Results 161 to 170 of about 7,932 (222)

Synthesis, cytotoxic screening and molecular docking, DFT calculation of novel furan-heterocyclic derivatives as insecticidal agents. [PDF]

Sci Rep
El-Kasabi HG, Girges MM, El-Salam SAA, Suliman AE, Abdel-Ghani GE.   +4 more
europepmc   +1 more source

Synthesis, antiproliferative activity targeting lung cancer and in silico studies of hydroxypiperidine substituted thiosemicarbazones. [PDF]

Sci Rep
Aftab H, Islam M, Şenol H, Batool Z, Ateşoğlu Ş, Çakır F, Akbaş F, Taslimi P, Alanazi AK, Noreen F, Shafiq Z.   +10 more
europepmc   +1 more source

Lysosome as a Chemical Reactor. [PDF]

Int J Mol Sci
Dharmasivam M, Kaya B.
europepmc   +1 more source

Reactivity of Acetylbarbituric Thiosemicarbazone Derivatives with Silver(I) Nitrate and the Influence of Substituents at Nitrogen Atom 4N on the Bonding and Nuclearity of the Resulting Silver(I) Complexes. [PDF]

ACS Omega
Castiñeiras A, Fernández-Hermida N, Frontera A, García-Santos I, Gómez-Rodríguez L.   +4 more
europepmc   +1 more source

Investigating Metal and Fluorophore Controlled Intracellular Localization in Noble Metal Thiosemicarbazone Complexes. [PDF]

Chemistry
Sheernaly N, Steinbrueck A, Krahn N, Rumancev C, Peeters F, Jusufagic L, Ochs J, Garrevoet J, Falkenberg G, Rosenhahn A, Metzler-Nolte N.   +10 more
europepmc   +1 more source

Antityrosinase and Antimicrobial Activities of trans-Cinnamaldehyde Thiosemicarbazone

Journal of Agricultural and Food Chemistry, 2009
Tyrosinase (EC 1.14.18.1) is a key enzyme in pigment biosynthesis of organisms. trans-Cinnamaldehyde thiosemicarbazone, a derivative of benzaldehyde thiosemicarbazone, was synthesized as an inhibitor of tyrosinase. The inhibitory effects of this compound
Yu-Jing Zhu, Kang-Kang Song, Qin Wang
exaly   +2 more sources

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Antifungal activity of thiosemicarbazones, bis(thiosemicarbazones), and their metal complexes

Journal of Inorganic Biochemistry, 2021
Fungi are ubiquitous in nature, and typically cause little or no environmental or pathogenic damage to their plant, animal, and human hosts. However, a small but growing number of pathogenic fungi are spreading world-wide at an alarming rate threatening global ecosystem health and proliferation.
Kritika, Bajaj, Robert M, Buchanan, Craig A, Grapperhaus   +2 more
openaire   +2 more sources

EPR characterization of a series of mono- and bis-thiosemicarbazone copper(II) complexes

Inorganica Chimica Acta, 1998
EPR studies at room and low temperatures of copper(II) complexes of acetaldehyde thiosemicarbazone (AlTSC), pyruvic acid thiosemicarbazone (PTSC) and ribose bis-thiosemicarbazone (RibTSC) have been undertaken.
Rebecca Pogni, Roberto Cao, Riccardo Basosi   +2 more
exaly   +2 more sources

Structure of salicylaldehyde thiosemicarbazone

Acta Crystallographica Section C Crystal Structure Communications, 1988
C8H9N3OS, monoclinic, C2/c, a = 14.206 (3), b = 14.244 (4), c = 10.457 (4) A, beta = 116.18(2) degrees, V = 1898.9 (8) A3, Z = 8, Dm = 1.387, D chi = 1.366 g cm-3, lambda(Mo K alpha) = 0.71069 A, mu = 2.90 cm-1, F(000) = 816.0, T = 298 K, final R = 0.0429 for 1322 observed reflections. The S and hydrazinic N atoms lie trans.
D, Chattopadhyay, S K, Mazumdar, T, Banerjee, S, Ghosh, T C, Mak   +4 more
openaire   +2 more sources

Biodistribution of 59Fe-thiosemicarbazones

International Journal of Nuclear Medicine and Biology, 1982
The 59Fe-iron(II) chelates of 2-formylpyridine thiosemicarbazone (I), 5-dimethylamino-2-formylpyridine thiosemicarbazone (II), and 5-hydroxy-2-formylpyridine thiosemicarbazone (III) were prepared and their biodistribution determined in normal rats. Early accumulation of these complexes occurred in the liver, muscle and pelt with lesser amounts in the ...
R N, Hanson, M A, Davis
openaire   +2 more sources