|Source:||The roots of Lithosperraum erythrorhizon Sieb. et Zucc.|
|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: firstname.lastname@example.org
|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.|
|1 mg||5 mg||10 mg||20 mg||25 mg|
|1 mM||2.3229 mL||11.6144 mL||23.2288 mL||46.4576 mL||58.072 mL|
|5 mM||0.4646 mL||2.3229 mL||4.6458 mL||9.2915 mL||11.6144 mL|
|10 mM||0.2323 mL||1.1614 mL||2.3229 mL||4.6458 mL||5.8072 mL|
|50 mM||0.0465 mL||0.2323 mL||0.4646 mL||0.9292 mL||1.1614 mL|
|100 mM||0.0232 mL||0.1161 mL||0.2323 mL||0.4646 mL||0.5807 mL|
Natural Product Research, 2015, Mar 26,30(5):574-577.
|Anti-skin ageing activity of napthoquinones from Arnebia nobilis Reichb.f.[Pubmed: 25810219]|
|The present isolation and identification of napthoquinones from roots of Arnebia nobilis Reichb.f. can lead to the discovery of new anti-skin ageing ingredient in colour cosmetics. Four compounds have been isolated and purified by rigorous column chromatography. The compounds are identified as β, β-dimethylacryl alkannin (AN-I), Acetoxyisovalerylalkannin (AAN-II), acetyl alkannin (AN-III) and alkannin (AN-IV) by interpretation of spectroscopic data. This study is the first to report the isolation of Acetoxyisovaleryl alkannin (AAN-II) from A. nobilis. The IC50 values of the compounds, determined in human skin cells (human dermal fibroblasts and human keratinocytes) and mouse embryonic fibroblasts (NIH3T3) varied significantly among the four alkannins. Among the four compounds, β-acetoxyisovaleryl alkannin (AAN-II) significantly inhibited hydrogen peroxide (H2O2)-induced red blood corpuscle haemolysis and cellular senescence in human dermal fibroblasts. Collagen-I, elastin and involucrin syntheses in human dermal fibroblasts or keratinocytes were up regulated by AAN-II. These results support the potential utility of alkannins as novel anti-ageing ingredients.|
Journal of Jilin University, 2010 , 48 (2) :319-322.
|Chemical Constituents from Root of Arnebia euchroma(Royle)Johnst[Reference: WebLink]|
|All the compounds were separated from the petroleum ether extracts of Arnebia euchroma root by means of column chromatography and their structures were identified by the spectral analysis and chemical evidence.Seven compounds were separated and identified as deoxyshikonin (1),β,β-dimethylacryloylshikonin (2),acetyshikonin (3),shikonin (4),β-sitosterol (5),propionylshikonin (6),Acetoxyisovalerylalkannin (7).|