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| Product | Description | |
|---|---|---|
| Ginsenoside F1 | Ginsenoside F1, a metabolite of ginsenoside Rg1, is reported to be antiaging and antioxidative, and to have beneficial effects on skin. It significantly reduced ultraviolet-B-induced cell death and protected HaCaT cells from apoptosis caused by ultraviolet B irradiation. Uses: A metabolite of ginsenoside rg1. Synonyms: (20S)-20-(β-D-Glucopyranosyloxy)dammar-24-ene-3β,6α,12β-triol; 3β,6α,12β-Trihydroxy-5α-dammar-24-en-20-yl β-D-glucopyranoside; (3b,6a,12b)-3,6,12-Trihydroxydammar-24-ene-20-yl beta-D-glucopyranoside; 20(S)-Ginsenoside F1; Panaxoside Aprogenin. Grade: >98%. CAS No. 53963-43-2. Molecular formula: C36H62O9. Mole weight: 638.87. |  |
| Ginsenoside F1 | Ginsenoside F1, an enzymatically modified derivative of Ginsenoside Rg1, demonstrates competitive inhibition of CYP3A4 activity and weaker inhibition of CYP2D6 activity. Uses: Scientific research. Group: Natural products. Alternative Names: 20(S)-Ginsenoside F1. CAS No. 53963-43-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg. Product ID: HY-N0598. |  |
| Ginsenoside F1 | Ginsenoside F1. Group: Biochemicals. Grades: Plant Grade. CAS No. 53963-43-2. Pack Sizes: 20mg. Molecular Formula: C36H62O9, Molecular Weight: 638.87. US Biological Life Sciences. |  Worldwide |
| Ginsenoside F1 | Ginsenoside F1. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3β,6α,12β-Trihydroxy-5α-dammar-24-en-20-yl β-D-glucopyranoside. Appearance: White powder. CAS No. 53963-43-2. Molecular formula: C36H62O9. Mole weight: 638.87. Purity: 0.98. IUPACName: (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(2S)-6-methyl-2-[(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,6,12-trihydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]hept-5-en-2-yl]oxyoxane-3,4,5-triol. Canonical SMILES: CC(=CCC[C@@](C)([C@H]1CC[C@@]2([C@@H]1[C@@H](C[C@H]3[C@]2(C[C@@H]([C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)O)C)O)C)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)C. Density: 1.23±0.1 g/ml. Product ID: ACM53963432. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 20(S)-Ginsenoside F1 | Ginsenoside F1 is a bioactive metabolite of the ginsenoside component of Panax ginseng with the ability to inhibit human cytochrome P450 enzymes. This has application in anti-cancer therapeutics as well as protective liver effects. Group: Biochemicals. Grades: Highly Purified. CAS No. 53963-43-2. Pack Sizes: 10mg, 25 mg. Molecular Formula: C36H62O9. US Biological Life Sciences. | Worldwide |
| Pseudoginsenoside F11 | Pseudoginsenoside F11 (Ginsenoside A1), a component of Panax quinquefolium (American ginseng), has been demonstrated to antagonize the learning and memory deficits induced by scopolamine, morphine and methamphetamine in mice. Uses: Scientific research. Group: Natural products. Alternative Names: Ginsenoside A1. CAS No. 69884-00-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-N0541. | |
| Pseudoginsenoside F11 | Pseudoginsenoside F11. Group: Biochemicals. Alternative Names: Ginsenoside A1. Grades: Plant Grade. CAS No. 69884-00-0. Pack Sizes: 20mg. Molecular Formula: C42H72O14, Molecular Weight: 801.013. US Biological Life Sciences. | Worldwide |
| Pseudoginsenoside-F11 | Pseudoginsenoside-F11 is extracted from the roots of Panax ginseng C. A. Mey. It antagonized the memory dysfunction induced by scopolamine. It has been shown to antagonize the behavioral actions of morphine. It may block the development of morphine-induced behavioral sensitization via its effect, at least partially, on the glutamatergic system in the medial prefrontal cortex (mPFC). Uses: An oxotillol-type ginsenoside which displayes neuroprotective activity. Synonyms: (20S,24R)-6α-(2-O-α-L-Rhamnopyranosyl-β-D-glucopyranosyloxy)-20,24-epoxy-5α-dammarane-3β,12β,25-triol; (24R)-Pseudoginsenoside F11; [(24R)-20,24-Epoxy-3β,12β,25-trihydroxy-5α-dammaran-6α-yl] 2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside; Pseudoginsenoside F11; 17β-[[(2S)-2β-Methyl-5α-(1-hydroxy-1-methylethyl)tetrahydrofuran]-2-yl]-3β,12β-dihydroxy-4,4,8β,10β,14α-pentamethyl-5α-gonane-6α-yl 2-O-α-L-rhamnopyranosyl-β-D-glucopyranoside; Ginsenoside A1; (3β,6α,12β,24R)-20,24-Epoxy-3,12,25-trihydroxydammaran-6-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside; 24(R)-Pseudoginsenoside F11. Grade: >98%. CAS No. 69884-00-0. Molecular formula: C42H72O14. Mole weight: 801.01. | |
| ginsenosidase type IV | Ginsenosidase type IV catalyses the sequential hydrolysis of the 6-O-β-D-(1?2)-glycosidic bond or the 6-O-α-D-(1?2)-glycosidic bond in protopanaxatriol-type ginsenosides with a disacchride attached to the C6 position, followed by the hydrolysis of the remaining 6-O-β-D-glycosidic bond (e.g. ginsenoside Re ? ginsenoside Rg1 ? ginsenoside F1). Group: Enzymes. Enzyme Commission Number: EC 3.2.1.194. 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-3878; ginsenosidase type IV; EC 3.2.1.194. Cat No: EXWM-3878. |  |
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