CAS 65195-51-9
:Avermectin A1a
Description:
Avermectin A1a, with the CAS number 65195-51-9, is a macrocyclic lactone compound that belongs to the class of avermectins, which are derived from the fermentation of the soil bacterium Streptomyces avermitilis. This compound exhibits potent antiparasitic and insecticidal properties, making it widely used in veterinary medicine and agriculture. Avermectin A1a functions by interfering with the neurotransmission in parasites, leading to paralysis and death. It is characterized by its complex molecular structure, which includes multiple rings and functional groups that contribute to its biological activity. The compound is typically administered in formulations that enhance its stability and efficacy. Avermectin A1a is known for its low toxicity to mammals, which makes it a preferred choice for treating parasitic infections in livestock and pets. However, it is important to handle it with care, as it can be harmful to non-target organisms, particularly aquatic life. Overall, Avermectin A1a is a significant agent in pest control and veterinary therapeutics.
Formula:C49H74O14
InChI:InChI=1S/C49H74O14/c1-12-26(2)43-29(5)18-19-48(63-43)24-35-21-34(62-48)17-16-28(4)42(60-40-23-38(54-10)45(32(8)58-40)61-39-22-37(53-9)41(50)31(7)57-39)27(3)14-13-15-33-25-56-46-44(55-11)30(6)20-36(47(51)59-35)49(33,46)52/h13-16,18-20,26-27,29,31-32,34-46,50,52H,12,17,21-25H2,1-11H3/b14-13+,28-16+,33-15+/t26-,27-,29-,31-,32-,34+,35-,36-,37-,38-,39-,40-,41-,42-,43+,44+,45-,46+,48+,49+/m0/s1
InChI key:InChIKey=AFSHKCWTGFDXJR-SQOHEDJBSA-N
SMILES:O[C@@]1/2[C@]3([C@H](OC)C(C)=C[C@]1(C(=O)O[C@@]4(C[C@]5(O[C@@](C4)(C/C=C(\C)/[C@@H](O[C@H]6C[C@H](OC)[C@@H](O[C@H]7C[C@H](OC)[C@@H](O)[C@H](C)O7)[C@H](C)O6)[C@@H](C)\C=C\C=C2/CO3)[H])O[C@]([C@H](CC)C)([C@@H](C)C=C5)[H])[H])[H])[H]
Synonyms:- Spiro[11,15-methano-2H,13H,17H-furo[4,3,2-pq][2,6]benzodioxacyclooctadecin-13,2′-[2H]pyran]-17-one, 7-[[2,6-dideoxy-4-O-(2,6-dideoxy-3-O-methyl-α-L-arabino-hexopyranosyl)-3-O-methyl-α-L-arabino-hexopyranosyl]oxy]-5′,6,6′,7,10,11,14,15,17a,20,20a,20b-dodecahydro-20b-hydroxy-20-methoxy-5′,6,8,19-tetramethyl-6′-(1-methylpropyl)-, [6S-[2aE,4E,6R*,7R*,8E,11S*,13R*[5′R*,6′S*(R*)],15R*,17aS*,20S*,20aS*,20bR*]]-
- Antibiotic C 076A1a
- [6S-[2aE,4E,6R*,7R*,8E,11S*,13R*[5′R*,6′S*(R*)],15R*,17aS*,20S*,20aS*,20bR*]]-7-[[2,6-Dideoxy-4-O-(2,6-dideoxy-3-O-methyl-α-L-arabino-hexopyranosyl)-3-O-methyl-α-L-arabino-hexopyranosyl]oxy]-5′,6,6′,7,10,11,14,15,17a,20,20a,20b-dodecahydro-20b-hydroxy-20-methoxy-5′,6,8,19-tetramethyl-6′-(1-methylpropyl)spiro[11,15-methano-2H,13H,17H-furo[4,3,2-pq][2,6]benzodioxacyclooctadecin-13,2′-[2H]pyran]-17-one
- Spiro[11,15-methano-2H,13H,17H-furo[4,3,2-pq][2,6]benzodioxacyclooctadecin-13,2′-[2H]pyran], avermectin A1a deriv.
- Avermectin A1a
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Found 4 products.
Avermectin A1a (>90%)
CAS:Formula:C49H74O14Purity:>90%Color and Shape:White To Off-WhiteMolecular weight:887.1Avermectin a1a
CAS:<p>Avermectin A1a is a macrocyclic lactone used primarily as an anthelmintic and insecticide. It is derived from the fermentation of the soil bacterium *Streptomyces avermitilis*. The compound works through a neurotoxic mode of action, binding to glutamate-gated chloride channels in nerve and muscle cells of invertebrates, leading to paralysis and subsequent death of the parasites. This mechanism is highly specific, primarily affecting nematodes and arthropods.</p>Formula:C49H74O14Purity:90%Molecular weight:887.1 g/mol




