CAS: 70642-86-3; Boc-D-Tyr-Oh

相似化合物

1164-16-5 3978-80-1 556-02-5

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CAS号556-02-5 D-酪氨酸 | CAS号24424-99-5 二碳酸二叔丁酯 | CAS号76757-90-9 丁氧羰基-D-酪氨酸-甲氧基酯 | CAS号687-51-4 亮氨酰胺 | CAS号3728-20-9 D-酪氨酸甲酯盐酸盐 | CAS号58632-95-4 2-(叔-丁氧基碳酰胺)-2-苯乙腈 | CAS号1070-19-5 Carbonazidic ac... | CAS号3417-91-2 L-酪氨酸甲酯盐酸盐 | CAS号76757-92-1 N-叔丁氧羰基-O-乙基-D-酪氨酸

Dl-酪氨酸置于吡啶,氯化亚砜,三乙胺体系中,化学反应生成 Boc-D-酪氨酸
参考文献:Turan; Bajusz,Acta Chimica Academiae Scientiarum Hungaricae,1981,Vol. 107,# 1,P. 7-9
标题:Turan; Bajusz,Acta Chimica Academiae Scientiarum Hungaricae,1981,Vol. 107,# 1,P. 7-9

专利信息

专利号:WO-2010077155-A1
优先权日:2008-12-31
标 题 :A method of producing an n-blocked peptide
发明人：LIPKOWSKI ANDRZEJ
权利人:ACTION FOR DEV OF RES SP Z O O; LIPKOWSKI ANDRZEJ
摘要:The perspective uses of using peptides as drags require economical synthesis methods. It was shown that N-blocked peptide derivatives constituting the raw material for use in peptide synthesis may be obtained through the modification of the synthesis, which is based on the acylation of an appropriate organic amino-acid salt using an appropriate active derivative of an amino-acid or peptide.

专利号:US-2014309424-A1
优先权日:2011-06-30
标题:Direct synthesis of 18f-fluoromethoxy compounds for pet imaging and the provision of new precursors for direct radiosynthesis of protected derivatives of o-([18f] fluoromethyl) tyrosine
发明人：BRUMBY THOMAS; GRAHAM KEITH; KRUGER MARTIN
权利人:BRUMBY THOMAS; GRAHAM KEITH; KRUGER MARTIN; PIRAMAL IMAGING SA
摘要:The invention describes novel direct synthesis methods for converting a precursor into a PET-tracer with a 18 F-fluoromethoxy-group. The invention is also directed to novel and stable precursors for the direct radiosynthesis of protected derivatives of O—([ 18 F]Fluoromethyl)tyrosines.

专利号:US-2004110228-A1
优先权日:2002-04-01
标 题:Combinatorial organic synthesis of unique biologically active compounds
发明人：MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M
摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.

专利号:US-5783577-A
优先权日:1995-09-15
标题 :Synthesis of quinazolinone libraries and derivatives thereof
发明人：HOUGHTEN RICHARD A; OSTRESH JOHN M
权利人:TREGA BIOSCIENCES INC
摘要:The present invention provides synthetic combinatorial libraries of organic compounds based on the quinazolinone ring.

专利号:WO-9710221-A1
优先权日:1995-09-15
标 题:Synthesis of quinazolinone libraries
发明人：HOUGHTEN RICHARD A; OSTRESH JOHN M
权利人:TORREY PINES INST
摘要:The present invention provides synthetic combinatorial libraries of organic compounds based on the quinazolinone ring.

专利号:US-6989401-B2
优先权日:2000-07-19
标题:Sulfonic acid derivatives of hydroxamic acids and their use as medicinal products
发明人：MAEDA KAZUHIRO; SONDA SHUJI; TAKEMOTO TADAHIRO; GOTO TOMOKAZU; KOBAYASHI FUJIO; KAJII MASAHIKO; KOMORITA NARUYASU; HIRAYAMA FUMIHIRO
权利人:MITSUBISHI PHARMA CORP
摘要:The present invention relates to a novel sulfonic acid derivative of hydroxamic acid or a pharmacologically acceptable salt thereof. More particularly, the present invention relates to a sulfonic acid derivative of hydroxamic acid or a pharmacologically acceptable salt thereof, which is useful as an inhibitor of lipopolysaccharides (LPS). In addition, the present invention relates to a novel intermediate compound useful for the synthesis of this sulfonic acid derivative of hydroxamic acid.