| Size | Price | Stock | Qty |
|---|---|---|---|
| 1mg |
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| 5mg |
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| 10mg |
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| Other Sizes |
| Targets |
Torachrysone-8-O-β-D-glucoside does not have a defined biological target. It exhibits antioxidant and anti-inflammatory activities. It may modulate signaling pathways involved in inflammation and oxidative stress. It is a naphthalene glycoside from Rheum palmatum.
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|---|---|
| ln Vitro |
In vitro, torachrysone-8-O-β-D-glucoside exhibits antioxidant activity by scavenging free radicals. It may also show anti-inflammatory activity by inhibiting the production of pro-inflammatory mediators. It is used in research to study the pharmacological properties of rhubarb compounds.
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| ln Vivo |
Torachrysone-8-O-β-D-glucoside is not a pharmacologically approved drug. It is a natural product and research compound with antioxidant and anti-inflammatory activities. It has not been evaluated in clinical trials.
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| Enzyme Assay |
In vitro assays for torachrysone-8-O-β-D-glucoside typically involve antioxidant and anti-inflammatory activity measurements. A standard protocol for antioxidant activity involves incubating the compound with DPPH or ABTS radicals and measuring the reduction in absorbance. For anti-inflammatory activity, cells are treated with the compound and stimulated with LPS, and cytokine production is measured.
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| Cell Assay |
In vitro cell culture experiments with torachrysone-8-O-β-D-glucoside typically involve immune cells or other cell types. Cells are cultured in appropriate media and treated with the compound at concentrations ranging from 1-100 µM for 24 hours. Antioxidant and anti-inflammatory markers are measured.
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| Animal Protocol |
In vivo animal studies with torachrysone-8-O-β-D-glucoside are not well documented. It is used primarily as a research compound.
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| ADME/Pharmacokinetics |
Pharmacokinetic properties of torachrysone-8-O-β-D-glucoside are not characterized, as it is not a drug substance. The compound is not intended for human exposure.
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| Toxicity/Toxicokinetics |
Torachrysone-8-O-β-D-glucoside may cause skin and eye irritation. Standard laboratory safety precautions should be followed when handling this compound, including the use of gloves, safety glasses, and working in a fume hood.
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| References | |
| Additional Infomation |
Torachrysone 8-O-glucoside has been reported in Rumex acetosa, Rumex japonicus, and other organisms with available data.
Torachrysone-8-O-β-D-glucoside is a naphthalene glycoside from Rheum palmatum with antioxidant and anti-inflammatory properties. It has not undergone clinical trials and is not approved as a pharmaceutical. |
| Molecular Formula |
C20H24O9
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|---|---|
| Molecular Weight |
408.40
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| Exact Mass |
408.142
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| CAS # |
64032-49-1
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| PubChem CID |
11972479
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| Appearance |
Light yellow to yellow solid
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| Density |
1.5±0.1 g/cm3
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| Boiling Point |
676.9±55.0 °C at 760 mmHg
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| Melting Point |
150 - 152 °C
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| Flash Point |
239.8±25.0 °C
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| Vapour Pressure |
0.0±2.2 mmHg at 25°C
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| Index of Refraction |
1.656
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| LogP |
0.71
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| Hydrogen Bond Donor Count |
5
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| Hydrogen Bond Acceptor Count |
9
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| Rotatable Bond Count |
5
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| Heavy Atom Count |
29
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| Complexity |
572
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| Defined Atom Stereocenter Count |
5
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| SMILES |
CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)OC
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| InChi Key |
GHKWPHRULCFTBB-CZNQJBLBSA-N
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| InChi Code |
InChI=1S/C20H24O9/c1-8-4-10-5-11(27-3)6-12(15(10)17(24)14(8)9(2)22)28-20-19(26)18(25)16(23)13(7-21)29-20/h4-6,13,16,18-21,23-26H,7H2,1-3H3/t13-,16-,18+,19-,20-/m1/s1
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| Chemical Name |
1-[1-hydroxy-6-methoxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone
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| Synonyms |
Torachrysone-8-O-b-D-glucoside
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| HS Tariff Code |
2934.99.9001
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| Storage |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month Note: Please store this product in a sealed and protected environment (e.g. under nitrogen), avoid exposure to moisture and light. |
| Shipping Condition |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
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| Solubility (In Vitro) |
DMSO: 50 mg/mL (122.43 mM)
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|---|---|
| Solubility (In Vivo) |
Solubility in Formulation 1: ≥ 1.25 mg/mL (3.06 mM) (saturation unknown) in 10% DMSO + 40% PEG300 +5% Tween-80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 12.5 mg/mL clear DMSO stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 + to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL. Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution. (Please use freshly prepared in vivo formulations for optimal results.) |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 2.4486 mL | 12.2429 mL | 24.4858 mL | |
| 5 mM | 0.4897 mL | 2.4486 mL | 4.8972 mL | |
| 10 mM | 0.2449 mL | 1.2243 mL | 2.4486 mL |
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.
Calculation results
Working concentration： mg/mL；
Method for preparing DMSO stock solution： mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation:：Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O，mix and clarify.
(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
(2) Be sure to add the solvent(s) in order.
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