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| Product | Description | |
|---|---|---|
| Spinosyn A | Spinosyn A is a potent insecticide for pathogens of crops and disruptor of nicotinic acetylcholine receptor. Group: Biochemicals. Grades: Highly Purified. CAS No. 131929-60-7. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C41H65NO10. US Biological Life Sciences. |  Worldwide |
| Spinosyn A | Spinosyn A is the main component of the unusual hydrophobic macrolide complex isolated from Echinosaccharomyces. It is an effective pesticide for crop pathogens and control of ectoparasites of animals. Synonyms: Spinosad factor A; Lepicidin A. Grades: >99% by HPLC. CAS No. 131929-60-7. Molecular formula: C41H65NO10. Mole weight: 731.95. |  |
| Spinosyn A | Spinosyn A. Uses: For analytical and research use. Group: Pesticides & metabolites; pesticides & metabolites. Alternative Names: (-)-Spinosyn A, A 83543A, Spinosyn A, Spinosad A, Lepicidin A, (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 No. 131929-60-7. Molecular Formula: C41H65NO10. Mole Weight: 731.96. Catalog: APS131929607. SMILES: CC[C@H]1CCC[C@H] (O[C@H]2CC[C@@H] ([C@@H] (C)O2)N (C)C)[C@@H] (C)C (=O)C3=C[C@H]4[C@@H]5C[C@@H] (C[C@H]5C=C[C@@H]4C3CC (=O)O1)O[C@@H]6O[C@@H] (C)[C@H] (OC)[C@@H] (OC)[C@H]6OC. Format: Neat. |  |
| Spinosyn A 17-pseudoaglycone | It is an acid degradation product produced by selective hydrolysis of the more labile forosamine saccharide in the 17-position of spinosyn A. It has weak activity as an insecticide. Synonyms: A 83543A pseudoglycone; 2',3',4'-O-methyl-rhamnosyl tetracyclic spinosyn pseudoaglycone; (2R, 3aS, 5aR, 5bS, 9S, 13S, 14R, 16aS, 16bR)-9-ethyl-13-hydroxy-14-methyl-2-{[(3R, 4R, 5S, 6S)-3, 4, 5-trimethoxy-6-methyloxan-2-yl]oxy}-1H, 2H, 3H, 3aH, 5aH, 5bH, 6H, 7H, 9H, 10H, 11H, 12H, 13H, 14H, 15H, 16aH, 16bH-as-indaceno[3, 2-d]oxacyclododecane-7, 15-dione. Grades: >95% by HPLC. CAS No. 131929-68-5. Molecular formula: C33H50O9. Mole weight: 590.74. | |
| Spinosyn A aglycone | It is an acid degradation product produced by hydrolysis of both saccharide groups on spinosyn. It has only weak activity as an insecticide as the saccharides are considered essential for potent activity. Synonyms: (-)-spinosyn A aglycon; A 83543A Aglycon; (2R, 3aS, 5aR, 5bS, 9S, 13S, 14R, 16aS, 16bR)-9-ethyl-2, 13-dihydroxy-14-methyl-2, 3, 3a, 5a, 5b, 6, 9, 10, 11, 12, 13, 14, 16a, 16b-tetradecahydro-1H-as-indaceno[3, 2-d][1]oxacyclododecine-7, 15-dione. Grades: >95% by HPLC. CAS No. 149560-97-4. Molecular formula: C24H34O5. Mole weight: 402.52. | |
| Spinosyn D | Spinosyn D is a spinosoid that is a minor component of spinosad isolated from sugarcane S. spinosa. It is a potent insecticide for crop pathogens and ectoparasite control on animals. Synonyms: Lepicidin D; A 83543D; Spinosad factor D; 1H-as-Indaceno(3,2-d)oxacyclododecin-7,15-dione, 2-((6-deoxy-2,3,4-tri-O-methyl-a-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-4, 14-dimethyl-, (2S, 3aR, 5aS, 5bS, 9S, 13S, 14R, 16aS, 16bS)-. Grades: >99% by HPLC. CAS No. 131929-63-0. Molecular formula: C42H67NO10. Mole weight: 745.98. | |
| Spinosyn D | Spinosyn D is one of the major components of Spinosad (HY-138800). Spinosad is a natural pesticide that shows biological activity against a range of insects including Lepidoptera [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 131929-63-0. Pack Sizes: 1 mg. Product ID: HY-125326. |  |
