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101.
Hasan H. Hasanov Ivaylo K. Ivanov 《Phosphorus, sulfur, and silicon and the related elements》2020,195(10):858-870
AbstractWe report herein a study on the competitive electrophilic cyclization of 5-(dimethoxyphosphoryl)-alka-3,4-dienoates involving 5-endo-trig and 6-endo-trig mode cyclizations. Reaction with electrophiles produces mixtures of the 2-(2-oxo-2,5-dihydro-1,2-oxaphosphol-5-yl)-alkanoates and (6-oxo-5,6-dihydro-2H-pyran-2-yl)-phosphonates by competitive electrophilic cyclization due to the participation of the neighboring phosphonate and carboxylate groups. 相似文献
102.
Hosseinikhah Seyed Mahdi Beigzadeh Borhan Siavashi Majid Halabian Mahdi 《Journal of Thermal Analysis and Calorimetry》2020,141(5):1543-1558
Journal of Thermal Analysis and Calorimetry - High interstitial fluid pressure in the tumor is among the most important barriers to drug delivery. The use of the static magnetic field is one of the... 相似文献
103.
Tahira Foyzun Abdullah Al Mahmud Md. Salim Ahammed Md. Imran Nur Manik Md. Kamrul Hasan KM Monirul Islam Simin Sobnom Lopa Md. Yusuf Al-Amin Kushal Biswas Mst. Rejina Afrin AHM Khurshid Alam Golam Sadik 《Molecules (Basel, Switzerland)》2022,27(3)
Neurotoxicity is a serious health problem of patients chronically exposed to arsenic. There is no specific treatment of this problem. Oxidative stress has been implicated in the pathological process of neurotoxicity. Polyphenolics have proven antioxidant activity, thereby offering protection against oxidative stress. In this study, we have isolated the polyphenolics from Acacia nilotica and investigated its effect against arsenic-induced neurotoxicity and oxidative stress in mice. Acacia nilotica polyphenolics prepared from column chromatography of the crude methanol extract using diaion resin contained a phenolic content of 452.185 ± 7.879 mg gallic acid equivalent/gm of sample and flavonoid content of 200.075 ± 0.755 mg catechin equivalent/gm of sample. The polyphenolics exhibited potent antioxidant activity with respect to free radical scavenging ability, total antioxidant activity and inhibition of lipid peroxidation. Administration of arsenic in mice showed a reduction of acetylcholinesterase activity in the brain which was counteracted by Acacia nilotica polyphenolics. Similarly, elevation of lipid peroxidation and depletion of glutathione in the brain of mice was effectively restored to normal level by Acacia nilotica polyphenolics. Gallic acid methyl ester, catechin and catechin-7-gallate were identified in the polyphenolics as the major active compounds. These results suggest that Acacia nilotica polyphenolics due to its strong antioxidant potential might be effective in the management of arsenic induced neurotoxicity. 相似文献
104.
Halilibrahim Ciftci Belgin Sever Firdevs Ocak Nilüfer Bayrak Mahmut Yldz Hatice Yldrm Hasan DeMirci Hiroshi Tateishi Masami Otsuka Mikako Fujita Ama Fatih TuYuN 《Molecules (Basel, Switzerland)》2022,27(3)
Plants have paved the way for the attainment of molecules with a wide-range of biological activities. However, plant products occasionally show low biological activities and/or poor pharmacokinetic properties. In that case, development of their derivatives as drugs from the plant world has been actively performed. As plant products, plastoquinones (PQs) have been of high importance in anticancer drug design and discovery; we have previously evaluated and reported the potential cytotoxic effects of a series of PQ analogs. Among these analogs, PQ2, PQ3 and PQ10 were selected for National Cancer Institute (NCI) for in vitro screening of anticancer activity against a wide range of cancer cell lines. The apparent superior anticancer potency of PQ2 on the HCT-116 colorectal cancer cell line than that of PQ3 and PQ10 compared to other tested cell lines has encouraged us to perform further mechanistic studies to enlighten the mode of anti-colorectal cancer action of PQ2. For this purpose, its apoptotic effects on the HCT-116 cell line, DNA binding capacity and several crucial pharmacokinetic properties were investigated. Initially, MTT assay was conducted for PQ2 at different concentrations against HCT-116 cells. Results indicated that PQ2 exhibited significant cytotoxicity in HCT-116 cells with an IC50 value of 4.97 ± 1.93 μM compared to cisplatin (IC50 = 26.65 ± 7.85 μM). Moreover, apoptotic effects of PQ2 on HCT-116 cells were investigated by the annexin V/ethidium homodimer III staining method and PQ2 significantly induced apoptosis in HCT-116 cells compared to cisplatin. Based on the potent DNA cleavage capacity of PQ2, molecular docking studies were conducted in the minor groove of the double helix of DNA and PQ2 presented a key hydrogen bonding through its methoxy moiety. Overall, both in vitro and in silico studies indicated that effective, orally bioavailable drug-like PQ2 attracted attention for colorectal cancer treatment. The most important point to emerge from this study is that appropriate derivatization of a plant product leads to unique biologically active compounds. 相似文献
105.
