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Pure Appl. Chem., 1984, Vol. 56, No. 5, pp. 595-624

http://dx.doi.org/10.1351/pac198456050595

IUPAC-IUB JOINT COMMISSION ON BIOCHEMICAL NOMENCLATURE

Nomenclature and symbolism for amino acids and peptides (Recommendations 1983)

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  • Dang Bobo, Kubota Tomoya, Mandal Kalyaneswar, Bezanilla Francisco, Kent Stephen B. H.: Native Chemical Ligation at Asx-Cys, Glx-Cys: Chemical Synthesis and High-Resolution X-ray Structure of ShK Toxin by Racemic Protein Crystallography. J. Am. Chem. Soc. 2013, 135, 11911. <http://dx.doi.org/10.1021/ja4046795>
  • Vela T, Selvarajan P, Freeda T H, Balasubramanian K: Growth and characterization of pure and semiorganic nonlinear optical Lithium Sulphate admixtured l-alanine crystal. Phys. Scr. 2013, 87, 045801. <http://dx.doi.org/10.1088/0031-8949/87/04/045801>
  • Alam Mohammad Jane, Ahmad Shabbir: Anharmonic vibrational studies of l-aspartic acid using HF and DFT calculations. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 2012, 96, 992. <http://dx.doi.org/10.1016/j.saa.2012.07.135>
  • Vishwanatha T. M., Narendra N., Chattopadhyay Basab, Mukherjee Monika, Sureshbabu Vommina V.: Synthesis of Selenoxo Peptides and Oligoselenoxo Peptides Employing LiAlHSeH. J Org Chern 2012, 77, 2689. <http://dx.doi.org/10.1021/jo2024703>
  • Segura-Campos Maira, Chel-Guerrero Luis, Betancur-Ancona David, Hernandez-Escalante Victor M.: Bioavailability of Bioactive Peptides. Food Rev Int 2011, 27, 213. <http://dx.doi.org/10.1080/87559129.2011.563395>
  • Amoureux Jean-Paul, Wang Qiang, Hu Bingwen, Lafon Olivier, Trébosc Julien, Deng Feng: Rapid analysis of isotopically unmodified amino acids by high-resolution 14N-edited 1H–13C correlation NMR spectroscopy. Chem Commun 2008, 6525. <http://dx.doi.org/10.1039/b816362f>
  • Krys'ko A. A., Kabanov V. M., Kabanova T. A., Belikova M. V., Mazepa A. V.: Synthesis and antiaggregative activity of derivatives of 3-aminopiperidine-2,6-diones and 3-aminopyrrolidine-2,5-diones. Pharm Chem J 1998, 32, 304. <http://dx.doi.org/10.1007/BF02580514>
  • NOMENCLATURE ANNOUNCEMENT. Archives of Biochemistry and Biophysics 1997, 344, 242. <http://dx.doi.org/10.1006/abbi.1997.0206>
  • Maletínskâ Lenka, Neugebauer Witold, Parê Marie-Christine, Pêrodin Jacqueline, Pham Dung, Escher Emanuel: Lipid Masking and Reactivation of Angiotensin Analogues. HCA 1996, 79, 2023. <http://dx.doi.org/10.1002/hlca.19960790723>
  • Seebach Dieter, Sommerfeld Thimo L., Jiang Qiongzhong, Venanzi Luigi M.: Preparation of Oxazolidine-Containing Peptides: Unusual effects in RhIII-catalyzed acetalizations of aldehydes with urethane-protected serine and threonine esters and with dipeptides containing serine or threonine residues at the N-terminus. HCA 1994, 77, 1313. <http://dx.doi.org/10.1002/hlca.19940770513>
  • Sommerfeld Thimo L., Seebach Dieter: Dehydroalanine-Containing Peptides by AcOH-Elimination fromO-Acetylserine Residuces with DBU/LiClO4 in Tetrahydrofuran. HCA 1993, 76, 1702. <http://dx.doi.org/10.1002/hlca.19930760427>
  • Kapurniotu Afroditi, Link Peter, Voelter W.: Total Synthesis of Thymosin β4 by Fragment Condensation. Liebigs Ann Chem 1993, 1993, 1161. <http://dx.doi.org/10.1002/jlac.1993199301188>
  • Spencker Torsten, Goppelt-Struebe Margarete, Keese Wolfgang, Resch Klaus, Rimpler Manfred: Klassische Synthese eines selektiven Peptid-Substrates für die Messung der Proteinkinase C. Liebigs Ann Chem 1993, 1993, 237. <http://dx.doi.org/10.1002/jlac.199319930142>
  • Armesto X. L., Canle L. M., Losada M., Santaballa J. A.: Nitrenium ions in N-chloro-α-amino acids decomposition?. Int J Chem Kinet 1993, 25, 1. <http://dx.doi.org/10.1002/kin.550250102>
