Name | tectoridin |
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Synonyms |
4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-5-hydroxy-3-(4-hydroxyphenyl)-6-methoxy-
Tectorigenin 7-glucoside 4',5-Dihydro-6-methoxy-7-(o-glucoside)isoflavone 5-Hydroxy-3-(4-hydroxyphenyl)-6-methoxy-4-oxo-4H-chromen-7-yl β-D-glucopyranoside Shekanin tectoridin Tectoridin (7CI,8CI) 5-hydroxy-3-(4-hydroxyphenyl)-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one |
Description | Tectoridin is a isoflavone isolated from Maackia amurensis. Tectoridin is a phytoestrogen and activates estrogen and thyroid hormone receptors. Tectoridin exerts the estrogenic effects via ER-dependent genomic pathway and GPR30-dependent nongenomic pathway[1][2]. |
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Related Catalog | |
In Vitro | Tectoridin scarcely binds to ER alpha as compared to 17beta-estradiol and genistein[2]. Tectoridin induceds potent estrogenic effects, namely recovery of the population of cells in the S-phase after serum starvation, transactivation of the estrogen response element, and induction of MCF-7 cell proliferation[2]. Tectoridin induces estrogenic effect, and this effect is severely abrogated by treatment with U0126 ( MEK1/2 inhibitor). Tectoridin promotes phosphorylation of ERK1/2, but does not affect phosphorylation of ER alpha at Ser (118). It also increases cellular accumulation of cAMP[2]. |
References |
Density | 1.6±0.1 g/cm3 |
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Boiling Point | 798.1±60.0 °C at 760 mmHg |
Melting Point | 261.8-263.2ºC |
Molecular Formula | C22H22O11 |
Molecular Weight | 462.404 |
Flash Point | 279.7±26.4 °C |
Exact Mass | 462.116211 |
PSA | 179.28000 |
LogP | 0.29 |
Vapour Pressure | 0.0±3.0 mmHg at 25°C |
Index of Refraction | 1.695 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Hazard Codes | C |
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RIDADR | NONH for all modes of transport |
RTECS | DJ3090000 |
HS Code | 29389090 |
Precursor 0 | |
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DownStream 1 | |