Tectoroside
Standard reference
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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
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.
Evid Based Complement Alternat Med.2017, 2017:9764843
Biosci Rep.2018, 38(4)
University of Burgos2024, ssrn.4795441.
J Pharm Biomed Anal.2022, 207:114398.
Int Immunopharmacol.2021, 101(Pt A):108181.
Oncotarget.2016, 8(51):88386-88400
Nat Commun.2019, 10(1):2745
Journal of Plant Growth Regulation2022, 10705-2.
Reprod Toxicol.2020, 96:1-10.
Current Topics in Nutraceutical Research2021, 19(1),p90-105.
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Zhongguo Zhong Yao Za Zhi. 2015 Oct;40(19):3800-4.
Chemical constituents from Crepis crocea.[Pubmed:
26975105]
METHODS AND RESULTS:
Thirteen compounds were isolated from the ethyl acetate fraction of Crepis crocea by column chromatographies on silica gel, Sephadex LH-20 and semi-preparative HPLC. The structures were elucidated on the basis of spectral analysis as tectorone I (1), 8β- (2-methyl- 2-hydroxy-3-oxobutanoyloxy) -glucozaluzanin C (2), Tectoroside (3), luteolin-7-O-glucoside (4), cosmosiin (5), esculetin (6), 3,4-dihydroxybenzaldehyde (7), trans-4-hydroxycinnamic acid (8), Caffeic acid (9), methyl p-hydroxyphenyllactate (10), ethylp- hydroxyphenyllactate (11), cis-3,4-dihydroxy-β-ionion (12).
CONCLUSIONS:
All the compounds, except for compounds 4 and 9, were isolated from this plant for the first time, and tectorone I (1) is a new natural product.
