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

Mihara et al., 1984 - Google Patents

Cyclic peptides. XVI. Syntheses of AM‐toxin I analogs containing a lower or higher homolog of the component L‐2‐amino‐5‐(p‐methoxyphenyl) pentanoic acid …

Mihara et al., 1984

Document ID
16518039122037707410
Author
Mihara H
Aoyagi H
Lee S
Waki M
Kato T
Izumiya N
Publication year
Publication venue
International Journal of Peptide and Protein Research

External Links

Snippet

In order to investigate the influence of the side‐chain length at position 3 of AM‐toxin I (cyclic tetradepsipeptide) on necrotic activity for apple leaf, two analogs of AM‐toxin I,[L‐2‐amino‐4‐ (p‐methoxyphenyl) butanoic acid3]‐AM‐toxin I and [L‐2‐amino‐6‐(p‐methoxyphenyl) …
Continue reading at onlinelibrary.wiley.com (other versions)

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06—Dipeptides
    • C07K5/06008—Dipeptides with the first amino acid being neutral
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06—Dipeptides
    • C07K5/06086—Dipeptides with the first amino acid being basic
    • C07K5/06095—Arg-amino acid
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06—Esters of carbamic acids
    • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08—Tripeptides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/06—General 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
    • C07K1/061—General 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS

Similar Documents

Publication Publication Date Title
US5545662A (en) Urethanes and ureas that induce cytokine production
EP0123950A2 (en) Intermediates for thymosin alpha 1 and desacetylthymosin alpha 1
JPH01151600A (en) Cyclosporin
Lehmann et al. Synthesis of the Endothiopeptide BOC-Trp-Ile-Ala-Aib-Ile-Valψ [CSNH] Aib-Leu-Aib-Pro-OMe by a Variation of the ‘Azirine/Oxazolone Method’
US3821188A (en) Proline and pyroglutamic acid containing tripeptides
Wu et al. An Efficient Method for The Preparation of w, w′-bis-Urethane Protected Arginine Derivatives
Kogami et al. Synthesis of opically active 3-morpholinecarboxylic acid and tetrahydro-2H-1, 4-thiazine-3-carboxylic acid.
Mihara et al. Cyclic peptides. XVI. Syntheses of AM‐toxin I analogs containing a lower or higher homolog of the component L‐2‐amino‐5‐(p‐methoxyphenyl) pentanoic acid residue
US5138061A (en) Thioacylating reagents
Nichifor et al. Synthesis of peptide derivatives of 5-fluorouracil
Bland The first synthesis of a member of the iturin family, the antifungal cyclic lipopeptide, iturin-A2
EDWARDS et al. New synthesis and biological activity of the cyclic tetrapeptides tentoxin and [Pro 1] tentoxin
US4250086A (en) Method and composition for preparation of H-SAR-LYS-SAR-GLN-NH2
PT94159A (en) METHOD FOR PREPARING HETEROCYCLIC COMPOSITIONS CONTAINING AMINO AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
Sato et al. Studies of peptide antibiotics. XXXV. Synthesis of gramicidin S by a fragment solid-phase method.
US4369137A (en) N-Protected pentapeptides useful as intermediates in the preparation of thymopoietin pentapeptide
AOYAGI et al. Cyclic peptides. XVIII. Syntheses of AM‐toxin I analogs containing bulky L‐amino acid residues instead of an L‐alanine
JPH0578394A (en) Cell proliferation suppressant labeled with fucose
Kaur et al. Synthesis and Biological Evaluation of Dehydrophenylalanine Containing Substance P Fragments.
Mihara et al. Cyclic Peptides. XXII. Synthesis of [2-Amino-2, 3-dehydrobutanoic Acid4] AM-Toxin I
MIHARA et al. Cyclic peptides: XXI. Syntheses of AM‐toxin I analogs containing L‐lactic acid or L‐2‐hydroxy‐4‐methylpentanoic acid residue
US5457180A (en) Methods for producing linear thiopeptides using an amino acid ortho amino thioanilide compound
IL42973A (en) Polypeptides with acth activity containing an alpha-aminooxy carboxylic acid group on the n-terminal moiety
US3803117A (en) Tetrapeptide
Kanmera et al. Syntheses of AM-toxin III and its analogs using the Hofmann degradation