| Spinosyn D 17-pseudoaglycone | It is an acid degradation product produced by selective hydrolysis of the more labile forosamine saccharide in the 17-position in spinosyn D. It has only weak activity as an insecticide as the forosamine moiety is considered essential for potent activity. Synonyms: A 83543D pseudoaglycone; (2S, 3aR, 5aS, 5bS, 9S, 13S, 14R, 16aS, 16bS)-2-[(6-deoxy-2, 3, 4-tri-O-methyl-α-L-mannopyranosyl)oxy]-9-ethyl-2, 3, 3a, 5a, 5b, 6, 9, 10, 11, 12, 13, 14, 16a, 16b-tetradecahydro-13-hydroxy-4, 14-dimethyl-1H-as-indaceno[3, 2-d]oxacyclododecin-7, 15-dione. Grades: >95% by HPLC. CAS No. 131929-55-0. Molecular formula: C34H52O9. Mole weight: 604.77. | |
| Spinosyn D aglycone | It is an acid degradation product produced by hydrolysis of both saccharide groups on spinosyn D. It has only weak activity as an insecticide as the saccharides are considered essential for potent activity. Synonyms: A-83543D aglycone; (2S, 3aR, 5aS, 5bS, 9S, 13S, 14R, 16aS, 16bS)-9-ethyl-2, 3, 3a, 5a, 5b, 6, 9, 10, 11, 12, 13, 14, 16a, 16b-tetradecahydro-2, 13-dihydroxy-4, 14-dimethyl-1H-as-indaceno[3, 2-d]oxacyclododecin-7, 15-dione. Grades: >95% by HPLC. CAS No. 149439-79-2. Molecular formula: C25H36O5. Mole weight: 416.55. | |
| 3-Ethoxy-5,6-dihydro-spinosyn J 17-pseudoaglycone | It is an acid degradation product produced by selective hydrolysis of the more labile forosamine saccharide in the 17-position of 3-ethoxy-5,6-dihydrospinosyn J, the major component of the commercial product, spinetoram. It has only weak activity as an insecticide. Synonyms: 2-[(6-deoxy-3-O-ethyl-2, 4-di-O-methyl-α-L-mannopyranosyl)oxy]-9-ethyl-2R, 3, 3aR, 4, 5, 5aR, 5bS, 6, 9S, 10, 11, 12, 13S, 14R, 16aS, 16bR-hexadecahydro-13-hydroxy-14-methyl-1H-as-indaceno[3, 2-d]oxacyclododecin-7, 15-dione. Grades: >95% by HPLC. CAS No. 2055494-09-0. Molecular formula: C34H54O9. Mole weight: 606.79. | |
| 3-Ethoxy-spinosyn L 17-pseudoaglycone | It is an acid degradation product produced by selective hydrolysis of the more labile forosamine saccharide in the 17-position of 3-ethoxy-5,6-dihydrospinosyn J, the minor component of the commercial product, spinetoram. It has only weak activity as an insecticide. Grades: >95% by HPLC. Molecular formula: C35H54O9. Mole weight: 618.80. | |
| 3'-Ethoxy Spinosyn L 17-pseudoaglycone | 3'-Ethoxy spinosyn L 17-pseudoaglycone is an acid degradation product of 3'-ethoxy-5,6-dihydrospinosyn L which is a component of the insecticide spinosyn L. It has no insecticidal activity against the tobacco budworm up to a concentration of 64 ppm. 3'-Ethoxy spinosyn L 17-pseudoaglycone is only weakly active as an insecticide as the forosamine moiety is considered essential for potent activity. Grades: >95% by HPLC. Molecular formula: C35H54O9. Mole weight: 618.80. | |
| dTDP-4-amino-2,3,4,6-tetradeoxy-D-glucose N,N-dimethyltransferase | The enzyme was isolated from the bacterium Saccharopolyspora spinosa, where it is involved in the biosynthesis of spinosyn A, an active ingredient of several commercial insecticides. Group: Enzymes. Synonyms: SpnS; TDP-4-amino-2,3,6-trideoxy-D-glucose N,N-dimethyltransferase. Enzyme Commission Number: EC 2.1.1.324. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1932; dTDP-4-amino-2,3,4,6-tetradeoxy-D-glucose N,N-dimethyltransferase; EC 2.1.1.324; SpnS; TDP-4-amino-2,3,6-trideoxy-D-glucose N,N-dimethyltransferase. Cat No: EXWM-1932. |  |
| Spinetoram J | It is the major component in the second generation spinosyn family of bio-insecticides marketed as spinetoram. It is a semi-synthetic compound prepared by selective ethylation and hydrogenation of spinosyn J, and it is also an insecticide. Synonyms: 3-Ethoxy-5,6-dihydro-spinosyn J; XDE-175-J; [2R-(2R*, 3aR*, 5aR*, 5bS*, 9S*, 13S*, 14R*, 16aS*, 16bR*)]-2-[(6-Deoxy-3-O-ethyl-2, 4-di-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, 4, 5, 5a, 5b, 6, 9, 10, 11, 12, 13, 14, 16a, 16b-hexadecahydro-14-methyl-1H-as-Indaceno[3, 2-d]oxacyclododecin-7, 15-dione; (2R, 3aR, 5aR, 5bS, 9S, 13S, 14R, 16aS, 16bR)-2-[(6-Deoxy-3-O-ethyl-2, 4-di-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, 4, 5, 5a, 5b, 6, 9, 10, 11, 12, 13, 14, 16a, 16b-hexadecahydro-14-methyl-1H-as-indaceno[3, 2-d]oxacyclododecin-7, 15-dione. Grades: >95% by HPLC. CAS No. 187166-40-1. Molecular formula: C42H69NO10. Mole weight: 748.00. | |