Aye Ünlü Kerem Teral Zübeyde Uurlu Aydn Ali A. Dnmez Hasan Soliman Yusufolu hsan al 《Molecules (Basel, Switzerland)》2022,27(3)
Polygala species are frequently used worldwide in the treatment of various diseases, such as inflammatory and autoimmune disorders as well as metabolic and neurodegenerative diseases, due to the large number of secondary metabolites they contain. The present study was performed on Polygala inexpectata, which is a narrow endemic species for the flora of Turkey, and resulted in the isolation of nine known compounds, 6,3′-disinapoyl-sucrose (1), 6-O-sinapoyl,3′-O-trimethoxy-cinnamoyl-sucrose (tenuifoliside C) (2), 3′-O-(O-methyl-feruloyl)-sucrose (3), 3′-O-(sinapoyl)-sucrose (4), 3′-O-trimethoxy-cinnamoyl-sucrose (glomeratose) (5), 3′-O-feruloyl-sucrose (sibiricose A5) (6), sinapyl alcohol 4-O-glucoside (syringin or eleutheroside B) (7), liriodendrin (8), and 7,4′-di-O-methylquercetin-3-O-β-rutinoside (ombuin 3-O-rutinoside or ombuoside) (9). The structures of the compounds were determined by the spectroscopic methods including 1D-NMR (1H NMR, 13C NMR, DEPT-135), 2D-NMR (COSY, NOESY, HSQC, HMBC), and HRMS. The isolated compounds were shown in an in silico setting to be accommodated well within the inhibitor-binding pockets of myeloperoxidase and inducible nitric oxide synthase and anchored mainly through hydrogen-bonding interactions and π-effects. It is therefore plausible to suggest that the previously established anti-inflammatory properties of some Polygala-derived phytochemicals may be due, in part, to the modulation of pro-inflammatory enzyme activities. 相似文献
106.
Nili-Ahmadabadi Mahdi Nematollahi Omid Fatehi Mostafa Cho Dae Seung Kim Kyung Chun 《显形杂志》2020,23(4):591-603
Journal of Visualization - Airfoils are mostly inefficient in their off-design conditions. In order to improve the aerodynamic performance of airfoils in these conditions, using an optimized cavity... 相似文献
107.
108.
A conformational study of the biomolecules released from submicron- and micron-sized temperature-sensitive composite polymer
particles by decreasing the temperature from 40 to 25 °C was done with circular dichroism and the results were compared with
those of the native biomolecules. In almost all cases the biomolecules released retained their native conformational states.
Received: 10 April 2001 Accepted: 13 June 2001 相似文献
109.
Hasan M. Khan Shagufta Naz Safia Tabassum 《Journal of Radioanalytical and Nuclear Chemistry》2011,289(1):225-229
Aqueous solution of crystal violet has been evaluated spectrophotometrically as a gamma-ray chemical dosimeter. The response
of the chemical dosimetric system has also been investigated under different environmental conditions, such as light and temperature.
In the present study the response has been measured at two wavelengths; 588 nm (λmax of the irradiated solution) and 500 nm. The response of the crystal violet dosimeter was linear in the dose range of 50–550 Gy
at pH 5.6 when absorption measurements were made at 588 and 500 nm. The response of the crystal violet dosimeter during post-irradiation
storage at room temperature in dark showed slight decrease in absorbance at 588 and 510 nm but the response was almost stable
at 460 nm. For higher doses, the change in the response was greater as compared to the low doses. Post-irradiation stability
during diffused sunlight showed significant decrease in the response for higher dose at 588 and 510 nm and slower decrease
in the response for lower dose at the above mentioned wavelengths. However the response was almost stable up to 97 days at
460 nm for higher and lower doses. At 4 °C, the decrease in the absorbance was slower at 588 and 510 nm while the response
was almost constant at 460 nm. At higher temperatures, such as 40 °C, the decrease in the absorbance was greater at 588 and
510 nm while at 460 nm the absorbance was almost constant for about 3 months. 相似文献
110.
Armstrong TA Bettoni D Bharadwaj V Biino C Borreani G Broemmelsiek D Buzzo A Calabrese R Ceccucci A Cester R Church M Dalpiaz P Dalpiaz PF Dimitroyannis D Fabbri M Fast J Gianoli A Ginsburg CM Gollwitzer K Govi G Hahn A Hasan M Hsueh S Lewis R Luppi E Macrí M Majewska AM Mandelkern M Marchetto F Marinelli M Marques J Marsh W Martini M Masuzawa M Menichetti E Migliori A Mussa R Palestini S Pallavicini M Passaggio S Pastrone N Patrignani C Peoples J Petrucci F Pia MG Pordes S Rapidis P Ray R 《Physical review D: Particles and fields》1996,54(11):7067-7070