Boronic acid and ester derivatives of L-cysteine: synthesis and their evaluation as proteasome inhibitors (2011)
- Authors:
- Autor USP: ANDRADE, LEANDRO HELGUEIRA DE - IQ
- Unidade: IQ
- Subjects: ANTINEOPLÁSICOS; ANTI-INFLAMATÓRIOS
- Language: Inglês
- Imprenta:
- Publisher: American Chemical Society
- Publisher place: Washington
- Date published: 2011
- Source:
- Título do periódico: Abstracts
- Conference titles: American Chemical Society National Meeting
-
ABNT
MILANI, Priscila e ANDRADE, Leandro Helgueira e DEMASI, Marilene. Boronic acid and ester derivatives of L-cysteine: synthesis and their evaluation as proteasome inhibitors. 2011, Anais.. Washington: American Chemical Society, 2011. . Acesso em: 23 abr. 2024. -
APA
Milani, P., Andrade, L. H., & Demasi, M. (2011). Boronic acid and ester derivatives of L-cysteine: synthesis and their evaluation as proteasome inhibitors. In Abstracts. Washington: American Chemical Society. -
NLM
Milani P, Andrade LH, Demasi M. Boronic acid and ester derivatives of L-cysteine: synthesis and their evaluation as proteasome inhibitors. Abstracts. 2011 ;[citado 2024 abr. 23 ] -
Vancouver
Milani P, Andrade LH, Demasi M. Boronic acid and ester derivatives of L-cysteine: synthesis and their evaluation as proteasome inhibitors. Abstracts. 2011 ;[citado 2024 abr. 23 ] - Magnetic bio-nanocomposite catalysts of 'CO''FE IND. 2''O IND. 4'/hydroxyapatite-lipase for enantioselective synthesis provide a framework for enzyme recovery and reuse
- Enzymatic reactions involving the heteroatoms from organic substrates
- Studies on terrein as a new class of proteasome inhibitors
- Síntese assimétrica de organoseleno aminas
- Hidrólise enantiosseletiva de 'beta'-boril-ésteres mediada por lipases
- Oxidation of organoselenium compounds: a study of chemoselectivity of phenylacetone monooxygenase
- Exploiting the enantioselectivity of Baeyer-Villiger monooxygenases via boron oxidation
- Synthesis of chiral organic selenium and tellurium compounds. The role of biocatalysis
- The 20s proteasome as target for antitumoral compounds: screenning for selective and reversible inhibitors among fungi-derived metabolites
- Resolução cinética de alcoóis primários através de reação de transesterificação catalisada por lipases
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