Virtual screening applied in hit identification as LSD1 inhibitors, a epigenetic target for cancer treatment (2017)
- Authors:
- USP affiliated authors: EMERY, FLAVIO DA SILVA - FCFRP ; TROSSINI, GUSTAVO HENRIQUE GOULART - FCF
- Unidades: FCFRP; FCF
- Subjects: INIBIDORES DE ENZIMAS; ANTINEOPLÁSICOS
- Language: Inglês
- Imprenta:
- Publisher: International Union of Pure and Applied Chemistry (IUPAC)
- Publisher place: Durham
- Date published: 2017
- Source:
- Título do periódico: Proceedings
- Conference titles: World Chemistry Congress
-
ABNT
LIMA, Elys Juliane Cardoso et al. Virtual screening applied in hit identification as LSD1 inhibitors, a epigenetic target for cancer treatment. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 13 maio 2024. -
APA
Lima, E. J. C., Maltarollo, V. G., Ganesan, A., Emery, F. da S., & Trossini, G. H. G. (2017). Virtual screening applied in hit identification as LSD1 inhibitors, a epigenetic target for cancer treatment. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/ -
NLM
Lima EJC, Maltarollo VG, Ganesan A, Emery F da S, Trossini GHG. Virtual screening applied in hit identification as LSD1 inhibitors, a epigenetic target for cancer treatment [Internet]. Proceedings. 2017 ;[citado 2024 maio 13 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/ -
Vancouver
Lima EJC, Maltarollo VG, Ganesan A, Emery F da S, Trossini GHG. Virtual screening applied in hit identification as LSD1 inhibitors, a epigenetic target for cancer treatment [Internet]. Proceedings. 2017 ;[citado 2024 maio 13 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/ - QSAR studies on the human sirtuin 2 inhibition by non-covalent 7,5,2-anilinobenzamide derivatives
- Construction and validation of the 3D-structure of T. Cruzi sirtuin-2 by modeling threading
- Synthesis of two 'heteroaromatic rings of the future' for applications in medicinal chemistry
- Synthesis and docking study for compounds analogs of LSD1 inhibitor
- Insights into newly approved drugs from a medicinal chemistry perspective
- Hologram quantitative structure–activity relationship and comparative molecular interaction field analysis of aminothiazole and thiazolesulfonamide as reversible LSD1 inhibitors
- β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders
- Human sirtuin 2 inhibitors, their mechanisms and binding modes
- Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes
- Claisen rearrangement of hydroxynaphthoquinones: selectivity toward naphthofuran or α-xiloidone using copper salts and iodine
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