CAS 131929-60-7
:Espinosina A
Descrição:
Espinosina A é um inseticida de origem natural derivado da fermentação da bactéria do solo Saccharopolyspora spinosa. Pertence à classe de compostos conhecidos como espinosad, que são caracterizados por sua estrutura única com um sistema de anel tetracíclico. Espinosina A exibe um amplo espectro de atividade inseticida, particularmente contra pragas lepidópteras, tornando-o valioso em aplicações agrícolas. Funciona ao interromper o funcionamento normal do sistema nervoso do inseto, levando à paralisia e à morte. O composto é conhecido por sua baixa toxicidade para mamíferos e insetos benéficos, o que o torna uma alternativa ecológica aos pesticidas sintéticos. Espinosina A também é estável sob várias condições ambientais, contribuindo para sua eficácia no manejo de pragas. Seu uso é regulamentado em muitos países e frequentemente é encontrado em formulações para agricultura orgânica. No geral, Espinosina A é reconhecido por sua eficácia, perfil de segurança e impacto mínimo em organismos não-alvo, alinhando-se com práticas agrícolas sustentáveis.
Fórmula:C41H65NO10
InChI:InChI=1S/C41H65NO10/c1-10-26-12-11-13-34(52-36-17-16-33(42(5)6)23(3)48-36)22(2)37(44)32-20-30-28(31(32)21-35(43)50-26)15-14-25-18-27(19-29(25)30)51-41-40(47-9)39(46-8)38(45-7)24(4)49-41/h14-15,20,22-31,33-34,36,38-41H,10-13,16-19,21H2,1-9H3/t22-,23-,24+,25-,26+,27-,28-,29-,30-,31+,33+,34+,36+,38+,39-,40-,41+/m1/s1
Chave InChI:InChIKey=SRJQTHAZUNRMPR-UYQKXTDMSA-N
SMILES:O([C@H]1C[C@]2([C@]3([C@]([C@]4(C(=C3)C(=O)[C@H](C)[C@@H](O[C@@H]5O[C@H](C)[C@@H](N(C)C)CC5)CCC[C@H](CC)OC(=O)C4)[H])(C=C[C@@]2(C1)[H])[H])[H])[H])[C@H]6[C@H](OC)[C@H](OC)[C@@H](OC)[C@H](C)O6
Sinónimos:- (-)-Spinosyn A
- (2R,3aS,5aR,5bS,9S,13S,14R,16aS,16bR)-13-{[(2R,5S,6R)-5-(dimethylamino)-6-methyltetrahydro-2H-pyran-2-yl]oxy}-9-ethyl-14-methyl-7,15-dioxo-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-1H-as-indaceno[3,2-d]oxacyclododecin-2-yl 6-deoxy-2,3,4-tri-O-methyl-alpha-L-mannopyranoside
- (2R,3aS,5aR,5bS,9S,13S,14R,16aS,16bR)-2-[(6-Deoxy-2,3,4-tri-O-methyl-α-<span class="text-smallcaps">L</span>-mannopyranosyl)oxy]-13-[[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,5a,5b,6,9,10,11,12,13,14,16a,16b-tetradecahydro-14-methyl-1H-as-indaceno[3,2-d]oxacyclododecin-7,15-dione
- (2R,3aS,5aR,5bS,9S,14R,16aS,16bR)-13-{[(2R,5S,6R)-5-(dimethylamino)-6-methyltetrahydro-2H-pyran-2-yl]oxy}-9-ethyl-14-methyl-7,15-dioxo-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-1H-as-indaceno[3,2-d]oxacyclododecin-2-yl 6-deoxy-2,3,4-tri-O-methyl-alpha-L-mannopyranoside
- (5aR,5bS,14R,16bR)-13-{[5-(dimethylamino)-6-methyltetrahydro-2H-pyran-2-yl]oxy}-9-ethyl-14-methyl-7,15-dioxo-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-1H-as-indaceno[3,2-d]oxacyclododecin-2-yl 6-deoxy-2,3,4-tri-O-methylhexopyranoside
- 1H-as-Indaceno[3,2-d]oxacyclododecin-7,15-dione, 2-[(6-deoxy-2,3,4-tri-O-methyl-α-<span class="text-smallcaps">L</span>-mannopyranosyl)oxy]-13-[[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,5a,5b,6,9,10,11,12,13,14,16a,16b-tetradecahydro-14-methyl-, (2R,3aS,5aR,5bS,9S,13S,14R,16aS,16bR)-
