Rodríguez-Hernández et al., 2003 - Google Patents
Highly branched poly (L-lysine)Rodríguez-Hernández et al., 2003
- Document ID
- 11576840717808698589
- Author
- Rodríguez-Hernández J
- Gatti M
- Klok H
- Publication year
- Publication venue
- Biomacromolecules
External Links
Snippet
This paper describes the synthesis of several novel water-soluble highly branched polypeptides. The synthesis starts with the ring-opening polymerization of ε- benzyloxycarbonyl-l-lysine N-carboxyanhydride (Z-Lys NCA) or ε-trifluoroacetyl-l-lysine N …
- 229920000729 poly(L-lysine) polymer 0 title abstract description 44
Classifications
-
- 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
- A61K47/48169—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 modifying agent being an organic macromolecular compound, i.e. an oligomeric, polymeric, dendrimeric molecule
- A61K47/48192—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 modifying agent being an organic macromolecular compound, i.e. an oligomeric, polymeric, dendrimeric molecule the organic macromolecular compound has been obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas, polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/028—Polyamidoamines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
-
- 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
- A61K47/30—Macromolecular compounds
- A61K47/34—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, copolymers of polyalkylene glycol or poloxamer
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G83/00—Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
- C08G83/002—Dendritic macromolecules
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Rodríguez-Hernández et al. | Highly branched poly (L-lysine) | |
| Zhang et al. | Dynamic covalent polymers for biomedical applications | |
| Sun et al. | Direct formation of giant vesicles from synthetic polypeptides | |
| Hu et al. | Polysarcosine as an alternative to PEG for therapeutic protein conjugation | |
| Yuan et al. | Phenyl trimethylsilyl sulfide-mediated controlled ring-opening polymerization of α-amino acid N-carboxyanhydrides | |
| Klok et al. | Dendritic− graft polypeptides | |
| Huang et al. | Hydrolytically stable bioactive synthetic glycopeptide homo-and copolymers by combination of NCA polymerization and click reaction | |
| Putnam et al. | Poly (4-hydroxy-L-proline ester): Low-temperature polycondensation and plasmid DNA complexation | |
| Lu et al. | N-trimethylsilyl amines for controlled ring-opening polymerization of amino acid N-carboxyanhydrides and facile end group functionalization of polypeptides | |
| Fetsch et al. | Polypeptoids from N-substituted glycine N-carboxyanhydrides: Hydrophilic, hydrophobic, and amphiphilic polymers with poisson distribution | |
| Zhang et al. | Ugi reaction of natural amino acids: a general route toward facile synthesis of polypeptoids for bioapplications | |
| Zou et al. | A facile glovebox-free strategy to significantly accelerate the syntheses of well-defined polypeptides by N-carboxyanhydride (NCA) ring-opening polymerizations | |
| Gangloff et al. | Peptoids and polypeptoids at the frontier of supra-and macromolecular engineering | |
| Deng et al. | Synthesis and characterization of biodegradable poly (ester amide) s with pendant amine functional groups and in vitro cellular response | |
| Kricheldorf | Polypeptides and 100 years of chemistry of α‐amino acid N‐carboxyanhydrides | |
| Huesmann et al. | Revisiting secondary structures in NCA polymerization: influences on the analysis of protected polylysines | |
| EP1503802B1 (en) | Controllably degradable polymeric biomolecule or drug carrier and method of synthesizing said carrier | |
| Scales et al. | Corona-stabilized interpolyelectrolyte complexes of SiRNA with nonimmunogenic, hydrophilic/cationic block copolymers prepared by aqueous RAFT polymerization | |
| Huang et al. | Supramolecular hydrogels with reverse thermal gelation properties from (oligo) tyrosine containing block copolymers | |
| Harada et al. | Stabilized α-helix structure of poly (L-lysine)-block-poly (ethylene glycol) in aqueous medium through supramolecular assembly | |
| Zhang et al. | Water-soluble polypeptides with elongated, charged side chains adopt ultrastable helical conformations | |
| Xuan et al. | Synthesis and characterization of well-defined PEGylated polypeptoids as protein-resistant polymers | |
| Tao et al. | Synthesis and properties of alternating polypeptoids and polyampholytes as protein-resistant polymers | |
| Fagerland et al. | Short one-pot chemo-enzymatic synthesis of L-lysine and L-alanine diblock co-oligopeptides | |
| Krishna et al. | Synthesis of poly (propyl ether imine) dendrimers and evaluation of their cytotoxic properties |