  • Herranz Rosario, Suárez-Gea M.Luisa, García-López M.Teresa, González-Muñiz Rosario, Johansen Nils L., Madsen Kjeld, Thogersen Henning, Suzdak Peter: Solid phase synthesis of ψ[CH(CN)NH] pseudopeptides. Application to the synthesis of analogues of neurotensin [NT(8–13)]. Tetrahetron Lett 1993, 34, 8357. <http://dx.doi.org/10.1016/S0040-4039(00)61430-2>
  • Altmann Karl-Heinz, Altmann Eva, Mutter Manfred: Confromational Studies on Peptides Containing Enantiometric α-Methyl α-Amino Acids. Part I. Differential conformational properties of (R)- and (S)-2-methylaspartic acid. HCA 1992, 75, 1198. <http://dx.doi.org/10.1002/hlca.19920750420>
  • Kovács Lajos, Hesse Manfred: Synthetic Analogues of Naturally Occurring Spider Toxins. HCA 1992, 75, 1909. <http://dx.doi.org/10.1002/hlca.19920750617>
  • Kapurniotu Afroditi, Voelter Wolfgang: Totalsynthese von Thymosin β4, 2. Klassische Synthese des Fragments [20–30] von Thymosin β4. Liebigs Ann Chem 1992, 1992, 361. <http://dx.doi.org/10.1002/jlac.199219920164>
  • Seebach Dieter, Bossler Hans, Gründler Hansjörg, Shoda Shin-Ichiro, Wenger Roland: C-Alkylation of Peptides through Polylithiated and LiCl-Solvated Derivatives Containing Sarcosine Li-Enolate Units. HCA 1991, 74, 197. <http://dx.doi.org/10.1002/hlca.19910740121>
  • Scebach Dieter, Thaler Adrian, Blaser Denis, Ko Soo Y.: Transesterifications with 1,8-Diazabicyclo[5.4.0]undec-7-ene/Lithium Bromide (DBU/LiBr) - Also Applicable to Cleavage of Peptides from Resins inMerrifleld Syntheses. HCA 1991, 74, 1102. <http://dx.doi.org/10.1002/hlca.19910740520>
  • Kapurniotu Afroditi, Voelter Wolfgang: Totalsynthese von Thymosin β4, 1. Klassische Synthese des Fragments [11–19] von Thymosin β4. Liebigs Ann Chem 1991, 1991, 1251. <http://dx.doi.org/10.1002/jlac.1991199101216>
  • Wipf Peter, Heimgartner Heinz: Synthesis of Peptides Containing α,α-Disubstituted α-Amino Acids by the Azirine/Oxazolone Method: The (12-20)-Nonapeptide of the Ionophore Alamethicin. HCA 1990, 73, 13. <http://dx.doi.org/10.1002/hlca.19900730103>
  • Kalbacher Hubert, Jahan Meeno, Mihelić Mirna, Zaman Fakhar, Voelter Wolfgang: Solution synthesis of a biologically active fragment (33–41) of thymosin β9. Liebigs Ann Chem 1990, 1990, 249. <http://dx.doi.org/10.1002/jlac.199019900145>
  • Vliegenthart Hans: Nomenclature notes. Trends Biochem Sci Pers Ed 1989, 14, 496. <http://dx.doi.org/10.1016/0968-0004(89)90183-7>
  • Wipf Peter, Heimgartner Heinz: Anwendung der Azirin/Oxazolon-Methode in der Peptid-Chemie: Synthese von Modell-Tripeptiden. HCA 1988, 71, 140. <http://dx.doi.org/10.1002/hlca.19880710118>
  • Wipf Peter, Heimgartner Heinz: Konformationsanalysen von Modell-Tripeptiden: Der Einfluss von α,α-disubstituierten α-Aminosäuren auf die Sekundärstruktur. Teil I. NMR- und CD-Untersuchungen. HCA 1988, 71, 258. <http://dx.doi.org/10.1002/hlca.19880710129>
  • Wipf Peter, Kunz Roland W., Prewo Roland, Heimgartner Heinz: Konformationsanalysen von Modell-Tripeptiden: Der Einfluss von α,α-disubstituierten α-Aminosäuren auf die Sekundärstruktur. Teil II. Röntgenstrukturanalyse und Konformationsenergie-Berechnungen. HCA 1988, 71, 268. <http://dx.doi.org/10.1002/hlca.19880710130>
  • Shute Richard E., Kawai Megumi, Rich Daniel H.: Conformationally constrained biologically active peptides: tentative identification of the antimitogenic bioactive confomer of the naturally occurring cyclic tetrapeptides. Tetrahedron 1988, 44, 685. <http://dx.doi.org/10.1016/S0040-4020(01)86109-3>
  • Mackiewicz Zbignew, Bélisle Serge, Bellabarba Diego, Gallo-Payet Nicole, Lehoux Jean-Guy, Lagacé Ginette, Escher Emanuel: Synthesis and Placental Binding Potencies of Photosensitive Analogues of Luteinizing Hormone Releasing Hormone (LHRH) with Agonistic and Antagonistic Structures. HCA 1987, 70, 423. <http://dx.doi.org/10.1002/hlca.19870700221>
