Cosmosiin structure
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Common Name | Cosmosiin | ||
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CAS Number | 578-74-5 | Molecular Weight | 432.378 | |
Density | 1.6±0.1 g/cm3 | Boiling Point | 788.9±60.0 °C at 760 mmHg | |
Molecular Formula | C21H20O10 | Melting Point | 230-237ºC | |
MSDS | Chinese USA | Flash Point | 280.7±26.4 °C |
Use of CosmosiinApigenin-7-glucoside exhibits significant anti-proliferative and antioxidant activity, scavengers of ROS.In vitro: exhibits significant anti-proliferative activity against B16F10 melanoma cells after 24 and 48 h of incubation. Apigenin-7-glucoside provoks an increase of subG0/G1, S and G2/M phase cell proportion with a significant decrease of cell proportion in G0/G1 phases. Apigenin-7-glucoside enhances melanogenesis synthesis and tyrosinase activity of B16F10 melanoma cells. [1] Api7G specifically induced the differentiation of CD34+ cells towards the erythroid lineage and inhibited the myeloid differentiation. [2] APIG had strong antioxidant activity against reactive oxygen species (ROS) in vitro in a concentration-dependent manner. |
Name | apigenin 7-O-β-D-glucoside |
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Synonym | More Synonyms |
Description | Apigenin-7-glucoside exhibits significant anti-proliferative and antioxidant activity, scavengers of ROS.In vitro: exhibits significant anti-proliferative activity against B16F10 melanoma cells after 24 and 48 h of incubation. Apigenin-7-glucoside provoks an increase of subG0/G1, S and G2/M phase cell proportion with a significant decrease of cell proportion in G0/G1 phases. Apigenin-7-glucoside enhances melanogenesis synthesis and tyrosinase activity of B16F10 melanoma cells. [1] Api7G specifically induced the differentiation of CD34+ cells towards the erythroid lineage and inhibited the myeloid differentiation. [2] APIG had strong antioxidant activity against reactive oxygen species (ROS) in vitro in a concentration-dependent manner. |
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Related Catalog | |
References |
Density | 1.6±0.1 g/cm3 |
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Boiling Point | 788.9±60.0 °C at 760 mmHg |
Melting Point | 230-237ºC |
Molecular Formula | C21H20O10 |
Molecular Weight | 432.378 |
Flash Point | 280.7±26.4 °C |
Exact Mass | 432.105652 |
PSA | 170.05000 |
LogP | -0.39 |
Vapour Pressure | 0.0±2.9 mmHg at 25°C |
Index of Refraction | 1.717 |
Storage condition | 2-8°C |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
Precursor 0 | |
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DownStream 3 | |
Mesophyll distribution of 'antioxidant' flavonoid glycosides in Ligustrum vulgare leaves under contrasting sunlight irradiance.
Ann. Bot. 104(5) , 853-61, (2009) Flavonoids have the potential to serve as antioxidants in addition to their function of UV screening in photoprotective mechanisms. However, flavonoids have long been reported to accumulate mostly in ... |
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Antioxidant and antigenotoxic properties of compounds isolated from Marrubium deserti de Noé
Food Chem. Toxicol. 49(12) , 3328-35, (2011) Highlights ► We present here the purification of 13 compounds from an MeOH extract of Marrubium deserti. ► We measure antioxidant, genotoxic and antigenotoxic activites of six phenolic compounds. ► Tw... |
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Reliability of bond dissociation enthalpy calculated by the PM6 method and experimental TEAC values in antiradical QSAR of flavonoids.
Bioorg. Med. Chem. 18 , 28-35, (2010) The applicability of the newly developed RM1 and PM6 methods implemented in the semiempirical quantum chemistry mopac2009 software package in modeling free radical scavenging activity of flavonoids wa... |
Apigenin-7-O-Beta-D-glucopyranoside |
4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)- |
Apigenin 7-β-glucoside |
Cosmosiin |
MFCD00016787 |
Cosmosioside |
Apigenin 7-glucoside |
Apigenin-7-O-β-D-glucopyranoside |
Cosmosiin (8CI) |
Apigenin 7-β-D-glucoside |
Cosmiin |
Cosmosin |
Thalictiin |
apigenin 7-O-beta-D-glucoside |
Apigenin-7-O-glucoside |
Apigetrin |
COSMETIN |
Cosemetin |
EINECS 209-430-5 |
7-D-Glycosylapigenin |
5-Hydroxy-2-(4-hydroxyphényl)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxyméthyl)tétrahydro-2H-pyran-2-yl]oxy}-4H-chromén-4-one |
5-Hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl b-D-glucopyranoside |
Apigenin 7-O-β-D-glucopyranoside |
5-Hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl-β-D-glucopyranoside |
5-Hydroxy-2-(4-hydroxyphenyl)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}-4H-chromen-4-on |
7-(b-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one |
Cossmetin |
5-Hydroxy-2-(4-hydroxyphenyl)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}-4H-chromen-4-one |
Apigenin-7-d-glucoside |
Apigenin 7-O-β-glucoside |
Apigenin 7-β-D-glucopyranoside |
5-Hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl β-D-glucopyranoside |
Apigetrin,Cosmosiin |
Apigenin 7-O-glucoside |
4H-1-Benzopyran-4-one, 7- (β-D-glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)- |
Apigenin-7-glucoside |
Apigenin-7-O-β-glucopyranoside |
apigenin 7-O-β-D-glucoside |