Hologram quantitative structure–activity relationship and comparative molecular interaction field analysis of aminothiazole and thiazolesulfonamide as reversible LSD1 inhibitors (2015)
- Authors:
- USP affiliated authors: HONORIO, KÁTHIA MARIA - EACH ; EMERY, FLAVIO DA SILVA - FCFRP ; TROSSINI, GUSTAVO HENRIQUE GOULART - FCF
- Unidades: EACH; FCFRP; FCF
- DOI: 10.4155/fmc.15.68
- Subjects: INIBIDORES DE ENZIMAS; ANTINEOPLÁSICOS; HOLOGRAMAS; RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Future Medicinal Chemistry
- ISSN: 1756-8919
- Volume/Número/Paginação/Ano: v. 7, n. 11, p. 1381-1394, 2015
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
MALTAROLLO, Vinícius Gonçalves et al. Hologram quantitative structure–activity relationship and comparative molecular interaction field analysis of aminothiazole and thiazolesulfonamide as reversible LSD1 inhibitors. Future Medicinal Chemistry, v. 7, n. 11, p. 1381-1394, 2015Tradução . . Disponível em: https://doi.org/10.4155/fmc.15.68. Acesso em: 13 fev. 2026. -
APA
Maltarollo, V. G., Honório, K. M., Emery, F. da S., Ganesa, A., & Trossini, G. H. G. (2015). Hologram quantitative structure–activity relationship and comparative molecular interaction field analysis of aminothiazole and thiazolesulfonamide as reversible LSD1 inhibitors. Future Medicinal Chemistry, 7( 11), 1381-1394. doi:10.4155/fmc.15.68 -
NLM
Maltarollo VG, Honório KM, Emery F da S, Ganesa A, Trossini GHG. Hologram quantitative structure–activity relationship and comparative molecular interaction field analysis of aminothiazole and thiazolesulfonamide as reversible LSD1 inhibitors [Internet]. Future Medicinal Chemistry. 2015 ; 7( 11): 1381-1394.[citado 2026 fev. 13 ] Available from: https://doi.org/10.4155/fmc.15.68 -
Vancouver
Maltarollo VG, Honório KM, Emery F da S, Ganesa A, Trossini GHG. Hologram quantitative structure–activity relationship and comparative molecular interaction field analysis of aminothiazole and thiazolesulfonamide as reversible LSD1 inhibitors [Internet]. Future Medicinal Chemistry. 2015 ; 7( 11): 1381-1394.[citado 2026 fev. 13 ] Available from: https://doi.org/10.4155/fmc.15.68 - Synthesis of two 'heteroaromatic rings of the future' for applications in medicinal chemistry
- Synthesis and docking study for compounds analogs of LSD1 inhibitor
- Virtual screening applied in hit identification as LSD1 inhibitors, a epigenetic target for cancer treatment
- Construction and validation of the 3D-structure of T. Cruzi sirtuin-2 by modeling threading
- QSAR studies on the human sirtuin 2 inhibition by non-covalent 7,5,2-anilinobenzamide derivatives
- Use of machine learning approaches for novel drug discovery
- Benchmark studies of UV-vis spectra simulation for cinnamates with UV filter profile
- In silico studies on the interaction between bioactive ligands and ALK5, a biological target related to the cancer treatment
- Simulação do espectro de absorção UV do filtro solar p-metoxicinamato de etilexila empregando métodos teóricos (TD-DFT)
- Understanding PPAR-δ affinity and selectivity using hologram quantitative structure–activity modeling, molecular docking and GRID calculations
Informações sobre o DOI: 10.4155/fmc.15.68 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
