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10 Kilogram |
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Estra-1,3,5(10)-triene-3,17-diol,2-methoxy-, (17b)-? price Estra-1,3,5(10)-triene-3,17-diol,2-methoxy-, (17b)-? CA 362-07-2 Estra-1,3,5(10)-triene-3,17-diol,2-methoxy-, (17b)-? supplier in China
superior quality
2-METHOXYESTRADIOL Chemical Properties |
mp | 188-190°C |
storage temp. | −20°C |
solubility | DMSO: 10 mg/mL |
form | crystalline |
color | light yellow |
CAS DataBase Reference | 362-07-2(CAS DataBase Reference) |
Safety Information |
Hazard Codes | T,Xi |
Risk Statements | 23/24/25-36/37/38-48-61-60-46-45 |
Safety Statements | 22-26-36/37/39-45-53-36 |
RIDADR | UN 3077 9/PG 3 |
WGK Germany | 3 |
RTECS | KG7537500 |
MSDS Information |
Provider | Language |
---|---|
SigmaAldrich | English |
2-METHOXYESTRADIOL Usage And Synthesis |
Chemical Properties | Off-White Solid |
Usage | A natural metabolite of 17?Estradiol which is devoid of estrogenic activity. Inhibits cell proliferation and angiogenesis. Binds to the colchicine binding site of tubulin, and has been suggested to function as a natural regulator of microtubule a |
Usage | A natural metabolite of 17β-Estradiol which is devoid of estrogenic activity. Inhibits cell proliferation and angiogenesis. Binds to the colchicine binding site of tubulin, and has been suggested to function as a natural regulator of microtubule assembly |
Usage | 2-Methoxyestradiol is a tubulin polymerization inhibitor and also decreases HIF-1 activity. |
Usage | 2-Methoxyestradiol depolymerizes microtubules and blocks HIF-1α nuclear accumulation and HIF-transcriptional activity. Phase 2. |
Usage | 2-Methoxy 17β-Estradiol is a natural metabolite of 17β-Estradiol which is devoid of estrogenic activity. Inhibits cell proliferation and angiogenesis. 2-Methoxy 17β-Estradiol binds to the colchicine binding site of tubulin, and has been suggested to function as a natural regulator of microtubule assembly and function. |
Biological Activity | Apoptotic, antiproliferative and antiangiogenic agent, in vitro and in vivo ; acts via an estrogen receptor-independent mechanism. Induces p53-induced apoptosis via two pathways: activation of p38 and NF- κ B; and activation of JNK and AP-1 leading to Bcl-2 phosphorylation. Also upregulates death receptor 5 and binds to tubulin, inhibiting its assembly. |
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