CAS: 90555-66-1; 3-Ethoxyphenylboronic Acid

该化合物是一种有机有机体化合物,通常在铃木-宫浦交叉相交反应中用作多功能中间体,其碳酸功能组可高效地与丙烯或丙酰卤化物交融,促进双亚烯和苯乙烯衍生物的合成.含乙氧代谢物的代谢性能可提高有机溶剂的溶性,并可在下游应用中影响电子特性.这种试剂在制药和材料科学研究中特别有用,因为需要控制芳香系统功能化.由于对丙烯或丙烯酸的敏感性,这种试剂通常在惰性条件下处理.该化合物的稳定性和再活动性特征使得它成为构建复杂的分子结构的一个实用选择.

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CAS号688-74-4 硼酸三丁酯 | CAS号202208-73-9 3-乙氧基-联苯-4-羧酸 | CAS号25117-75-3 3-乙氧基苯甲腈 | CAS号215433-92-4 6-(3-乙氧基-苯基)-1,... | CAS号43035-14-9 3-乙氧基二苯胺 | CAS号613660-99-4 [5-(3-ethoxyphe... | CAS号54852-73-2 1,1-Biphenyl, 3...

合成工艺路线路线简述

    硼酸三丁酯,Alkaline Earth Salt Of/the/ Methylsulfuric Acid置于乙醚体系中,化学反应生成 3-乙氧基苯硼酸
    参考文献:The Dissociation Constants Of The Chlorophenyl And Phenetyl Boric Acids1
    标题:The Dissociation Constants Of The Chlorophenyl And Phenetyl Boric Acids1
    摘要:
    DOI:10.1021/ja01319A053

    海关参考信息

    专利信息


    专利号:US-12187735-B2
    优先权日:2018-09-17
    标 题:Matter of composition, synthesis, formulation and application of FL118 platform positions 7 and 9-derived analogues for treatment of human disease
    发明人:LING XIANG; LI QINGYONG; LI FENGZHI
    权利人:CANGET BIOTEKPHARMA LLC
    摘要:Described herein, are the chemical synthesis, matter of compositions, formulation, function, methods and uses of the FL118 platform Positions 7 and/or 9-derived analogues for treating cancer or other human diseases. Compounds derived from chemical modifications of the FL118 platform are employed alone or in combination with other anti-cancer agents to preclude, eliminate or reverse cancer phenotypes. This invention intends to realize unique personalized cancer treatment (personalized precision medicine) through application of a series of structural relevant individual FL118 platform-derived analogues, which target multiple cellular human disease-relevant proteins and their signaling pathways.

    专利号:US-2025092058-A1
    优先权日:2018-09-17
    标 题 :Matter of composition, synthesis, formulation and application of fl 118 platform positions 7 and 9-derived analogues for treatment of human disease
    发明人:LING XIANG; LI QINGYONG; LI FENGZHI
    权利人:CANGET BIOTEKPHARMA LLC
    摘要:Described herein, are the chemical synthesis, compounds, methods and uses of the fluoroaryl-substituted derivatives at the FL118 position 7, which target multiple cellular human disease-relevant proteins and their signaling pathways.

    专利号:WO-9948868-A9
    优先权日:1998-03-26
    标 题 :Heterocyclic classes of compounds for the modulating tyrosine protein kinase
    发明人:FONG ANNIE; HANNAH ALISON; HARRIS G DAVIS; HIRTH PETER; HUBBARD STEVEN R; LANGECKER PETER; LIANG CONGXIN; MCMAHON GERALD; MOHAMMADI MOOSA; SCHLESSINGER JOSEPH; SHAWVER LAURA K; SUN LI; TANG PENG C; ULLRICH AXEL
    权利人:SUGEN INC; UNIV NEW YORK; MAX PLANCK INST FUR BIOCHEMIE; FONG ANNIE; HANNAH ALISON; HARRIS G DAVIS; HIRTH PETER; HUBBARD STEVEN R; LANGECKER PETER; LIANG CONGXIN; MCMAHON GERALD; MOHAMMADI MOOSA; SCHLESSINGER JOSEPH; SHAWVER LAURA K; SUN LI; TANG PENG C; ULLRICH AXEL
    摘要:The invention relates to certain indolinone-based and pyrazolylamide-based compounds, their method of synthesis, and combinatorial libraries consisting of the compounds. The invention also relates to methods of modulating the function of protein kinases using these compounds and methods of treating diseases by modulating the function of protein kinases and related signal transduction pathways.

    专利号:US-2004067531-A1
    优先权日:1997-08-20
    标 题:Methods of modulating protein tyrosine kinase function with substituted indolinone compounds
    发明人:TANG PENG CHO; SUN LI; TRAN NGOC MY; NGUYEN ANH THI; NEMATALLA ASAAD
    权利人:SUGEN INC
    摘要:The invention relates to certain indolinone compounds, their method of synthesis, and a combinatorial library consisting of the indolinone compounds. The invention also relates to methods of modulating the function of protein tyrosine kinases using indolinone compounds and methods of treating diseases by modulating the function of protein tyrosine kinases and related signal transduction pathways.

    专利号:US-6514981-B1
    优先权日:1998-04-02
    标题:Methods of modulating tyrosine protein kinase function with indolinone compounds
    发明人:TANG PENG CHO; SUN LI
    权利人:SUGEN INC
    摘要:The invention relates to certain indolinone compounds, their method of synthesis, and a combinatorial library consisting of the indolinone compounds. The invention also relates to methods of modulating the function of protein tyrosine kinases using indolinone compounds and methods of treating diseases by modulating the function of protein tyrosine kinases and related signal transduction pathways.

    专利号:US-7671085-B2
    优先权日:2002-11-15
    标 题 :Non-steroidal farnesoid X receptor modulators and methods for the use thereof
    发明人:DOWNES MICHAEL R; EVANS RONALD M
    权利人:SALK INST FOR BIOLOGICAL STUDI
    摘要:The efficient regulation of cholesterol synthesis, metabolism, acquisition, and transport is an essential component of lipid homeostasis. The farnesoid X receptor (FXR) is a transcriptional sensor for bile acids, the primary product of cholesterol metabolism. Accordingly, the development of potent, selective, small molecule agonists, partial agonists, and antagonists of FXR would be an important step in further deconvoluting FXR physiology. In accordance with the present invention, the identification of novel potent FXR activators is described. Two derivatives of invention compounds, bearing stilbene or biaryl moieties, contain members that are the most potent FXR agonists reported to date in cell-based assays. These compounds are useful as chemical tools to further define the physiological role of FXR as well as therapeutic leads for the treatment of diseases linked to cholesterol, bile acids and their metabolism and homeostasis.
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    合成参考文献


    参考文献:10.1021/acs.jmedchem.2c01165
    摘要:Barthel T, Wollenhaupt J, Lima GMA, Wahl MC, Weiss MS. Large-Scale Crystallographic Fragment Screening Expedites Compound Optimization and Identifies Putative Protein-Protein Interaction Sites. J Med Chem. 2022 Nov 10;65(21):14630–41. doi: 10.1021/acs.jmedchem.2c01165.
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