Neoolivil

CAS# 1277182-38-3

Neoolivil

Catalog No. BCX0193----Order now to get a substantial discount!

Product Name & Size Price Stock
Neoolivil: 5mg $903 In Stock
Neoolivil: 10mg Please Inquire In Stock
Neoolivil: 20mg Please Inquire Please Inquire
Neoolivil: 50mg Please Inquire Please Inquire
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Neoolivil: 200mg Please Inquire Please Inquire
Neoolivil: 500mg Please Inquire Please Inquire
Neoolivil: 1000mg Please Inquire Please Inquire

Quality Control of Neoolivil

Number of papers citing our products

Chemical structure

Neoolivil

Chemical Properties of Neoolivil

Cas No. 1277182-38-3 SDF Download SDF
PubChem ID N/A Appearance Powder
Formula C20H24O7 M.Wt 376.44
Type of Compound Lignans Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Neoolivil Dilution Calculator

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Neoolivil Molarity Calculator

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Preparing Stock Solutions of Neoolivil

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.6565 mL 13.2823 mL 26.5647 mL 53.1293 mL 66.4116 mL
5 mM 0.5313 mL 2.6565 mL 5.3129 mL 10.6259 mL 13.2823 mL
10 mM 0.2656 mL 1.3282 mL 2.6565 mL 5.3129 mL 6.6412 mL
50 mM 0.0531 mL 0.2656 mL 0.5313 mL 1.0626 mL 1.3282 mL
100 mM 0.0266 mL 0.1328 mL 0.2656 mL 0.5313 mL 0.6641 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on Neoolivil

[Lignans from barks of Ailanthus altissima].[Pubmed:28936846]

Zhongguo Zhong Yao Za Zhi. 2016 Dec;41(24):4615-4620.

Eleven lignans were isolated from the ethanol extract of the barks of Ailanthus altissima through various column chromatography methods including silica gel, Sephadex LH-20, ODS and HPLC. By physical, chemical and comprehensive spectroscopic methods, their structures were identified as (+)-Neoolivil(1), prunustosanan AI (2), (7S,8R)-guaiacyl-glycerol-beta-O-4'-neolignan (3), (7R,8S)-guaiacyl-glycerol-beta-O-4'-neolignan (4), (7S,8R)-1-(4-hydroxy-3-methoxyphenyl)-2-[4-(3-hydroxypropyl)-2,6-dimethoxyphenoxy]-1,3-propanediol(5), pinnatifidanin B V (6), pinnatifidanin B VI (7), (7R,7'R,7''S,8S,8'S,8''S)-4',4''-dihydroxy-3,3',3'',5-tetramethoxy-7,9':7',9-diepoxy-4,8''-oxy-8,8'-sesquineolignan-7'',9''-diol (8), hedyotol D (9), 5-(2-propenyl)-7-methoxy-2-(3,4-methylenediovxyphenyl)benzofuran (10), and (7R,8S,7'E)-guaiacyl-glycerol-beta-O-4'-sinapyl ether(11).All of these compounds were isolated from this plant for the first time.

Lignans from the roots of Urtica dioica and their metabolites bind to human sex hormone binding globulin (SHBG).[Pubmed:9434605]

Planta Med. 1997 Dec;63(6):529-32.

Polar extracts of the stinging nettle (Urtica dioica L.) roots contain the ligans (+)-Neoolivil, (-)-secoisolariciresinol, dehydrodiconiferyl alcohol, isolariciresinol, pinoresinol, and 3,4-divanillyltetrahydrofuran. These compounds were either isolated from Urtica roots, or obtained semisynthetically. Their affinity to human sex hormone binding globulin (SHBG) was tested in an in vitro assay. In addition, the main intestinal transformation products of plant lignans in humans, enterodiol and enterolactone, together with enterofuran were checked for their activity. All lignans except (-)-pinoresinol developed a binding affinity to SHBG in the in vitro assay. The affinity of (-)-3,4-divanillyltetrahydrofuran was outstandingly high. These findings are discussed with respect to potential beneficial effects of plant lignans on benign prostatic hyperplasia (BPH).

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