Lee et al., 2020 - Google Patents
Stimulus-responsive conformational transformation of peptide with cell penetrating motif for triggered cytotoxicityLee et al., 2020
- Document ID
- 13877724770382437124
- Author
- Lee J
- Oh E
- Joo Y
- Kim H
- Park H
- Kim C
- Publication year
- Publication venue
- New Journal of Chemistry
External Links
Snippet
The KLA peptide, an antimicrobial peptide with an α-helical structure, needs to improve its low therapeutic efficacy and specificity for utilization as an anticancer agent. Here, we developed a modified KLA peptide (KLA-SS-R) with an intramolecular disulfide bond and a …
- 230000003013 cytotoxicity 0 title abstract description 22
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/08—Linear peptides containing only normal peptide links having 12 to 20 amino acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
-
- 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
- C07K5/10—Tetrapeptides
- C07K5/1002—Tetrapeptides with the first amino acid being neutral
- C07K5/1005—Tetrapeptides with the first amino acid being neutral and aliphatic
-
- 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
- C07K5/10—Tetrapeptides
- C07K5/1019—Tetrapeptides with the first amino acid being basic
-
- 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
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
-
- 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
- C07K14/001—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof by chemical synthesis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/06—Tripeptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives
- A61K47/48—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates
- A61K47/48007—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates the pharmacologically- or therapeutically-active agent being covalently bound or complexed to a modifying agent
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/10—Peptides having 12 to 20 amino acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/07—Tetrapeptides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/64—Cyclic peptides containing only normal peptide links
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Webber et al. | Switching of self-assembly in a peptide nanostructure with a specific enzyme | |
O'Connor et al. | The anti-cancer activity of a cationic anti-microbial peptide derived from monomers of polyhydroxyalkanoate | |
Zhu et al. | Substitution of the leucine zipper sequence in melittin with peptoid residues affects self-association, cell selectivity, and mode of action | |
Hadianamrei et al. | Rationally designed short cationic α-helical peptides with selective anticancer activity | |
Ahn et al. | Discovery of novel histidine-derived lipo-amino acids: applied in the synthesis of ultra-short antimicrobial peptidomimetics having potent antimicrobial activity, salt resistance and protease stability | |
JP6553706B2 (en) | Antimicrobial peptide dendrimer | |
CN104203262A (en) | Aromatic-cationic peptides and uses of same | |
Jones et al. | Mitoparan and target-selective chimeric analogues: membrane translocation and intracellular redistribution induces mitochondrial apoptosis | |
Zhou et al. | From a pro-apoptotic peptide to a lytic peptide: One single residue mutation | |
Baranyai et al. | In vitro biological evaluation of new antimycobacterial salicylanilide-tuftsin conjugates | |
Welsh et al. | Comparing dendritic and self-assembly strategies to multivalency—RGD peptide–integrin interactions | |
WO2018129171A1 (en) | Enzymatically activatable peptide-redox modulator conjugates and use thereof | |
Lee et al. | Stimulus-responsive conformational transformation of peptide with cell penetrating motif for triggered cytotoxicity | |
Czupiel et al. | Cationic block amphiphiles show anti-mitochondrial activity in multi-drug resistant breast cancer cells | |
Goel et al. | Fabrication of cationic nanostructures from short self-assembling amphiphilic mixed α/β-pentapeptide: Potential candidates for drug delivery, gene delivery, and antimicrobial applications | |
Li et al. | Total and semisyntheses of polymyxin analogues with 2-Thr or 10-Thr modifications to decipher the structure–activity relationship and improve the antibacterial activity | |
EP3102229B1 (en) | Anti-lymphoma peptides | |
Kim et al. | Cell-penetrating, amphipathic cyclic peptoids as molecular transporters for cargo delivery | |
Ahn et al. | Poly-lysine peptidomimetics having potent antimicrobial activity without hemolytic activity | |
RU2415868C1 (en) | Hemin derivatives, having antimicrobial activity or pharmaceutically acceptable salts thereof, synthesis method, pharmaceutical composition and use | |
Zhang et al. | Sepia ink oligopeptide induces apoptosis and growth inhibition in human lung cancer cells | |
Khalily et al. | Structure-based design, synthesis and anticancer effect of cyclic Smac–polyarginine peptides | |
Abou-Zied et al. | Elucidating the mechanism of peptide interaction with membranes using the intrinsic fluorescence of tryptophan: perpendicular penetration of cecropin B-like peptides into Pseudomonas aeruginosa | |
Kubi et al. | Cell-penetrating and mitochondrion-targeting molecules | |
Azmi et al. | Self-assembling lipopeptides with a potent activity against Gram-positive bacteria, including multidrug resistant strains |