42
TITLE: A comparison of the structures of some 2- and 3-substituted chromone derivatives: a structural study on the importance of the secondary carboxamide backbone for the inhibitory activity of MAO-B
AUTHORS: Gomes, LR ; Low, JN; Cagide, F ; Alexandra Gaspar ; Borges, F ;
PUBLISHED: 2015, SOURCE: ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, VOLUME: 71, ISSUE: 11
INDEXED IN: Scopus WOS CrossRef: 2
43
TITLE: Crystal structures of two 6-(2-hydroxybenzoyl)-5H-thiazolo[3,2-a]pyrimidin-5-ones
AUTHORS: Gomes, LR ; Low, JN; Cagide, F ; Borges, F ;
PUBLISHED: 2015, SOURCE: ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, VOLUME: 71, ISSUE: 7
INDEXED IN: Scopus WOS CrossRef
44
TITLE: Discovery of two new classes of potent monoamine oxidase-B inhibitors by tricky chemistry
AUTHORS: Cagide, F ; Silva, T; Reis, J; Alexandra Gaspar ; Borges, F ; Gomes, LR ; Low, JN;
PUBLISHED: 2015, SOURCE: CHEMICAL COMMUNICATIONS, VOLUME: 51, ISSUE: 14
INDEXED IN: Scopus WOS CrossRef: 43
45
TITLE: New insights in the discovery of novel h-MAO-B inhibitors: structural characterization of a series of N-phenyl-4-oxo-4H-chromene-3-carboxamide derivatives
AUTHORS: Gomes, LR ; Low, JN; Cagide, F ; Chavarria, D ; Borges, F ;
PUBLISHED: 2015, SOURCE: ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, VOLUME: 71, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 4
46
TITLE: Porphyrin interaction with the membrane: The use of membrane models to elicit the diverse partition in normal and neoplastic tissue  Full Text
AUTHORS: Matos, C ; Ribeiro, C; Gomes, LR ;
PUBLISHED: 2015, SOURCE: Medicinal Chemistry Research, VOLUME: 24, ISSUE: 11
INDEXED IN: Scopus CrossRef
48
TITLE: The crystal structures of four N-(4-halophenyl)-4-oxo-4H-chromene-3-carboxamides
AUTHORS: Ligia R Gomes ; John Nicolson Low; Fernando Cagide ; Fernanda Borges ; Lough A.;
PUBLISHED: 2015, SOURCE: ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, VOLUME: 71, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
49
TITLE: Design, synthesis and biological evaluation of (E)-2-(2-arylhydrazinyl) quinoxalines, a promising and potent new class of anticancer agents  Full Text
AUTHORS: Felipe A R Rodrigues; Igor da S. Bomfim; Bruno C Cavalcanti; Claudia do O. Pessoa; James L Wardell; Solange M S V Wardell; Alessandra C Pinheiro; Carlos Roland Kaiser; Thais C M Nogueira; John N Low; Ligia R Gomes ; Marcus V N de Souza;
PUBLISHED: 2014, SOURCE: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, VOLUME: 24, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef
Page 5 of 11. Total results: 108.