Structure via PubChem · Public domain (PubChem)
Key facts
- Drug.IUPAC_name
- Mixture of:(10E,14E,16E)-(1R,4S,5′S,6S,6′R,8R,12S,13S,20R,21R,24S)-6′-[(S)-sec-butyl]-21,24-dihydroxy-5′,11,13,22-tetramethyl-2-oxo-(3,7,19-trioxatetracyclo[15.6.1.14,8.020,24]pentacosa-10,14,16,22-tetraene)-6-spiro-2′-(5′,6′-dihydro-2′H-pyran)-12-yl 2,6-dideoxy-4-O-(2,6-dideoxy-3-O-methyl-α-L-arabino-hexopyranosyl)-3-O-methyl-α-L-arabino-hexopyranosideand(10E,14E,16E)-(1R,4S,5′S,6S,6′R,8R,12S,13S,20R,21R,24S)-21,22-dihydroxy-6′-isopropyl-5′,11,13,22-tetramethyl-2-oxo-(3,7,19-trioxatetracyclo[15.6.1.14,8.020,24]pentacosa-10,14,16,22-tetraene)-6-spiro-2′-(5′,6′-dihydro-2′H-pyran)-12-yl 2,6-dideoxy-4-O-(2,6-dideoxy-3-O-methyl-α-L-arabino-hexopyranosyl)-3-O-methyl-α-L-arabino-hexopyranoside
- Drug.image
- Avermectins.png
- Drug.image_class
- skin-invert-image
- Drug.width
- 300
- Drug.imageL
- Abamectin B1a.png
- Drug.image_classL
- bg-transparent
- Drug.widthL
- 150
- Drug.imageR
- Abamectin B1b.png
- Drug.image_classR
- bg-transparent
- Drug.widthR
- 150
- Drug.legal_AU
- S5
- Drug.legal_AU_comment
- /S6
- Drug.Jmol
- None
- Drug.CAS_number
- 71751-41-2
- Drug.ATCvet
- yes
- Drug.ATC_prefix
- P54
- Drug.ATC_suffix
- AA02
- Drug.ChemSpiderID
- 8095964
via Wikipedia infobox
Chemical data
- Formula
- C95H142O28
- Molecular weight
- 1732.1 g/mol
- IUPAC name
- (1'R,2R,3S,4'S,6S,8'R,10'E,12'S,13'S,14'E,16'E,20'R,21'R,24'S)-2-butan-2-yl-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-3,11',13',22'-tetramethylspiro[2,3-dihydropyran-6,6'-3,7,19-trioxatetracyclo[15.6.1.14,8.020,24]pentacosa-10,14,16,22-tetraene]-2'-one;(1'R,2R,3S,4'S,6S,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-3,11',13',22'-tetramethyl-2-propan-2-ylspiro[2,3-dihydropyran-6,6'-3,7,19-trioxatetracyclo[15.6.1.14,8.020,24]pentacosa-10,14,16,22-tetraene]-2'-one
- SMILES
- CCC(C)[C@@H]1[C@H](C=C[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.C[C@H]1/C=C/C=C/2\CO[C@H]3[C@@]2([C@@H](C=C([C@H]3O)C)C(=O)O[C@H]4C[C@@H](C/C=C(/[C@H]1O[C@H]5C[C@@H]([C@H]([C@@H](O5)C)O[C@H]6C[C@@H]([C@H]([C@@H](O6)C)O)OC)OC)\C)O[C@]7(C4)C=C[C@@H]([C@H](O7)C(C)C)C)O
- InChIKey
- IBSREHMXUMOFBB-MVGRHBATSA-N
- Polar surface area
- 340 Ų
- H-bond donors
- 6
- H-bond acceptors
- 28
- Formal charge
- 0
via PubChem
Research
1,304 papers- Abamectin as a pesticide for agricultural use.Acta Leidensia · 1990
- Abamectin promotes behavior changes and liver injury in zebrafish.Chemosphere · 2023
- Abamectin Causes Neurotoxicity in Zebrafish Embryos.International journal of molecular sciences · 2025
- MRI brain findings of Abamectin toxic encephalopathy: a case report with review of literature.Emergency radiology · 2023
- Abamectin exposure causes chronic toxicity and trypsin/chymotrypsin damages in Chironomus kiiensis Tokunaga (Diptera: Chironomidae).Pesticide biochemistry and physiology · 2024
via PubMed