On the Concept of Linear Modified Retro-Peptide Structures
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[1] M. Bergmann,et al. A METHOD FOR THE STEPWISE DEGRADATION OF POLYPEPTIDES , 1936 .
[2] G. Goissis,et al. Synthesis of biologically active retroenantiomers of angiotensin peptides. , 1976, Journal of Medicinal Chemistry.
[3] Harold A. Scheraga,et al. Structure of Water and Hydrophobic Bonding in Proteins. I. A Model for the Thermodynamic Properties of Liquid Water , 1962 .
[4] H. Gerlach,et al. Cycloenantiomerie und Cyclodiastereomerie. 1. Mitteilung , 1964 .
[5] H. Scheraga,et al. THE STRUCTURE OF WATER AND HYDROPHOBIC BONDING IN PROTEINS. III. THE THERMODYNAMIC PROPERTIES OF HYDROPHOBIC BONDS IN PROTEINS1,2 , 1962 .
[6] H. Scheraga,et al. Structure of Water and Hydrophobic Bonding in Proteins. IV. The Thermodynamic Properties of Liquid Deuterium Oxide , 1964 .
[7] Harold A. Scheraga,et al. Structure of Water and Hydrophobic Bonding in Proteins. II. Model for the Thermodynamic Properties of Aqueous Solutions of Hydrocarbons , 1962 .
[8] M. Koida,et al. EVALUATION OF THE PHYSIOLOGICAL PROPERTIES OF D-HISTIDYL-D-PHENYLALANYL-D-ARGINYL-D-TRYPTOPHYL-GLYCINE IN FROG MELANOCYTE. , 1964, Biochimica et biophysica acta.
[9] M. M. Shemyakin,et al. Topochemical Approach in Studies of the Structure–Activity Relation: Enantio-enniatin B , 1967, Nature.
[10] V. Prelog,et al. Cycloenantiomerie und Cyclodiastereomerie 2. Mitteilung. Über cycloenantiomere cyclo‐Hexaalanyle und ein cycloenantiomeres cyclo‐Diglycyl‐tetraalanyl , 1964 .
[11] W. Lergier,et al. Synthesen von Bradykinin‐Analogen mit D‐Arninosäuren (all‐D‐Bradykfnin und all‐D‐retro‐Bradikinin , 1966 .
[12] J. Morley,et al. Structure–Function Relationships in the Active C-Terminal Tetrapeptide Sequence of Gastrin , 1965, Nature.
[13] V. Prelog,et al. Über zwei cycloisomere Triglycyl‐tri‐L‐alanyle , 1966 .
[14] M. M. Shemyakin,et al. Topochemical investigations of peptide systems. , 1969, Angewandte Chemie.
[15] W. Lergier,et al. Synthese des Bradykininanalogen mit umgekehrter Aminosäuresequenz , 1962 .
[16] H. Scheraga. INTERMOLECULAR POTENTIAL FOR WATER AND THE HYDRATION OF PROTEINS * , 1977 .
[17] C. Li,et al. The synthesis of D-tryptophanyl-D-arginyl-D-phenylalanyl-D-histidyl-D-glutamic acid and its effect on melanotropic activity. , 1967, Biochimica et biophysica acta.
[18] H. Scheraga,et al. Energy parameters in polypeptides. VII. Geometric parameters, partial atomic charges, nonbonded interactions, hydrogen bond interactions, and intrinsic torsional potentials for the naturally occurring amino acids , 1975 .
[19] H. Scheraga,et al. Structure of liquid water. Statistical thermodynamic theory , 1972 .
[20] M. Ondetti,et al. SYNTHETIC PEPTIDES RELATED TO BRADYKININ , 1963 .
[21] W. Kauzmann. Some factors in the interpretation of protein denaturation. , 1959, Advances in protein chemistry.
[22] J. Stewart,et al. All-D-Bradykinin and the Problem of Peptide Antimetabolites , 1965, Nature.
[23] G. Flouret,et al. THE SYNTHESIS OF D-OXYTOCIN, THE ENANTIOMER OF THE POSTERIOR PITUITARY HORMONE, OXYTOCIN. , 1965, Journal of the American Chemical Society.
[24] T. Wieland,et al. Über Antamanid, XVI. all-D-retro-Antamanid und D-Tyr6-all-D-retro-antamanid , 1972 .
[25] J. Rudinger,et al. Amino-acids and peptides. XXXIII. Nitrosyl chloride and butyl nitrite as reagents in peptide synthesis by the azide method; Suppression of amide formation , 1961 .
[26] R. Studer,et al. Synthese von All-D-Val5-Angiotensin II-Asp1-?-Amid , 1965 .
[27] N. Grant,et al. Synthesis and biological activities of analogs of the luteinizing hormone-releasing hormone (LH-RH) modified in position 2. , 1974, Journal of medicinal chemistry.
[28] K. Bláha,et al. Amino acids and peptides. XCIV. Optical rotatory properties of diastereomeric cyclohexapeptides containing glycine, leucine, and phenylalanine , 1969 .
[29] K. Ninomiya,et al. Diphenylphosphoryl azide. A new convenient reagent for a modified Curtus reaction and for the peptide synthesis. , 1972, Journal of the American Chemical Society.