| Size | Price | |
|---|---|---|
| 500mg | ||
| 1g | ||
| Other Sizes |
| Targets |
ERK; p38 MAPK; JAK2; STAT3; IL-1β; IL-6; COX-2; IL-10
|
|---|---|
| ln Vitro |
LPS (lipopolysaccharide)-stimulated phosphorylated ERK and p38 MAPK are inhibited by broussonin E (20 μM, 3 h)[1]. Janus regulatory (JAK) 2 and signal transducer and activator of transcription (STAT) 3 are activated by broussonin E [1]. In RAW264.7 cells, broussonin E (0–20 μM, 3 h) can suppress the production of pro-inflammatory mediators such as TNF-α, IL-1β, IL-6, COX-2, and iNOS that are stimulated by LPS[1]. In LPS-stimulated RAW264.7 cells, broussonin E increases the production of anti-inflammatory mediators like IL-10, CD206, and arginase-1 (Arg-1) [1].
|
| Cell Assay |
Western Blot Analysis[1]
Cell Types: RAW264.7 cells Tested Concentrations: 2.5, 5, 10 and 20 Incubation Duration: 3 hrs (hours) Experimental Results: Inhibition of p-ERK and p-p38 MAPK in LPS stimulated RAW264.7 cells, but not Inhibit p-JNK MAPK expression. |
| References | |
| Additional Infomation |
broussonin E has been reported in Broussonetia papyrifera with data available.
|
| Molecular Formula |
C17H20O4
|
|---|---|
| Molecular Weight |
288.338305473328
|
| Exact Mass |
288.136
|
| CAS # |
90902-21-9
|
| Related CAS # |
90902-21-9
|
| PubChem CID |
14213544
|
| Appearance |
White to off-white solid
|
| Density |
1.2±0.1 g/cm3
|
| Boiling Point |
464.9±40.0 °C at 760 mmHg
|
| Flash Point |
235.0±27.3 °C
|
| Vapour Pressure |
0.0±1.2 mmHg at 25°C
|
| Index of Refraction |
1.586
|
| LogP |
3.35
|
| Hydrogen Bond Donor Count |
2
|
| Hydrogen Bond Acceptor Count |
4
|
| Rotatable Bond Count |
6
|
| Heavy Atom Count |
21
|
| Complexity |
297
|
| Defined Atom Stereocenter Count |
0
|
| SMILES |
OC1C(OC)=CC=C(CCCC2C(O)=CC(OC)=CC=2)C=1
|
| InChi Key |
GDCSYNUJDYRGRF-UHFFFAOYSA-N
|
| InChi Code |
InChI=1S/C17H20O4/c1-20-14-8-7-13(15(18)11-14)5-3-4-12-6-9-17(21-2)16(19)10-12/h6-11,18-19H,3-5H2,1-2H3
|
| Chemical Name |
5-[3-(2-hydroxy-4-methoxyphenyl)propyl]-2-methoxyphenol
|
| Synonyms |
Broussonin E
|
| HS Tariff Code |
2934.99.9001
|
| Storage |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
| Shipping Condition |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
|
| Solubility (In Vitro) |
DMSO: ~100 mg/mL (~346.8 mM)
|
|---|---|
| Solubility (In Vivo) |
Solubility in Formulation 1: ≥ 2.5 mg/mL (8.67 mM) (saturation unknown) in 10% DMSO + 40% PEG300 + 5% Tween80 + 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 25.0 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. Solubility in Formulation 2: ≥ 2.5 mg/mL (8.67 mM) (saturation unknown) in 10% DMSO + 90% (20% SBE-β-CD in 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 25.0 mg/mL clear DMSO stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly. Preparation of 20% SBE-β-CD in Saline (4°C，1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution. View More
Solubility in Formulation 3: ≥ 2.5 mg/mL (8.67 mM) (saturation unknown) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), clear solution. |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 3.4681 mL | 17.3406 mL | 34.6813 mL | |
| 5 mM | 0.6936 mL | 3.4681 mL | 6.9363 mL | |
| 10 mM | 0.3468 mL | 1.7341 mL | 3.4681 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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