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-3988308-A 优先权日:1974-11-04 标题 :(Tyr3, Tyr14)-SRIF and intermediates 发明人:SARANTAKIS DIMITRIOS 权利人:AMERICAN HOME PROD 摘要:The tetradecapeptide Ala-Gly-Tyr-Lys-Asn-Phe-Phe-Trp-Lys-Thr-Phe-Thr-Ser-Tyr-OH is described as well as novel intermediates used in the synthesis of such tetradecapeptide. This tetradecapeptide inhibits the release of growth hormone.
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.
专利号:US-4415493-A 优先权日:1982-05-11 标 题 :Immune modulator peptides 发明人:WEIGLE WILLIAM O; MORGAN EDWARD L 权利人:SCRIPPS CLINIC RES 摘要:A class of 23 or 24 amino acid peptides available by chemical synthesis or by enzymatic and chemical cleavage of IgG is described. The compounds are useful in modulating the immune response.
参考标题:Enantioselective Synthesis Of N-Protected α-Amino Acid Hydrazides 作者:Jean-Alain Fehrentz,Mathieu Bibian,Sarah El-Habnouni,Jean Martinez |发布日期:2009.4 摘要:A New, Mild, General, And Efficient Synthesis Of N-Protected î+/--Amino Acid Hydrazides Is Described. This Two-Step Preparation Uses N-Aminophthalimide As Protected Hydrazine To Prepare N-Protected î+/--Amino Acid Hydrazide Precursors, And Subsequent DePhthaloylation With An Aminomethyl Polystyrene Resin Yields N-Protected î+/--Amino Acid Hydrazides. It Has The Advantages Of Avoiding The Use Of The Toxic Hydrazine Reagent And Being Compatible With The Most Commonly Used N-Protecting Groups. This Strategy Is Particularly Interesting In The Case Of N-(9-Fluorenylmethoxycarbonyl)-Protected Amino Acids. Within The Limits Of Chiral Hplc Detection, No Epimerization Is Apparent.
合成参考文献
参考文献:10.1007/bf02442879|10.1023/a:1008826901053 摘要:Frochot C, Vanderesse R, Driou A, Linden G, Marraud M, Thong Cung M. A solid-phase synthesis of three aza-, iminoaza- and reduced aza-peptides from the same precursor. International Journal of Peptide Research and Therapeutics. 1997 Dec;4(4-6):219–25. doi: 10.1023/a:1008826901053.