合成目标产物 L-Cysteine Ethyl Ester Hydrochloride 主要起始原料 Ethanol And L-Cysteine
52-90-4 = 868-59-7 反应条件:1.1 Reagents: Thionyl Chloride; Cooled; 12 H,Reflux 标题:Design,Synthesis And Cytotoxic Evaluation Of A Novel Series Of Benzo[d]Thiazole-2-Carboxamide Derivatives As Potential Egfr Inhibitors 作者:Zhang,Lan; Et Al 参考文献:Medicinal Chemistry Research 日期:2017 卷标:26(9) 页码:2180-2189]
52-90-4 = 868-59-7 反应条件:1.1 Reagents: Hydrochloric Acid Solvents: Ethanol 标题:Synthesis Of Compounds Of 5-Fluorouracil Containing Cysteine And Glutamic Acid 作者:Mukherji,G.; Et Al 参考文献:Pharmazie 日期:1989 卷标:44(8)
专利号:US-8653238-B2 优先权日:2006-02-27 标题:Compositions and methods for transport of molecules with enhanced release properties across biological barriers 发明人:WENDER PAUL A; GOUN ELENA A; JONES LISA R 权利人:WENDER PAUL A; GOUN ELENA A; JONES LISA R; UNIV LELAND STANFORD JUNIOR 摘要:Conjugates of a cargo molecule with a transporter molecule are disclosed, where the cargo molecule and the transporter molecule are linked covalently by a releasable linker. The cargo of the conjugate can be a biologically active agent or a reporter molecule. The transporter modulates the transport of the cargo across a biological barrier (e.g., a cell membrane) compared to the transport of the unconjugated cargo. Releasable linkers suitable for rapid and facile conjugation to various types of cargo and transporters are also disclosed, along with methods for using the linkers in the synthesis of conjugates.
专利号:EP-3030516-B1 优先权日:2013-08-07 标题:The synthesis of core-shell metal-semiconductor nanomaterials 发明人:REVAPRASADU NEERISH; DUNPALL REKHA 权利人:UNIV OF ZULULAND
专利号:US-2019031650-A1 优先权日:2016-01-29 标 题 :Dna alkylation and cross-linking agents as compounds and payloads for targeted therapies 发明人:HERZON SETH; HEALY ALAN; CRAWFORD JASON; VIZCAINO MARIA; NIKOLAYEVSKIY HERMAN 权利人:UNIV YALE 摘要:The present invention is directed to compounds related to precolibactin pharmaceutical compositions based upon these compounds and methods of synthesis which are employed to provide intermediates and final compounds, which are principally alkylating agents and anticancer compounds. The chemical synthetic approach disclosed facilitates the synthesis of numerous precolibactin analogs which can be used in the treatment of cancer.
专利号:US-6849650-B2 优先权日:1998-02-27 标 题:Heterocyclic compounds, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds 发明人:THORSETT EUGENE D; PORTER WARREN J; NISSEN JEFFREY S; LATIMER LEE H; AUDIA JAMES E; DROSTE JAMES 权利人:ATHENA NEUROSCIENCES INC; LILLY CO ELI 摘要:Disclosed are compounds which inhibit β-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions comprising a compound which inhibits β-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.
专利号:US-2012282652-A1 优先权日:2011-02-28 标题 :Preparation of peptide mixtures by protease catalysis designed to provide useful biological and physical properties 发明人:GROSS RICHARD A; VISWANATHAN KODANDARAMAN; QIN XU 权利人:GROSS RICHARD A; VISWANATHAN KODANDARAMAN; QIN XU; POLITECHNIC INST UNIV NEW YORK 摘要:A process for preparing unique peptide mixtures with a broad range of uses using combinations of natural and non-natural amino acid alkyl ester monomers and specific combinations of these monomers as dimers, trimers and higher oligomers selected from the large group of structural motifs that lead to useful physical and/or biological properties and that have been or may be identified from solid state peptide synthesis, isolation of peptides from natural sources, and production of peptides by recombinant DNA methods, or identification of peptides by recombinant methods such as phage display, the method of peptide synthesis comprising a) admixing one or more natural and non-natural amino acid alkyl ester monomer, dimer, trimer and higher oligomers with one or more proteases in a reaction medium; b) heating the mixture to between about 5° C. to about 90° C. for between 5 minutes and 24 hours; and c) recovering the formed oligopeptide.
专利号:WO-8707529-A1 优先权日:1986-06-16 标题:Segmented polymers and method for the synthesis thereof 发明人:BROOK BASIL WILLIAM; DUNK WILLIAM ALBERT EDWARD; BAGULEY MAURICE EDWARD; SAVILLE BRIAN 权利人:COURTAULDS PLC 摘要:A surface active agent contains at least one radical generator group in each of its lipophilic and hydrophilic moieties. A water-in-oil dispersion or oil-in-water dispersions contains a first polymerisable monomer dissolved in the oil phase and a second monomer dissolved in the oil phase and a second monomer dissolved in the aqueous phase. A surface active agent as defined above is dispersed across the interface of the oil phase and the aqueous phase with its lipophilic moiety well solvated by the oil phase and its hydrophilic moiety well solvated by the aqueous phase. A segmented polymer comprising such a surface active agent having at least one lipophilic polymer segment attached to its lipophilic moiety and at least one hydrophilic polymer segment attached to its hydrophilic moiety can be formed from the dispersion.
参考标题:Synthesis And Antibacterial Evaluation Of 1β-Methyl-2-(5-Substituted Heterocyclic Carbamoyl)Pyrrolidin-3-Ylthio)Carbapenem Derivatives 作者:Joo-Shin Lee,Jung-Hyuck Choa,Heeyeong Cho,Chang-Hyun Oh |发布日期:2004.7 摘要:>The Synthesis Of A New Series Of 1β‐methylcarbapenems Having A Substituted Heterocyclic Carbamoyl Pyrrolidine Moiety Is Described. Their In Vitro Antibacterial Activity Against Both Gram‐positive And Gram‐negative Bacteria Was Tested, And The Effect Of Heterocyclic Substituents On The Pyrrolidine Was Investigated. One Particular Compound (Iiid) Having A Substituted Oxadiazole Moiety Showed The Most
合成参考文献
摘要:Nicolai, S.; Waser, J., Science of Synthesis: Hypervalent Halogens in Organic Synthesis, (2025) .