PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection

Permanent URI for this collectionhttps://hdl.handle.net/11147/7645

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Now showing 1 - 9 of 9
  • Article
    Citation - WoS: 22
    Citation - Scopus: 22
    Fluorescein Propiolate: a Propiolate- Decorated Fluorescent Probe With Remarkable Selectivity Towards Cysteine
    (Royal Society of Chemistry, 2019) Karakuş, Erman; Sayar, Melike; Dartar, Suay; Kaya, Beraat Umur; Emrullahoğlu, Mustafa
    A fluorescent probe decorated with an alkynyl ester unit (e.g. propiolate) displayed a selective turn-on type fluorescent response towards cysteine. Following a sequential addition-cyclisation pathway mediated by the addition of cysteine, the pre-fluorescent dye rapidly transformed into a new structure and induced a fluorescent response clearly observable with the naked eye.
  • Article
    Citation - WoS: 36
    Citation - Scopus: 37
    A Bodipy-Based Fluorescent Probe for Ratiometric Detection of Gold Ions: Utilization Of: Z -Enynol as the Reactive Unit
    (Royal Society of Chemistry, 2016) Üçüncü, Muhammed; Karakuş, Erman; Emrullahoğlu, Mustafa
    Using an irreversible intramolecular cyclisation pathway triggered by gold ions, a boron-dipyrromethene (BODIPY) based fluorescent probe integrated with a reactive Z-enynol motif responds selectively to gold ions. With the addition of gold(iii), the probe displays ratiometric fluorescence behaviour clearly observable to the naked eye under both visible and UV light. © The Royal Society of Chemistry 2016.
  • Article
    Citation - WoS: 33
    Citation - Scopus: 36
    Epr Studies of Intermolecular Interactions and Competitive Binding of Drugs in a Drug-Bsa Binding Model
    (Royal Society of Chemistry, 2016) Akdoğan, Yaşar; Emrullahoğlu, Mustafa; Tatlıdil, Diğdem; Üçüncü, Muhammed; Çakan Akdoğan, Gülçin
    Understanding intermolecular interactions between drugs and proteins is very important in drug delivery studies. Here, we studied different binding interactions between salicylic acid and bovine serum albumin (BSA) using electron paramagnetic resonance (EPR) spectroscopy. Salicylic acid was labeled with a stable radical (spin label) in order to monitor its mobilized (free) or immobilized (bound to BSA) states. In addition to spin labeled salicylic acid (SL-salicylic acid), its derivatives including SL-benzoic acid, SL-phenol, SL-benzene, SL-cyclohexane and SL-hexane were synthesized to reveal the effects of various drug binding interactions. EPR results of these SL-molecules showed that hydrophobic interaction is the main driving force. Whereas each of the two functional groups (-COOH and -OH) on the benzene ring has a minute but detectable effect on the drug-protein complex formation. In order to investigate the effect of electrostatic interaction on drug binding, cationic BSA (cBSA) was synthesized, altering the negative net charge of BSA to positive. The salicylic acid loading capacity of cBSA is significantly higher compared to that of BSA, indicating the importance of electrostatic interaction in drug binding. Moreover, the competitive binding properties of salicylic acid, ibuprofen and aspirin to BSA were studied. The combined EPR results of SL-salicylic acid/ibuprofen and SL-ibuprofen/salicylic acid showed that ibuprofen is able to replace up to ∼83% of bound SL-salicylic acid, and salicylic acid can replace only ∼14% of the bound SL-ibuprofen. This indicates that ∼97% of all salicylic acid and ibuprofen binding sites are shared. On the other hand, aspirin replaces only ∼23% of bound SL-salicylic acid, and salicylic acid replaces ∼50% of bound SL-aspirin, indicating that ∼73% of all salicylic acid and aspirin binding sites are shared. These results show that EPR spectroscopy in combination with the spin labeling technique is a very powerful method to investigate drug binding dynamics in detail.
