Physico-chemical aspects of drug-membrane interactions (1991)
- Autor:
- Autor USP: SCHREIER, SHIRLEY - IQ
- Unidade: IQ
- Subjects: MEMBRANAS CELULARES; BIOQUÍMICA; INTERAÇÃO DE DROGAS
- Language: Inglês
- Imprenta:
- Publisher: Instituto de Quimica - Usp
- Publisher place: Sao Paulo
- Date published: 1991
- Source:
- Título do periódico: Resumos
- Conference titles: Workshop on Chemical Structure and Biological Activity
-
ABNT
SCHREIER, Shirley. Physico-chemical aspects of drug-membrane interactions. 1991, Anais.. Sao Paulo: Instituto de Quimica - Usp, 1991. . Acesso em: 23 abr. 2024. -
APA
Schreier, S. (1991). Physico-chemical aspects of drug-membrane interactions. In Resumos. Sao Paulo: Instituto de Quimica - Usp. -
NLM
Schreier S. Physico-chemical aspects of drug-membrane interactions. Resumos. 1991 ;[citado 2024 abr. 23 ] -
Vancouver
Schreier S. Physico-chemical aspects of drug-membrane interactions. Resumos. 1991 ;[citado 2024 abr. 23 ] - Nitroxide-solvent interaction: evaluation of the contribution of hydrogen bonding and van der waals interactions
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- Spin label study of local anesthetic-lipid membrane interactions. Phase separation of the uncharged form and bilayer micellization by the charged form of tetracaine cellization by the charged form of tetracaine
- Synthesis and interaction with membranes of a spin labeled pentadecapeptide contained in the sequence of an angiotensin ii receptor
- Pharmacological applications of spin labels .Involvement of membrane structural changes in the mechanism of drug action
- Esr studies of molecular aspects of the mechanism of drug action: antoxidation of the polyene antibiotic amphotericin b
- Metodo para determinacao do coeficiente de particao atraves da medida de alteracoes estruturais de membranas
- Effect of hemin on lipid membrane structure
- Chain-chain interactions within resins used for peptide synthesis: determination of distance and effective concentration through swelling and esr studies
- Synthetic and physico-chemical studies of benzhydrylamine resins with different substitution level: implications for solid phase peptide synthesis
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