Top Suppliers:I want be here
  • BioBioPha
  • China
  • Product Name: tectoridin
  • Price: ¥Inquiry/20mg
  • Purity: 98.0%
  • Stocking Period: 1 Day
  • Contact: Xueping-Zheng



611-40-5

611-40-5 structure
611-40-5 structure
  • Name: tectoridin
  • Chemical Name: tectoridin
  • CAS Number: 611-40-5
  • Molecular Formula: C22H22O11
  • Molecular Weight: 462.404
  • Catalog: Biochemical Plant extracts
  • Create Date: 2018-08-25 21:59:21
  • Modify Date: 2024-01-02 10:19:50
  • 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].

Name tectoridin
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].
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

[1]. Shim M, et al. Tectoridin from Maackia amurensis modulates both estrogen and thyroid receptors.Phytomedicine. 2014 Apr 15;21(5):602-6.

[2]. Kang K, et al. Tectoridin, a poor ligand of estrogen receptor alpha, exerts its estrogenic effects via an ERK-dependent pathway.Mol Cells. 2009 Mar 31;27(3):351-7.

Density 1.6±0.1 g/cm3
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

RTECS NUMBER :
DJ3090000
CHEMICAL NAME :
4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-5-hydroxy-3-(4-hydroxyph enyl)-6-methoxy-
CAS REGISTRY NUMBER :
611-40-5
BEILSTEIN REFERENCE NO. :
0068384
LAST UPDATED :
199709
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C22-H22-O11
MOLECULAR WEIGHT :
462.44

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
4200 mg/kg
TOXIC EFFECTS :
Behavioral - altered sleep time (including change in righting reflex) Behavioral - somnolence (general depressed activity) Lungs, Thorax, or Respiration - dyspnea
REFERENCE :
NYKZAU Nippon Yakurigaku Zasshi. Japanese Journal of Pharmacology. (Nippon Yakuri Gakkai, c/o Kyoto Daigaku Igakubu Yakurigaku Kyoshitsu, Konoe-cho, Yoshida, Sakyo-ku, Kyoto 606, Japan) V.40- 1944- Volume(issue)/page/year: 64,186,1968
Hazard Codes C
RIDADR NONH for all modes of transport
RTECS DJ3090000
HS Code 29389090
Precursor  0

DownStream  1