[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Nishino et al., 1977 - Google Patents

Studies on the Synthesis of Proteinase Inhibitors I. Synthesis and Activity of Nonapeptide Fragments of Soybean Bowman-Birk Inhibitor

Nishino et al., 1977

View PDF
Document ID
13252481545164614366
Author
Nishino N
AOYAGI H
KATO T
IZUMIYA N
Publication year
Publication venue
The Journal of Biochemistry

External Links

Snippet

Ac, Y= NH2; Ib: X= H, Y= OH), which correspond to residues 14-22 in the sequence of Bowman-Birk inhibitor, have been synthesized by Merrifield's solid-phase method. Inhibitory activities of la and Ib on tryptic hydrolysis of amide and ester substrates were examined …
Continue reading at www.jstage.jst.go.jp (PDF) (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10Tetrapeptides
    • C07K5/1002Tetrapeptides with the first amino acid being neutral
    • C07K5/1005Tetrapeptides with the first amino acid being neutral and aliphatic
    • C07K5/1008Tetrapeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atoms, i.e. Gly, Ala
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0819Tripeptides with the first amino acid being acidic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0802Tripeptides with the first amino acid being neutral
    • C07K5/0804Tripeptides with the first amino acid being neutral and aliphatic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06008Dipeptides with the first amino acid being neutral
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/575Hormones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/06General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents
    • C07K1/061General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents using protecting groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/81Protease inhibitors
    • C07K14/8107Endopeptidase (E.C. 3.4.21-99) inhibitors
    • C07K14/811Serine protease (E.C. 3.4.21) inhibitors
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/107General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides
    • C07K1/1072General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides by covalent attachment of residues or functional groups
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICRO-ORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING OR MAINTAINING MICRO-ORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14Hydrolases (3)
    • C12N9/48Hydrolases (3) acting on peptide bonds (3.4)
    • C12N9/50Proteinases Endopeptidases (3.4.21-3.4.25)
    • C12N9/64Proteinases Endopeptidases (3.4.21-3.4.25) derived from animal tissue
    • C12N9/6421Proteinases Endopeptidases (3.4.21-3.4.25) derived from animal tissue from mammals
    • C12N9/6424Serine endopeptidases (3.4.21)
    • C12N9/6427Chymotrypsins (3.4.21.1; 3.4.21.2); Trypsin (3.4.21.4)
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K7/00Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04Linear peptides containing only normal peptide links

Similar Documents

Publication Publication Date Title
Carraway et al. The synthesis of neurotensin.
Püschel et al. Isolation and characterization of dipeptidyl peptidase IV from human placenta
Orlowski et al. A multicatalytical protease complex from pituitary that forms enkephalin and enkephalin containing peptides
US5607858A (en) Peptide amides, processes for the preparation thereof and agents containing these as fibrin/thrombin clotting inhibitors
Coggins et al. Affinity labelling of proteinases with tryptic specificity by peptides with C-terminal lysine chloromethyl ketone
EP0110306B1 (en) Chromogene compounds, process for their preparation and their use
CA1230069A (en) Modified protease inhibitors, process for their preparation, and pharmaceutical compositions prepared therefrom
Nakagawa et al. Synthesis of protected peptide segments and their assembly on a polymer-bound oxime: application to the synthesis of a peptide model for plasma apolipoprotein AI
Atherton et al. Peptide synthesis. Part 7. Solid-phase synthesis of conotoxin G1
Nishino et al. Studies on the Synthesis of Proteinase Inhibitors I. Synthesis and Activity of Nonapeptide Fragments of Soybean Bowman-Birk Inhibitor
Kageyama et al. Isolation of an activation intermediate and determination of the amino acid sequence of the activation segment of human pepsinogen A
Inouye et al. The Amino Acid Sequence of T4 Phage Lysozyme: IV. DILUTE ACID HYDROLYSIS AND THE ORDER OF TRYPTIC PEPTIDES
Han et al. Primary Structure of Bovine Plasma High-Molecular-Weight Kininogen The Amino Acid Sequence of a Glycopeptide Portion (Fragment 1) Following the C-Terminus of the Bradykinin Moiety
Ferjancic et al. Unusual specificity of polyethylene glycol-modified thermolysin in peptide synthesis catalyzed in organic solvents
Poerio et al. Assignment of the five disulfide bridges in an α‐amylase inhibitor from wheat kernel by fast‐atom‐bombardment mass spectrometry and Edman degradation
BASAK et al. Design and synthesis of novel inhibitors of prohormone convertases
Pomroy et al. Solubilization of hydrophobic peptides by reversible cysteine PEGylation
Liem et al. Mechanism of action of thrombin on fibrinogen: III. Partial mapping of the active sites of thrombin and trypsin
Nakaie et al. Inhibition of renin by conformationally restricted analogues of angiotensinogen
Terada et al. STUDIES ON THE SYNTHESIS OF PROTEINASE INHIBITORS: II. Synthesis of Cyclic Nonapeptide Fragments and Analogs Related to the Reactive Sites of Soybean Bowman‐Birk Inhibitor
HERNANDEZ et al. Chemical synthesis and characterization of the epidermal growth factor‐like module of human complement protease Clr
Ten Kortenaar et al. Semisynthesis of horse heart cytochrome c analogues from two or three fragments.
Breddam Carboxypeptidase S-1 from Penicillium janthinellum: enzymatic properties in hydrolysis and aminolysis reactions
Kortt et al. Specificity and pH dependence of ficin-catalyzed hydrolyses. Comparisons with bromelain specificity
US5059679A (en) Method of selectively sulfating peptides