| Spinetoram L | It is the minor component in the second generation spinosyn family of bio-insecticides marketed as spinetoram. It is a semi-synthetic compound prepared by selective ethylation and hydrogenation of spinosyn L, and it is also an insecticide. Synonyms: 3-Ethoxy-spinosyn L; 3'-O-Ethylspinosyn L; XDE 175L; (2S, 3aR, 5aS, 5bS, 9S, 13S, 14R, 16aS, 16bS)-2-[(6-Deoxy-3-O-ethyl-2, 4-di-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-4, 14-dimethyl-1H-as-indaceno[3, 2-d]oxacyclododecin-7, 15-dione. Grades: >95% by HPLC. CAS No. 187166-15-0. Molecular formula: C43H69NO10. Mole weight: 760.01. | |
| Spinosad | Spinosad, a mixture of spinosyns A and D known as fermentation products of a soil actinomycete ( Saccharopolyspora spinosa ), is a biological neurotoxic insecticide with a broader action spectrum. Spinosad targets the nicotinic acetylcholine receptor (nAChRs) of the insect nervous system. Spinosad has an excellent environmental and mammalian toxicological profile. Larvicidal activity [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 168316-95-8. Pack Sizes: 100 mg; 500 mg. Product ID: HY-138800. | |
| Spinosad | Spinosad is a broad-spectrum and naturally-occurring insecticide found in the the soil bacterium S. spinosa. Spinosad is a mixture of the macrocyclic lactones spinosyn A and spinosyn D , which act as agonists of insect nicotinic acetylcholinesterase receptors (nAChRs). Synonyms: Spinosyn A and D (mixture); Blackhawk; Comfortis; Conserve; Entrust; Entrust WP; Extinosad; GF 120; GF 120 Fruit Fly Bait; GF 120 NF Naturalyte; GF 120 Naturalyte Fruit Fly Bait; GF 1587; Gardens Alive Bulls-Eye; Laser; Laser (insecticide); Naturalure; Naturalure Fruit Fly Bait; Naturalyte; PP 105; SpinTor; Spinoace; Spinosad 45SC; Spinosad NT; Spinosyn A-spinosyn D mixt.; Success; Success 4; Success Naturalyte; Tracer; Tracer Naturalyte; Tracer Naturalyte Insect Control. Grades: ≥95%. CAS No. 168316-95-8. Molecular formula: C42H67NO10.C41H65NO10. Mole weight: 1477.94. | |
| Spinosad (A&D) | Spinosad is a broad spectrum insecticide and used as a reference standard. This compound is a mixture of Spinosyn A and Spinosyn D. Group: Biochemicals. Alternative Names: (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; Blackhawk; Comfortis; Conserve; Entrust; Entrust WP; Extinosad; GF 120; GF 120 Fruit Fly Bait; GF 120 NF Naturalyte; GF 120 Naturalyte Fruit Fly Bait; GF 1587; Gardens Alive Bulls-Eye; LY 232105; Laser; Laser (insecticide); Naturalure; Naturalure Fruit Fly Bait; Naturalyte; PP 105; SpinTor; Spinoace; Spinosad 45% SC; Spinosad 45SC; Spinosad NT; Spinosyn A-spinosyn D mixt.; Success; Success 4; Success Naturalyte; Tracer; Tracer Naturalyte; Tracer Naturalyte Insect Control; XDE 105. Grades: Highly Purified. CAS No. 168316-95-8. Pack Sizes: 5mg, 10mg, 25mg, 50mg. US Biological Life Sciences. | Worldwide |
| Spinosin | Spinosyn is a kind of effective C-saccharide, which has a protective effect. Spinosyn is active through Nrf2/HO-1 pathway inhibition Aβ 1-42 's production and combination [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 72063-39-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0651. | |
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