CAS: 5241-66-7; (R)-2-((Tert-Butoxycarbonyl)Amino)-4-(Methylthio)Butanoic Acid

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93000-03-4 112883-40-6 1152-62-1

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CAS号348-67-4 D-蛋氨酸 | CAS号24424-99-5 二碳酸二叔丁酯 | CAS号91177-57-0 (R)-(1-羟基-4-(甲硫... | CAS号119975-64-3 啡肽 | CAS号26060-98-0 B°C-D-蛋氨酸N-羟基琥珀酰亚胺酯 | CAS号69612-71-1 B°C-D-Met-Gly-OH | CAS号82611-48-1 B°C-Freidinger′...

📜D-蛋氨酸 反应生成 N-Boc-D-蛋氨酸
参考文献:某些含硫二肽和缬氨酰缬氨酸的银(i)配合物的形成常数
标题:某些含硫二肽和缬氨酰缬氨酸的银(i)配合物的形成常数
摘要:已经确定了在25oc和i = 0.10 Mol Dm-3(kno 3)时的形成常数,其中包括具有九个二肽的ag I配合物,这些二肽结合了含有一个(糖基蛋氨酸和蛋氨酸基甘氨酸)或两个硫供体原子的侧链. .在从相同的氨基酸和不同手性的形成在后一种情况下二肽进行了研究(例如,大号-Methionyl-大号-甲硫氨酸和大号-Methionyl-D蛋氨酸).将结果与缬氨酰缬氨酸进行比较.形成常数的值根据二肽的优选构象和ag的趋势来解释i与s-供体原子键合或通过形成二聚体配合物进行线性配位.
DOI:10.1039/dt9840002305

专利信息

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-7659364-B2
优先权日:2001-11-15
标 题 :N-methyl-homocysteines and their use as well as process for their production
发明人：WILLUHN MARC; PLATZEK JOHANNES; OTTOW ECKHARD; PETROV ORLIN; BORM CLAUDIA; HINZ DIRK; MANN GREGOR; LISTER-JAMES JOHN; WILSON DAVID M
权利人:CIS BIO INT
摘要:The synthesis of N-methyl-homocysteines and their use are described.

专利号:US-3941763-A
优先权日:1975-03-28
标题:PGlu-D-Met-Trp-Ser-Tyr-D-Ala-Leu-Arg-Pro-Gly-NH2 and intermediates
发明人：SARANTAKIS DIMITRIOS
权利人:AMERICAN HOME PROD
摘要:The synthesis of the decapeptide pGlu-D-Met-Trp-Ser-Tyr-D-Ala-Leu-Arg-Pro-Gly-NH2 by solid-phase techniques is described. The decapeptide inhibits LH release.