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Amino Acids and Peptides. LIII. Synthesis and Biological Activities of Some Pseudo-Peptide Analogs of PKSI-527, a Plasma Kallikrein Selective Inhibitor. The Importance of the Peptide Backbone.

机译：氨基酸和肽。刘。 PKSI-527的一些伪肽类似物的合成和生物活性，血浆Kallikrein选择性抑制剂。肽骨干的重要性。

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Atsuko FUKUMIZU; Yoko TSUDA; Keiko WANAKA; Mayako TADA; Shosuke OKAMOTO; Akiko HIJIKATA-OKUNOMIYA; Yoshio OKADA;
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年度 1999
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1. Amino acids and peptides. LIII. Synthesis and biological activities of some pseudo-peptide analogs of PKSI-527, a plasma kallikrein selective inhibitor: the importance of the peptide backbone. [J] . Fukumizu A, Tsuda Y, Wanaka K, Chemical and Pharmaceutical Bulletin . 1999,第8期

机译：氨基酸和肽。 LIII。血浆激肽释放酶选择性抑制剂PKSI-527的某些伪肽类似物的合成和生物学活性：肽骨架的重要性。
2. Micelle-bound structures and dynamics of the hinge deleted analog of melittin and its diastereomer: implications in cell selective lysis by D-amino acid containing antimicrobial peptides. [J] . Saravanan R, Bhunia A, Bhattacharjya S Biochimica et biophysica acta. Biomembranes . 2010,第2期

机译：胶束结合的结构和蜂毒肽及其非对映异构体的铰链缺失类似物的动力学：在含D-氨基酸的抗菌肽对细胞的选择性裂解中的意义。
3. Synthesis, biological evaluation and molecular modeling of pseudo-peptides based statine as inhibitors for human tissue kallikrein 5 [J] . Hoelz Lucas V. B., Zorzanelli Bruna C., Azevedo Pedro Henrique R. de A., European Journal of Medicinal Chemistry: Chimie Therapeutique . 2016,第Null期

机译：基于伪肽的他汀类药物作为人体组织激肽释放酶5的抑制剂的合成，生物学评估和分子建模
4. Convenient conversion of amino acids to their N-hydroxylated derivatives on a solid support:synthesis of hydroxamate-based pseudo-peptides [C] . Yunpeng Ye, Garland R.Marshall the International Peptide Symposium . 2001

机译：在固体载体上方便地将氨基酸转化为其N-羟基化衍生物：基于羟胺的伪肽的合成
5. Part I. Application of 2-hydroxymethylacrylic acid, a product of Baylis-Hillman reaction, for the synthesis of novel N-backbone-to-side-chain cyclic peptide analogs: Strategies and side reactions. Part II. Synthesis and biological activities of chimeric bioactive peptides featuring amino acids coupled to 4-anilino-n-phenethyl-piperidine. [D] . Petrov, Ravil Rashitovich. 2007

机译：第一部分。Baylis-Hillman反应产物2-羟甲基丙烯酸在合成新型N骨架至侧链环状肽类似物中的应用：策略和副反应。第二部分具有与4-苯胺基-n-苯乙基-哌啶偶联的氨基酸的嵌合生物活性肽的合成和生物活性。
6. Synthesis of a novel category of pseudo-peptides using an Ugi three-component reaction of levulinic acid as bifunctional substrate amines and amino acid-based isocyanides [O] . Maryam Khalesi, Azim Ziyaei Halimehjani, Jürgen Martens 2019

机译：使用乙酰丙酸的乌吉三组分反应作为双功能底物胺和氨基酸基异氰酸酯合成新型伪肽
7. Studies on peptides. LIII. Synthesis of the docosapeptide corresponding to the entire amino acid sequence of porcine ACTH-like intermediate lobe peptide (CLIP). [O] . KANAME KOYAMA, YOSHIRO MORI, YOSHIAKI KISO, 1975

机译：肽研究。刘。对应于猪acth样中叶肽（夹子）的整个氨基酸序列的胚肽的合成。
8. Glutamate is the Endogenous Amino Acid Selectively Released by Rat Hippocampal Mossy Fiber Synaptosomes Concomitantly with Prodynorphin-Derived Peptides. [R] . Terrian, D. M., Gannon, R. L., Rea, M. A. 1990

机译：谷氨酸是由大鼠海马苔藓纤维突触体选择性释放的内源性氨基酸，同时与脯氨酸衍生肽一起释放。

Amino Acids and Peptides. LIII. Synthesis and Biological Activities of Some Pseudo-Peptide Analogs of PKSI-527, a Plasma Kallikrein Selective Inhibitor. The Importance of the Peptide Backbone.

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