The avermectins and milbemycins are also potent insecticides. The individual 25-sec-butyl (B1a) and 25-iso-propyl (B1b) components of ivermectin have received little separate study.
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