Pregled bibliografske jedinice broj: 587868
STRUCTURAL INVESTIGATIONS OF AROYLHYDRAZONES
STRUCTURAL INVESTIGATIONS OF AROYLHYDRAZONES // Book of abstract / Radu Oprean (ur.).
Cluj - Napoca, 2012. str. 56-56 (pozvano predavanje, nije recenziran, sažetak, znanstveni)
CROSBI ID: 587868 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
STRUCTURAL INVESTIGATIONS OF AROYLHYDRAZONES
Autori
Galić, Nives
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of abstract
/ Radu Oprean - Cluj - Napoca, 2012, 56-56
Skup
12th INTERNATIONAL SYMPOSIUM AND SUMMER SCHOOL ON BIOANALYSIS
Mjesto i datum
Cluj-Napoca, Rumunjska, 04.07.2012. - 14.07.2012
Vrsta sudjelovanja
Pozvano predavanje
Vrsta recenzije
Nije recenziran
Ključne riječi
aroylhydrazones; keto-enol tautomery; E-Z isomerisation
Sažetak
Aroylhydrazones have been intensively investigated in resent years due to their versatile properties and applications. Many compounds of this type are biologically active as anticancer, antibacterial and antimicrobial agents. Hydrazones derived from isonicotinoyl hydrazide have been investigated as potential drugs for treatment of iron-overload associated diseases. In addition, this class of iron chelators showed remarkable antimalarial activity. Recent studies have shown that nicotinic acid hydrazones could be considered as a novel pharmacophore in the design of anticonvulsant drugs. Aroylhydrazones can be involved in keto-enol tautomeric interconversion. Tautomeric equilibrium can involve hydrazide part of the molecule, but also and aldehyde moiety if the hydroxyl group is situated in ortho position with respect to the C=N double bond. Apart from tautomeric interconversion, E–Z isomerisation of hydrazones due to solvent effect, pH value or UV irradiation can also occur. Different tautomeric and isomeric forms have different spectral properties and can be distinguished according to their IR, UV-Vis and NMR spectra. Since E/Z isomers can have diverse chelating properties as well as pharmacodynamic activities, the study of such equilibrium is relevant not only from theoretical point of view, but for further development of aroylhydrazones as potential drug candidates. In this lecture the results of structural investigations of aroylhydrazones derived from nicotinic acid hydrazide and various aldehydes in solid state and in solution by different spectrometric techniques will be given. In addition, the tautomeric interconversion upon complexation of transition-metal cations will be discussed as well.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
119-1191342-1083 - Interakcije i dizajn bioaktivnih molekula (Novak, Predrag, MZOS ) ( CroRIS)
119-1191342-2960 - Elektroliti i koordinacijske reakcije u otopini (Tomišić, Vladislav, MZOS ) ( CroRIS)
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Nives Galić
(autor)