Cosmosiin - CAS 578-74-5
Catalog number: B0005-094880
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Molecular Formula:
C21H20O10
Molecular Weight:
432.4
COA:
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Chemical Family:
Flavonoids
Description:
Cosmosiin also called Apigenin 7-O-glucoside, is a natural flavonoid found in the flowers of Cosmos bipinnatus. Cosmosiin exhibits the activities of anti-HIV, anti-proliferative and antioxidant, the compound may be beneficial for diabetic complications through their enhanced adiponectin secretion, tyrosine phosphorylation of insulin receptor-β and GLUT4 translocation.
Ordering Information
Catalog Number Size Price Stock Quantity
B0005-094880 20mg $479 In stock
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Purity:
>98%
Appearance:
Yellow powder
Synonyms:
Apigenin 7-O-glucoside
MSDS:
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Application:
anti-proliferative; antioxidant; anti-HIV
Quality Standard:
Enterprise Standard
Quantity:
Milligrams-Grams
Density:
1.642g/cm3
1.Analysis of the erythroid differentiation effect of flavonoid apigenin on K562 human chronic leukemia cells.
Isoda H;Motojima H;Onaga S;Samet I;Villareal MO;Han J Chem Biol Interact. 2014 Sep 5;220:269-77. doi: 10.1016/j.cbi.2014.07.006. Epub 2014 Jul 21.
The erythroid differentiation-inducing effect of apigenin and its derivatives on human chronic myeloid leukemia K562 has been reported but the functional group in its structure responsible for the effect has not yet been elucidated. Here, we determined the moiety responsible for the erythroid differentiation induction effect of apigenin by using different flavonoids to represent the functional groups in its structure. In addition, we compared apigenin and apigetrin, a flavonoid similar in structure to apigenin except for the glycoside in its structure. Morphological changes as well as expressions of specific markers in K562 cells treated with apigenin were compared with those treated with apigetrin, flavone, 7-hydroxyflavone, chrysin, luteolin, or naringenin. The anti-proliferative and erythroid differentiation-inducing effect of apigenin and the five flavonoids were then investigated and their effects on the α, β, and γ globin genes expressions were compared using real-time PCR.
2.Effects of food formulation and thermal processing on flavones in celery and chamomile.
Hostetler GL;Riedl KM;Schwartz SJ Food Chem. 2013 Nov 15;141(2):1406-11. doi: 10.1016/j.foodchem.2013.04.051. Epub 2013 Apr 25.
Flavones isolated from celery varied in their stability and susceptibility to deglycosylation during thermal processing at pH 3, 5, or 7. Apigenin 7-O-apiosylglucoside was converted to apigenin 7-O-glucoside when heated at pH 3 and 100°C. Apigenin 7-O-glucoside showed little conversion or degradation at any pH after 5h at 100°C. Apigenin, luteolin, and chrysoeriol were most stable at pH 3 but progressively degraded at pH 5 or 7. Chamomile and celery were used to test the effects of glycosidase-rich foods and thermal processing on the stability of flavone glycosides. Apigenin 7-O-glucoside in chamomile extract was readily converted to apigenin aglycone after combination with almond, flax seed, or chickpea flour. Apigenin 7-O-apiosylglucoside in celery leaves was resistant to conversion by β-glucosidase-rich ingredients, but was converted to apigenin 7-O-glucoside at pH 2.7 when processed at 100°C for 90min and could then be further deglycosylated when mixed with almond or flax seed.
3.Liquid-liquid extraction for the enrichment of edible oils with phenols from olive leaf extracts.
Japón-Luján R;Luque de Castro MD J Agric Food Chem. 2008 Apr 9;56(7):2505-11. doi: 10.1021/jf0728810. Epub 2008 Mar 7.
A liquid-liquid extraction method to enrich edible oils--olive, sunflower, and soy oils--with phenols from olive leaf extracts is proposed. After microwave assistance to remove the phenols from three varieties of olive leaves, concentrations in the extracts between 12921 and 5173 mg/L of oleuropein, between 488 and 192 mg/L of apigenin-7-glucoside, between 444 and 219 mg/L of luteolin-7-glucoside, and between 501 and 213 mg/L of verbascoside were obtained, which clearly depended on the target variety. After optimization of the liquid-liquid extraction step, the concentrations in oils were 442, 162, and 164 mg/L of oleuropein, respectively, which were also enriched in apigenin-7-glucoside (between 8 and 15 mg/L, depending of the oil), lutelin-7-glucoside (between 11 and 12 mg/L), and verbascoside (between 11 and 13 mg/L). The oil-extract distribution factor of these compounds was also calculated for all olive leaf varieties and edible oils using different extracts concentrations and also different oil-extract volume ratios.
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CAS 578-74-5 Cosmosiin

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