2-Methoxyestradiol, an endogenous mammalian metabolite, inhibits tubulin polymerization by interacting at the colchicine site.
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Metabolic inactivation of estrogens in breast tissue by UDP-glucuronosyltransferase enzymes: an overview.Steroid ligands bind human sex hormone-binding globulin in specific orientations and produce distinct changes in protein conformationCrystal structure of human sex hormone-binding globulin in complex with 2-methoxyestradiol reveals the molecular basis for high affinity interactions with C-2 derivatives of estradiolThe novel Akt inhibitor Palomid 529 (P529) enhances the effect of radiotherapy in prostate cancer2-Methoxyestradiol, a promising anticancer agentCatechol-o-methyltransferase expression and 2-methoxyestradiol affect microtubule dynamics and modify steroid receptor signaling in leiomyoma cells.Double-stranded RNA-dependent protein kinase is involved in 2-methoxyestradiol-mediated cell death of osteosarcoma cells.Expression and cyclic variations of catechol-O-methyl transferase in human endometrial stroma.Reduced tumor growth in vivo and increased c-Abl activity in PC3 prostate cancer cells overexpressing the Shb adapter protein.Cytochrome 450 1B1 (CYP1B1) polymorphisms associated with response to docetaxel in Castration-Resistant Prostate Cancer (CRPC) patients.2-methoxyestradiol inhibits Barrett's esophageal adenocarcinoma growth and differentiation through differential regulation of the beta-catenin-E-cadherin axisEffects of estrogen metabolite 2-methoxyestradiol on tumor suppressor protein p53 and proliferation of breast cancer cells.Application of the McMurry coupling reaction in the synthesis of tri- and tetra-arylethylene analogues as potential cancer chemotherapeutic agentsA neurosteroid analogue photolabeling reagent labels the colchicine-binding site on tubulin: a mass spectrometric analysis.Cardiovascular protective effects of 17beta-estradiol metabolites.Judah Folkman, a pioneer in the study of angiogenesisInteractions of antimitotic peptides and depsipeptides with tubulin.Sulphamoylated 2-methoxyestradiol analogues induce apoptosis in adenocarcinoma cell lines.Superoxide dismutase: an emerging target for cancer therapeutics.Pregnenolone binds to microtubule-associated protein 2 and stimulates microtubule assembly.Drugs that target dynamic microtubules: a new molecular perspectiveEzrin, radixin, and moesin are phosphorylated in response to 2-methoxyestradiol and modulate endothelial hyperpermeability.Synergistic apoptosis of MCF-7 breast cancer cells by 2-methoxyestradiol and bis(ethyl)norsperminePregnancy ameliorates the inhibitory effects of 2-methoxyestradiol on angiogenesis in primary sheep uterine endothelial cellsHigh-throughput screening in niche-based assay identifies compounds to target preleukemic stem cells.A bis-sulphamoylated estradiol derivative induces ROS-dependent cell cycle abnormalities and subsequent apoptosis.2-Methoxyestradiol inhibits experimental autoimmune encephalomyelitis through suppression of immune cell activationA second-generation 2-Methoxyestradiol prodrug is effective against Barrett's adenocarcinoma in a mouse xenograft model.2-methoxyestradiol inhibits hypoxia-inducible factor-1{alpha} and suppresses growth of lesions in a mouse model of endometriosis.Development of new cancer therapeutic agents targeting mitosis.Pharmacokinetics and efficacy of 2-methoxyoestradiol and 2-methoxyoestradiol-bis-sulphamate in vivo in rodents.Anticancer drugs from nature--natural products as a unique source of new microtubule-stabilizing agents.Design, Synthesis and Antitumor Activity of Novel link-bridge and B-Ring Modified Combretastatin A-4 (CA-4) Analogues as Potent Antitubulin Agents.Direct modulation of microtubule stability contributes to anthracene general anesthesia.Syntheses and biological activities of novel 2-methoxyestradiol analogs, 2-fluoroethoxyestradiol and 2-fluoropropanoxyestradiol, and a radiosynthesis of 2-[(18)F]fluoroethoxyestradiol for positron emission tomography.BCRP expression does not result in resistance to STX140 in vivo, despite the increased expression of BCRP in A2780 cells in vitro after long-term STX140 exposure.Brain sex differences and hormone influences: a moving experience?Critical role of cyclin B1/Cdc2 up-regulation in the induction of mitotic prometaphase arrest in human breast cancer cells treated with 2-methoxyestradiol.Human pancreas-specific protein disulfide isomerase homolog (PDIp) is an intracellular estrogen-binding protein that modulates estrogen levels and actions in target cellsA novel monoclonal antibody to secreted frizzled-related protein 2 inhibits tumor growth.
P2860
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P2860
2-Methoxyestradiol, an endogenous mammalian metabolite, inhibits tubulin polymerization by interacting at the colchicine site.
description
1994 nî lūn-bûn
@nan
1994 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
2-Methoxyestradiol, an endogen ...... acting at the colchicine site.
@ast
2-Methoxyestradiol, an endogen ...... acting at the colchicine site.
@en
type
label
2-Methoxyestradiol, an endogen ...... acting at the colchicine site.
@ast
2-Methoxyestradiol, an endogen ...... acting at the colchicine site.
@en
prefLabel
2-Methoxyestradiol, an endogen ...... acting at the colchicine site.
@ast
2-Methoxyestradiol, an endogen ...... acting at the colchicine site.
@en
P2093
P2860
P356
P1476
2-Methoxyestradiol, an endogen ...... acting at the colchicine site.
@en
P2093
P2860
P304
P356
10.1073/PNAS.91.9.3964
P407
P577
1994-04-01T00:00:00Z