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| Product | Description | |
|---|---|---|
| 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. Grade: >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. Grade: >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. Grade: >95% by HPLC. Molecular formula: C35H54O9. Mole weight: 618.80. | |
| dTDP-3,4-didehydro-2,6-dideoxy-α-D-glucose 3-reductase | The enzyme is involved in the biosynthesis of several deoxysugars, including L-digitoxose, L- and D-olivose, L-oliose, D-mycarose and forosamine. |  |
| dTDP-3,4-didehydro-2,6-dideoxy-α-D-glucose 3-reductase | The enzyme is involved in the biosynthesis of several deoxysugars, including L-digitoxose, L- and D-olivose, L-oliose, D-mycarose and forosamine. Group: Enzymes. Synonyms: KijD10; dTDP-4-keto-2,6-dideoxy-D-glucose 3-oxidoreductase; dTDP-4-dehydro-2,6-dideoxy-α-D-glucose 3-oxidoreductase. Enzyme Commission Number: EC 1.1.1.384. 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-0303; dTDP-3,4-didehydro-2,6-dideoxy-α-D-glucose 3-reductase; EC 1.1.1.384; KijD10; dTDP-4-keto-2,6-dideoxy-D-glucose 3-oxidoreductase; dTDP-4-dehydro-2,6-dideoxy-α-D-glucose 3-oxidoreductase. Cat No: EXWM-0303. | |
| dTDP-4-dehydro-2,3,6-trideoxy-D-glucose 4-aminotransferase | A pyridoxal-phosphate protein. The enzyme, isolated from the bacterium Saccharopolyspora spinosa, participates in the biosynthesis of forosamine. Group: Enzymes. Synonyms: SpnR; TDP-4-keto-2,3,6-trideoxy-D-glucose 4-aminotransferase. Enzyme Commission Number: EC 2.6.1.110. 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-2851; dTDP-4-dehydro-2,3,6-trideoxy-D-glucose 4-aminotransferase; EC 2.6.1.110; SpnR; TDP-4-keto-2,3,6-trideoxy-D-glucose 4-aminotransferase. Cat No: EXWM-2851. | |
| dTDP-4-dehydro-2,6-dideoxy-D-glucose 3-dehydratase | A pyridoxal 5'-phosphate protein. The enzyme, isolated from the bacterium Saccharopolyspora spinosa, participates in the biosynthesis of forosamine. Requires ferredoxin/ferredoxin reductase or flavodoxin/flavodoxin reductase. Group: Enzymes. Synonyms: SpnQ; TDP-4-keto-2,6-dideoxy-D-glucose 3-dehydrase. Enzyme Commission Number: EC 4.2.1.164. 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-5005; dTDP-4-dehydro-2,6-dideoxy-D-glucose 3-dehydratase; EC 4.2.1.164; SpnQ; TDP-4-keto-2,6-dideoxy-D-glucose 3-dehydrase. Cat No: EXWM-5005. | |
| dTDP-4-dehydro-6-deoxy-α-D-glucopyranose 2,3-dehydratase | The enzyme participates in the biosynthesis of several deoxysugars, including β-L-4-epi-vancosamine, α-L-megosamine, L- and D-olivose, D-oliose, D-mycarose, forosamine and β-L-digitoxose. In vitro the intermediate can undergo a spontaneous decomposition to maltol. | |
| dTDP-4-dehydro-6-deoxy-α-D-glucopyranose 2,3-dehydratase | The enzyme participates in the biosynthesis of several deoxysugars, including β-L-4-epi-vancosamine, α-L-megosamine, L- and D-olivose, D-oliose, D-mycarose, forosamine and β-L-digitoxose. In vitro the intermediate can undergo a spontaneous decomposition to maltol. Group: Enzymes. Synonyms: jadO (gene name); evaA (gene name); megBVI (gene name); eryBV (gene name); mtmV (gene name); oleV (gene name); spnO (gene name); TDP-4-keto-6-deoxy-D-glucose 2,3-dehydratase; dTDP-4-dehydro-6-deoxy-α-D-glucopyranose hydro-lyase (dTDP-(2R,6S)-2,4-dihydroxy-6-methyl-2,6-dihydropyran-3-one-forming). Enzyme Commission Number: EC 4.2.1.159. 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-5000; dTDP-4-dehydro-6-deoxy-α-D-glucopyranose 2,3-dehydratase; EC 4.2.1.159; jadO (gene name); evaA (gene name); megBVI (gene name); eryBV (gene name); mtmV (gene name); oleV (gene name); spnO (gene name); TDP-4-keto-6-deoxy-D-glucose 2,3-dehydratase; dTDP-4-dehydro-6-deoxy-α-D-glucopyranose hydro-lyase (dTDP-(2R,6S)-2,4-dihydroxy-6-methyl-2,6-dihydropyran-3-one-forming). Cat No: EXWM-5000. | |
| 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. Grade: >95% by HPLC. CAS No. 131929-68-5. Molecular formula: C33H50O9. Mole weight: 590.74. | |
| 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. Grade: >95% by HPLC. CAS No. 131929-55-0. Molecular formula: C34H52O9. Mole weight: 604.77. | |
| Spiramycin | Spiramycin (Rovamycin) is a macrolide antibiotic produced by Streptomyces ambofaciens with against bacteria and Toxoplasma gondii activities, and also has antiparasitic effect. Spiramycin is composed of a 16-member lactone ring, on which three sugars (mycaminose, forosamine, and mycarose) are attached [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Rovamycin. CAS No. 8025-81-8. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-100593. |  |
| 3'-O-Forosaminyl-griseusin A | Produced by the strain of Streptomyces griseus MJ361-48F3, it showed activity against gram-positive bacteria including methicillin-resistant Staphylococcus aureus (MRSA) with MIC of 0.39-1.56 μg/mL. Synonyms: 3'-O-alpha-D-Forosaminyl-(+)-griseusin A; OF-griseusin A. CAS No. 158268-23-6. Molecular formula: C30H35NO11. Mole weight: 585.60. | |
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