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Junipediol A
Junipediol A
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Junipediol A
Price:
CAS No.: 86548-91-6
Catalog No.: CFN96603
Molecular Formula: C10H14O4
Molecular Weight: 198.22 g/mol
Purity: >=98%
Type of Compound: Phenylpropanoids
Physical Desc.: Powder
Source: The aerial parts of Juniperus phœnicea.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison
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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 / Inquiry
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Product Use Citation
Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: Junipediol A shows antioxidation activity.
In vitro:
Chinese Journal of Medicinal Chemistry, 2008,18 (3) :215-8.
Antioxidant phenylpropanoids from Cephalotaxus hainanensis.[Reference: WebLink]
To study the chemical constituents from Cephalotaxus hainanensis Li.
METHODS AND RESULTS:
The compounds were isolated and purified by column chromatography,and their structures were identified by physicochemical and spectral data.Their antioxidation activity were tested by DPPH method. Three compounds were isolated from the ethanol extract of Cephalotaxus hainanensis Li.,and their structures were elucidated as Junipediol A(1),Junipediol A 8-O-β-D-glucopyranoside(2),and junipediol B(3).
CONCLUSIONS:
Compounds 1-3 were isolated from the genus of Cephalotaxus for the first time,and all showed antioxidation activity.
Junipediol A Description
Source: The aerial parts of Juniperus phœnicea.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, 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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Cell. 2018 Jan 11;172(1-2):249-261.e12.
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IF=36.216(2019)

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Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
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Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.0449 mL 25.2245 mL 50.449 mL 100.898 mL 126.1225 mL
5 mM 1.009 mL 5.0449 mL 10.0898 mL 20.1796 mL 25.2245 mL
10 mM 0.5045 mL 2.5224 mL 5.0449 mL 10.0898 mL 12.6122 mL
50 mM 0.1009 mL 0.5045 mL 1.009 mL 2.018 mL 2.5224 mL
100 mM 0.0504 mL 0.2522 mL 0.5045 mL 1.009 mL 1.2612 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, 1997, 44(6):1169-73.
Three phenylpropanoids from Juniperus phœnicea.[Reference: WebLink]

METHODS AND RESULTS:
Three new compounds, Junipediol A [2-(3-methoxy-4-hydroxyphenyl)-propane-1,3-diol], Junipediol A 8-glucoside [1-β-d-glucosyloxy-2-(3-methoxy-4-hydroxyphenyl)-propane-1,3-diol] and junipediol B 8-glucoside [1-β-d-glucosyloxy-2-(3,4-methylenedioxyphenyl)-propane-1,3-diol], have been isolated from acetone and methanolic extracts of the aerial parts of Juniperus phœnicea.
CONCLUSIONS:
The structural elucidation of these new natural products was achieved mainly by UV, mass and 1H and 13C NMR spectroscopy.
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