  • Kessler Horst, Steuernagel Stefan, Gillessen Dieter, Kamiyama Tsutomu: Complete Sequence Determination and Localisation of One Imino and Three Sulfide Bridges of the NonadecapeptideRo 09-0198 by Homonuclear 2D-NMR Spectroscopy. The DQF-RELAYED-NOESY-Experiment. HCA 1987, 70, 726. <http://dx.doi.org/10.1002/hlca.19870700322>
  • Minchev Stoyan, Sofroniev Nedyalko V.: The Use ofS-Acetamidomethyl-L-cysteine in the Synthesis of Glutathione, Glutathione Fragments, and Their Amides. Liebigs Ann Chem 1987, 1987, 69. <http://dx.doi.org/10.1002/jlac.198719870112>
  • Shute Richard E, Rich Daniel H: A novel double deprotection-peptide cyclisation procedure and its application to the synthesis of analogues of the cyclic tetrapeptide HC-toxin. Tetrahetron Lett 1987, 28, 3419. <http://dx.doi.org/10.1016/S0040-4039(00)96315-9>
  • Vorherr Thomas, Altmann Karl-Heinz, Mutter Manfred: Single-Centre Model for the Active Site of α-Chymotrypsin. HCA 1986, 69, 410. <http://dx.doi.org/10.1002/hlca.19860690221>
  • Wipf Peter, Heimgartner Heinz: Kupplung von Peptiden mit C-terminalen α,α-disubstituierten α - Aminosäurenvia Oxazol-5(4H)-one. HCA 1986, 69, 1153. <http://dx.doi.org/10.1002/hlca.19860690524>
  • Schwyzer Robert: Membrane structure and biologic activity of adrenocorticotropin (ACTH) and melanotropin (MSH) peptides. Estimation of structural parameters including the influence of the helix dipole moment. HCA 1986, 69, 1685. <http://dx.doi.org/10.1002/hlca.19860690724>
  • Schwyzer Robert, Erne Daniel, Rolka Krzysztof: Membrane Structure of Substance P. I. Prediction of Preferred Conformation, Orientation, and Accumulation of Substance P on Lipid Membranes. HCA 1986, 69, 1789. <http://dx.doi.org/10.1002/hlca.19860690802>
  • Rolka Krzysztof, Erne Daniel, Schwyzer Robert: Membrane Structure of Substance P. II. Secondary Structure of Substance P, [9-Leucine]substance P, and Shorter Segments in 2,2,2-Trifluoroethanol, Methanol, and on Liposomes Studied by Circular Dichroism. HCA 1986, 69, 1798. <http://dx.doi.org/10.1002/hlca.19860690803>
  • Erne Daniel, Rolka Krzysztof, Schwyzer Robert: Membrane Structure of Substance P. III. Secondary Structure of Substance P in 2,2,2-Trifluoroethanol, Methanol, and on Flat Lipid Membranes Studied by Infrared Spectroscopy. HCA 1986, 69, 1807. <http://dx.doi.org/10.1002/hlca.19860690804>
  • Wunderlin Rudolf, Minakakis Panagiota, Tun-Kyi Aung, Sharma Shub Dev, Schwyzer Robert: Melanotropin Receptors I. Synthesis and Biological Activity ofNα-(5-Bromovaleryl)-Nα-deacetyl-α-melanotropin. HCA 1985, 68, 1. <http://dx.doi.org/10.1002/hlca.19850680102>
  • Bizzozero Spartaco A., Dutler Hans, Franzstack Ruth, Rovagnati Bruno A.: Enzyme-Catalyzed Peptide-Bond Formation: Elastase- and δ-Chymotrypsin-Assisted Synthesis of Oligopeptides. HCA 1985, 68, 981. <http://dx.doi.org/10.1002/hlca.19850680424>
  • Eberle Alex N., Zeller Albert: Tritiation of Peptides to High Specific Radioactivity. Part 1. Synthesis and Biological Properties of [13-(3H4)Norvaline]-α-MSH and of [2,23-Bis((3H2)tyrosine)]ACTH(1-24). HCA 1985, 68, 1880. <http://dx.doi.org/10.1002/hlca.19850680711>
  • Schwyzer Robert, Felder Eduard, Merli-Failli Paola: The CAMET and CASET links for the synthesis of protected oligopeptides and oligodeoxynucleotides on solid and soluble supports. HCA 1984, 67, 1316. <http://dx.doi.org/10.1002/hlca.19840670518>
  • Mutter Manfred, Bellof Dieter: A New Base-Labile Anchoring Group for Polymer-Supported Peptide Synthesis. HCA 1984, 67, 2009. <http://dx.doi.org/10.1002/hlca.19840670739>