  • Article
    Citation - WoS: 5
    Citation - Scopus: 5
    A Rare ?-Pyranopyrazole Skeleton: Design, One-Pot Synthesis and Computational Study
    (Royal Society of Chemistry, 2016) Üçüncü, Muhammed; Cantürk, Ceren; Karakuş, Erman; Zeybek, Hüseyin; Bozkaya, Uğur; Soydaş, Emine; Şahin, Ertan; Emrullahoğlu, Mustafa
    Drawing upon a consecutive amide coupling and intramolecular cyclisation pathway, a one-pot, straightforward synthetic route has been developed for a range of pyrazole fused γ-pyrone derivatives. The reaction mechanism proposed for the chemoselective formation of γ-pyranopyrazole is furthermore fully supported by experimental and computational studies. © The Royal Society of Chemistry 2016.
  • Article
    Citation - WoS: 118
    Citation - Scopus: 121
    A Rhodamine/Bodipy-Based Fluorescent Probe for the Differential Detection of Hg(II) and Au(III)
    (Royal Society of Chemistry, 2014) Karakuş, Erman; Üçüncü, Muhammed; Emrullahoğlu, Mustafa
    We described the design and synthesis of a molecular sensor based on a rhodamine/BODIPY platform that displayed differential fluorescence responses towards Hg2+ and Au3+ and demonstrated its utility in intracellular ion imaging.
  • Article
    Citation - WoS: 60
    Citation - Scopus: 62
    A Bodipy-Based Reactive Probe for the Detection of Au(iii) Species and Its Application To Cell Imaging
    (Royal Society of Chemistry, 2014) Üçüncü, Muhammed; Emrullahoğlu, Mustafa
    A BODIPY-based fluorescent probe bearing a pyridyl hydrazone motif responds selectively to Au(III) ions through an irreversible C[double bond, length as m-dash]N bond hydrolysis reaction. Gold species, besides their ability to catalyse chemical transformations in organic synthesis,1 have significant impacts on human health.2,3 Gold-based drugs have long been used in the treatment of rheumatoid arthritis and other autoimmune diseases.2 At the same time, when accumulated in the biological system at certain concentrations, gold species have the potential to disturb a series of cellular processes by irreversible interaction with biomolecules.3 In recent years, fluorescence-based sensing has become an indispensable tool for sensitive and accurate detection of trace levels of metal species in the solution.4 In addition, with the aid of fluorescence microscopy it has become possible to track metal species in living cells, which is of crucial importance for elucidating their roles in the biological system.
  • Article
    Citation - WoS: 44
    Citation - Scopus: 46
    A Rhodamine Based "turn-On" Chemodosimeter for Monitoring Gold Ions in Synthetic Samples and Living Cells
    (Royal Society of Chemistry, 2013) Emrullahoğlu, Mustafa; Karakuş, Erman; Üçüncü, Muhammed
    A rhodamine-based fluorescent probe, functionalized with an alkyne moiety, shows highly selective recognition towards Au(i) and Au(iii) ions over other metal ions. Probe 1 is successfully employed for the determination of residual gold species in synthetic samples and monitoring the accumulation of gold ions in living cells.
  • Article
    Citation - WoS: 163
    Citation - Scopus: 167
    A Bodipy Aldoxime-Based Chemodosimeter for Highly Selective and Rapid Detection of Hypochlorous Acid
    (Royal Society of Chemistry, 2013) Emrullahoğlu, Mustafa; Üçüncü, Muhammed; Karakuş, Erman
    A BODIPY-based fluorescent probe integrated with an aldoxime unit shows a remarkable fluorescence "turn-on" response to hypochlorous acid (HOCl). The oxidative dehydrogenation of BODIPY aldoxime by HOCl results in a distinct fluorescence enhancement as well as a change in color from red to orange.
  • Article
    Citation - WoS: 59
    Citation - Scopus: 59
    Gold(i)/Zn(ii) Catalyzed Tandem Hydroamination/Annulation Reaction of 4-Yne
    (Royal Society of Chemistry, 2010) Demir, Ayhan S.; Emrullahoğlu, Mustafa; Buran, Kerem
    The tandem hydroamination-annulation reaction of 4-pentyne-nitriles in the presence of amine nucleophiles and a cooperatively operating catalyst system, consisting of Ph3PAuCl and Zn(ClO4)2, provides an efficient route to 2-aminopyrroles. Two regioisomeric 2-aminopyrroles were formed in moderate to good yields. © 2010 The Royal Society of Chemistry.