TY  - JOUR
AU  - Munoz, Javier
AU  - Cortes, Juan Carlos G
AU  - Sipiczki, Mátyás
AU  - Ramos, Mariona
AU  - Angel, Clemente-Ramos Jose
AU  - Belen, Moreno M
AU  - Martins, Ivone M
AU  - Perez, Pilar
AU  - Carlos, Ribas Juan
TI  - Extracellular cell wall beta(1,3) glucan is required to couple septation to actomyosin ring contraction
JF  - JOURNAL OF CELL BIOLOGY
J2  - J CELL BIOL
VL  - 203
PY  - 2013
IS  - 2
SP  - 265
EP  - 282
PG  - 18
SN  - 0021-9525
DO  - 10.1083/jcb.201304132
UR  - https://m2.mtmt.hu/api/publication/2802051
ID  - 2802051
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Keresztury, Gábor
AU  - Holly, Sándor
AU  - István, Krisztina
AU  - Sundius, T
AU  - Lóránd, Tamás
TI  - Analysis of vibrational spectra of some new E- and Z-4-arylidene-3-isochromanones Part 2. Isomers and conformers of the 2 '-pyrrolyl and 2 '-nitrophenyl derivatives
JF  - JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS
J2  - J BIOCHEM BIOPH METH
VL  - 61
PY  - 2004
IS  - 1-2
SP  - 107
EP  - 118
PG  - 12
SN  - 0165-022X
DO  - 10.1016/j.jbbm.2004.04.012
UR  - https://m2.mtmt.hu/api/publication/114815
ID  - 114815
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Lóránd, Tamás
AU  - Forgó, Péter
AU  - Foldesi, Andras
AU  - Osz, Erzsebet
AU  - Prókai, László
TI  - Improved solvent-free synthesis and structure elucidation of (E)- and (Z)-4-(arylmethylene)-3-isochromanones
JF  - EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
J2  - EUR J ORG CHEM
VL  - 2002
ET  - 0
PY  - 2002
IS  - 17
SP  - 2996
EP  - 3003
PG  - 8
SN  - 1434-193X
DO  - 10.1002/1099-0690(200209)2002:17<2996::AID-EJOC2996>3.0.CO;2-G
UR  - https://m2.mtmt.hu/api/publication/1329710
ID  - 1329710
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Al-Nakib, TM
AU  - Lóránd, Tamás
AU  - Foldesi, A
AU  - Varghese, R
TI  - The in vitro antimycotic activity and acute toxicity of third-generation bezylidenetetralones and heteroarylidenetetralones
JF  - MEDICAL PRINCIPLES AND PRACTICE
J2  - MED PRIN PRACT
VL  - 10
PY  - 2001
IS  - 4
SP  - 191
EP  - 196
PG  - 6
SN  - 1011-7571
DO  - 10.1159/000050368
UR  - https://m2.mtmt.hu/api/publication/1486611
ID  - 1486611
AB  - Objectives: A new series of E-2-arylmethylene-1-tetralones and E-2-heteroarylmethylene-1-tetralones (third generation) were designed as potential antimycotic agents against human pathogenic yeasts. Methods: The new compounds were obtained by aldol condensation of 1-tetralone with the appropriately substituted aldehydes in either acid- or base-catalysed conditions. These compounds were tested for their in vitro antimycotic activity against 24 strains of Cryptococcus neoformans, Candida spp. and Trichosporon cutaneum by a microtitre well technique in a liquid casitone medium, using a double dilution method. The toxicity of the new compounds was determined in vitro in cultured HeLa cells, in HeLa growth medium and in vivo in MFI mice. Results: Nineteen new E-2-benzylidine-1-tetralones were prepared, and 16 of the tested compounds showed superior antimycotic activity when compared to the first-generation E-2-benzylidine-1-tetralones synthesised previously. Twelve of these third-generation compounds were more active against different strains of yeasts than 6 commercial antimycotic agents similarly tested. An in vitro toxicity study and an in vivo acute toxicity study in MA mice showed that these compounds were severalfold less toxic than most of the commerical antimycotics, with 4 being comparable to or less toxic than the least toxic of the commercial agents (amphotericin B) tested by the same procedures. Conclusions: Twelve members of this new E-2-benzylidine-1-tetralone class of compounds are promising candidates for antimycotic agents worthy of further investigation. Copyright (C) 2001 S. Karger AG, Basel.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Williamson, RT
AU  - Marquez, BL
AU  - Gerwick, WH
AU  - E Kövér, Katalin
TI  - One- and two-dimensional gradient-selected HSQMBC NMR experiments for the efficient analysis of long-range heteronuclear coupling constants
JF  - MAGNETIC RESONANCE IN CHEMISTRY
J2  - MAGN RESON CHEM
VL  - 38
PY  - 2000
IS  - 4
SP  - 265
EP  - 273
PG  - 9
SN  - 0749-1581
DO  - 10.1002/(SICI)1097-458X(200004)38:4<265::AID-MRC637>3.0.CO;2-#
UR  - https://m2.mtmt.hu/api/publication/1154229
ID  - 1154229
AB  - Three new gradient-selected NMR experiments for the analysis of long-range heteronuclear coupling constants are presented. They are demonstrated on a series of compounds including sucrose, strychnine and a complex macrolide, phormidolide, isolated from a marine cyanobacterium. These 1D and 2D heteronuclear single quantum multiple bond correlation (HSQMBC) experiments provide pure absorption, antiphase lineshapes for precise, direct measurement of (n)J(C,H) coupling constants. The example compounds were chosen to demonstrate the high sensitivity and ease of spectral interpretation provided by these HSQMBC experiments. In addition, suppression of one-bond CH correlations has been introduced into the HSQMBC pulse sequence. Copyright (C) 2000 John Wiley & Sons, Ltd.
LA  - English
DB  - MTMT
ER  -