- 2-D)Oxacyclododecin-7,15-Dione,2,3,3A,5A,5B,6,9,10,11,12,13,14,16A,16B-Tetradecahydro-2-((6-Deoxy-2,3,4-Tri-O-Methyl-Alpha-L-Mannopyranosyl)Oxy)-13-((5-Dimethylamino)Tetrahydro-6-Methyl-2H-Pyran-2-Yl)
- A 83543A
- Lepicidin A
- Mixture of Spinosyn A and Spinosyn D
- Spinosad A
- spinosyn D
- (2R,3aS,5aR,5bS,9S,13S,14R,16aS,16bR)-2-[(6-Deoxy-2,3,4-tri-O-methyl-α-L-mannopyranosyl)oxy]-13-[[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,5a,5b,6,9,10,11,12,13,14,16a,16b-tetradecahydro-14-methyl-1H-as-indaceno[3,2-d]oxacyclododecin-7,15-dione
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Pureza (%)
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100
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0
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50
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90
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95
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100
11 produtos.
(2R,3aS,5aR,5bS,9S,13S,14R,16aS,16bR)-2-[(6-Deoxy-2,3,4-tri-O-methyl-α-L-mannopyranosyl)oxy]-13-[[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,5a,5b,6,9,10,11,12,13,14,16a,16b-tetradecahydro-14-methyl-1H-as-indaceno[3,2-d]oxacyclododecin-7,15-dione
CAS:Fórmula:C41H65NO10Pureza:90%Cor e Forma:SolidPeso molecular:731.9555Spinosyn A
CAS:<p>Spinosyn A is a polyketide-derived macrolide produced by Saccharopolyspora spinosa and is an active ingredient in several commercial insecticides.</p>Fórmula:C41H65NO10Pureza:90.06%Cor e Forma:SolidPeso molecular:731.96GB 23200.121-2021 Pesticide Mixture 7 50 µg/mL in Acetonitrile
CAS:Produto Controlado- 1014-70-6
- 102851-06-9
- 10369-83-2
- 105843-36-5
- 120067-83-6
- 121552-61-2
- 122-34-9
- 130000-40-7
- 131549-75-2
- 131929-60-7
- 131929-63-0
- 135410-20-7
- 138261-41-3
- 148-79-8
- 150824-47-8
- 165252-70-0
- 1912-24-9
- 21087-64-9
- 210880-92-5
- 21725-46-2
- 33629-47-9
- 40487-42-1
- 41483-43-6
- 53112-28-0
- 5915-41-3
- 7287-19-6
- 75736-33-3
- 834-12-8
- 862588-11-2
- 865318-97-4
- 96525-23-4
Cor e Forma:MixtureSpinosyn A 100 µg/mL in Acetonitrile
CAS:Produto ControladoFórmula:C41H65NO10Cor e Forma:Single SolutionPeso molecular:731.96Spinosad
CAS:Fórmula:C41H65NO10(A)C42H67NO10(D)Pureza:≤ 5.0%Cor e Forma:White or almost white crystalline powderPeso molecular:731.95 (A); 745.98 (D)Spinosyn A
CAS:<p>Applications Spinosyn A is a potent insecticide for pathogens of crops and disruptor of nicotinic acetylcholine receptor.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>Fórmula:C41H65NO10Cor e Forma:Off-WhitePeso molecular:731.96Spinosyn A
CAS:<p>Spinosyn A is a natural insecticide, which is derived from the fermentation of the soil bacterium *Saccharopolyspora spinosa*. It exhibits a unique mode of action as it targets the nicotinic acetylcholine receptors of the insect nervous system. This interaction results in hyperexcitation of the insect neurons, leading to paralysis and ultimately death.</p>Fórmula:C41H65NO10Pureza:Min. 95%Peso molecular:731.96 g/mol









