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| Product | Description | |
|---|---|---|
| Protopanaxatriol | 20S-Protopanaxatriol (g-PPT), a dammarane-type tetracyclic terpene sapogenin, may be used to study its binding to and modulation of cell function via glucocortoid (GR) and oestrogen (ER) receptors. Protopanaxatriol can be used in health products. Synonyms: 20(S)-APPT; g-PPT. Grade: >98%. CAS No. 34080-08-5. Molecular formula: C30H52O4. Mole weight: 476.73. |  |
| Protopanaxatriol | Botanical Source: Group: Biochemicals. Alternative Names: (20R)-Protopanaxatriol. Grades: Plant Grade. CAS No. 1453-93-6. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| Protopanaxatriol, 20S- | Protopanaxatriol, 20S-. Group: Biochemicals. CAS No. 34080-08-5. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| 20(s)-Protopanaxatriol | 20(s)-Protopanaxatriol. Group: Biochemicals. Grades: Plant Grade. CAS No. 34080-08-5. Pack Sizes: 20mg. Molecular Formula: C30H52O4, Molecular Weight: 476.73. US Biological Life Sciences. | Worldwide |
| (20S)-Protopanaxatriol | (20S)-Protopanaxatriol acts as an inhibitor in the production of corticosteroids in fasciculata cells. Used in the clinical treatment of heart diseases. Group: Biochemicals. Grades: Highly Purified. CAS No. 34080-08-5. Pack Sizes: 25mg, 50mg. Molecular Formula: C30H52O4, Molecular Weight: 476.73. US Biological Life Sciences. | Worldwide |
| (20S)-Protopanaxatriol | (20S)-Protopanaxatriol is a metabolite of ginsenoside. (20S)-Protopanaxatriol works through the glucocorticoid receptor (GR) and estrogen receptor (ER) , and is also a LXRα inhibitor. (20 S )-Protopanaxatriol shows a broad spectrum of antitumor effects [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: 20(S)-APPT; g-PPT. CAS No. 34080-08-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0835. |  |
| 20S-Protopanaxatriol | 20S-Protopanaxatriol. Group: Biochemicals. Alternative Names: g-PPT. Grades: Highly Purified. CAS No. 34080-08-5. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C30H52O4. US Biological Life Sciences. | Worldwide |
| 20(S),24(R)-Ocotillol | 20(S),24(R)-Ocotillol. Group: Biochemicals. Alternative Names: 20(S)-protopanaxatriol oxide I. Grades: Plant Grade. CAS No. 69926-31-4. Pack Sizes: 5mg. Molecular Formula: C30H52O5, Molecular Weight: 492.741. US Biological Life Sciences. | Worldwide |
| 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. |  |
| protopanaxadiol 6-hydroxylase | A heme-thiolate protein (P-450). Involved in the biosynthetic pathway of ginsenosides. Isolated from the rhizomes of ginseng (Panax ginseng). Group: Enzymes. Synonyms: protopanaxatriol synthase; P6H; CYP716A53v2; protopanaxadiol,NADPH:O2 oxidoreductase (6α-hydroxylating). Enzyme Commission Number: EC 1.14.13.184. 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-0783; protopanaxadiol 6-hydroxylase; EC 1.14.13.184; protopanaxatriol synthase; P6H; CYP716A53v2; protopanaxadiol,NADPH:O2 oxidoreductase (6α-hydroxylating). Cat No: EXWM-0783. | |
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