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    Natural Products
    Pseudoginsenoside RT1
    Information
    CAS No. 98474-74-9 Price $338 / 20mg
    Catalog No.CFN90656Purity>=98%
    Molecular Weight927.1Type of CompoundTriterpenoids
    FormulaC47H74O18Physical DescriptionPowder
    Download     COA    MSDS    SDFSimilar structuralComparison (Web)  (SDF)
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    According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
    Size /Price /Stock 10 mM * 1 mL in DMSO / $219.7 / In-stock
    Other Packaging *Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap
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    Pseudoginsenoside RT1

    Pseudoginsenoside RT1
    Product Name Pseudoginsenoside RT1
    CAS No.: 98474-74-9
    Catalog No.: CFN90656
    Molecular Formula: C47H74O18
    Molecular Weight: 927.1 g/mol
    Purity: >=98%
    Type of Compound: Triterpenoids
    Physical Desc.: Powder
    Source: The roots of Panax ginseng C. A. Mey.
    Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
    Price: $338 / 20mg
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    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
    10 mM * 1 mL in DMSO / Inquiry / In-stock
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  • Biological Activity
    Description: Pseudoginsenoside RT1 can cause a decrease in blood pressure, an increase in heart rate and an increase in spontaneous contractility of the uterus.
    In vivo:
    Pharmaceutical Biology, 2008 ,37 (1) :42-45.
    Biological Activity of Crude Extract and Saponin Pseudoginsenoside-RT1 Derived from the Fruit of Randia siamensis[Reference: WebLink]

    METHODS AND RESULTS:
    Ursolic acid (1), pseudoginsenoside-RP 1 (2), and Pseudoginsenoside RT1 (3) were isolated from the fruit of Randia siamensis. 13 C NMR spectroscopy was particularly useful in confirming the structures of these components. Studies with rats showed that saponin 3 caused a decrease in blood pressure, an increase in heart rate and an increase in spontaneous contractility of the uterus.
    CONCLUSIONS:
    Also, a crude ethanol extract of the fruit of R. siamensis exhibited acute ichthyotoxic activity.
    Pseudoginsenoside RT1 Description
    Source: The roots of Panax ginseng C. A. Mey.
    Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
    Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

    After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.0786 mL 5.3932 mL 10.7863 mL 21.5726 mL 26.9658 mL
    5 mM 0.2157 mL 1.0786 mL 2.1573 mL 4.3145 mL 5.3932 mL
    10 mM 0.1079 mL 0.5393 mL 1.0786 mL 2.1573 mL 2.6966 mL
    50 mM 0.0216 mL 0.1079 mL 0.2157 mL 0.4315 mL 0.5393 mL
    100 mM 0.0108 mL 0.0539 mL 0.1079 mL 0.2157 mL 0.2697 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    Protocol
    Structure Identification:
    Phytochemistry. 1994 Mar 30;35(5):1319-24.
    Oleanolic acid saponins from root bark of Aralia elata.[Pubmed: 7764823]
    Three new oleanolic acid glycosides, tarasaponins I-III, were isolated as their methyl esters from the root bark of Aralia elata together with four known glycosides, the methyl esters of chikusetsusaponins IVa, IV, 28-desglucosyl-chikusetsusaponin IV and Pseudoginsenoside RT1.
    METHODS AND RESULTS:
    Tarasaponins I-III were characterized as oleanolic acid 3-O-[beta-D-glucopyranosyl(1-->3)][alpha-L-arabinofuranosyl(1-->4)[- beta-D-glucuronopyranoside, oleanolic acid 3-O-[beta-D-xylopyranosyl(1-->2)][beta-D-galactopyranosyl(1-->3)]-beta- D-glucuronopyranoside and beta-D-glucopyranosyl oleanolate 3-O-beta-D-galactopyranosyl(1-->3)-beta-D-glucuronopyranoside, respectively.
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