SYNTHESIS OF 3,4-DIPHENYL-1.3,4-DIAZAPHOSPHOLID1N-2-ONE-4-OXIDE BY MANNICH-TYPE REACTION

Phenylurea reacted with dichlorophenylphosphine and aldehydes or ketones by Mannich-type reaction in anhydrous benzene to give five-mem- bered phosphorous heterocyclic compounds.However.derivatives of α-ureidoalkylphosphonic acids were obtained as the reaction performed in glacial acetic acid.

Photo-induced Coupling Reaction of 1,1-Diphenyl-2,2-dicyanoethylene with 10-Methyl-9,10-dihydroacridine

Diphenyl-2, 2-dicyanoethylene reacts with 10-methyl-9, 10-dihydroacridine in deaerated acetonitrile under irradiation with l>320 nm to give the coupling product 1, 1-diphenyl-1-(10-methyl-9-acridinyl)-2, 2-dicyanoethane, which has been characterized by X-ray crystallographic, MS and NMR analyses.

Evaluation of antioxidant activity of marine Agrobacterium SP. 1202

The three water-soluble polysaccharides （PI, PII and Pill）, the ethyl acetate extraction （EA） and its five fractions of petroleum ether （PeF）, ethyl acetate （EaF）, butanol （BuF）, methanol （MeF） and water （WtF） from marine agrobacterium 1202 were prepared and then subjected to antioxidant activity evaluation. The antioxidant activity was tested using the 1, 1-Diphenyl-2-picryl-hydrazyl （DPPH） free radical-scavenging assay, the hydrogen peroxide-induced luminot chemiluminescence （CL） assay and hydroxyl free radical-initiated chemiluminescence （CL） assay. All the fractions exerted significant inhibitory effects on hydrogen peroxide and hydroxyl free radical. The extracts of EA, EaF and BuF could also showed inhibition on DPPH. Among of them, the extracts of EaF showed full of antioxidant activity on the three tested system. The result suggested that the marine agrobacterium 1202 is a potential source of natural antioxidantagent.

Synthesis and Crystal Structure of 1,2-Dis(1,3-diphenylpropan-2-yl)disulfane

A novel compound of 1,2-dis（1,3-diphenylpropan-2-yl）disulfane（C30H30S2,Mr=454.27）was synthesized in ethanol with 1,3-diphenyl-2-propanone as raw materials,giving high yield of product（90%）.Its structure was determined by IR,1H NMR,MS,elemental analysis and X-ray diffraction.The crystal belongs to monoclinic,space group C2 with a=18.727（3）,b=6.5179（9）,c=13.7576（18）,β=131.0610（10）o,V=1266.2（3）3,Z=2,Dc=2.136 g/cm3,μ=1.078 mm-1,F（000）=843,R=0.0490 and wR=0.1247 for 3211 observed reflections with I2（I）.X-ray analysis reveals that the molecule is not symmetrical.There exist no classical hydrogen bonds andπ-πstacking interactions.Moreover,the thermal stability of compound 3 was investigated.

Antioxidant Activity Evaluation in a Series of Heterocyclic Compounds Derived from 1,8-Diaminonaphthalene

From (2,3-dihydro-1H-perimidin-2-yl)-phenyl, the substitution of OH group in ortho or para position on the phenyl ring, allows us to synthesize the studied compounds. These three compounds have been characterized by conventional spectroscopic methods (NMR and MS). The interest of this work is to review the antioxidant activity of our compounds. The antioxidant activity screening carried out according to FRAP and DPPH methods revealed significant anti-free radical properties for compounds 1 and 2 even at low concentrations. In contrast to the compound 2, compound 3 for which the OH group is substituted in para position has the lowest activity in both cases. Therefore the para position seems to be the least sensitive position to increase the antioxidant activity of this pharmacophore.

Morphology Control over the Organic Nanoparticles of 1,3-Diphenyl-5-(9-anthryl)-2-pyrazoline

The organic nanoparticles of a blue-light-emitting molecule,1,3-diphenyl-5-(9-anthryl)-2-pyrazoline,were prepared by reprecipitation method using acetonitrile as the solvent for the molecular precursor. Three morphologies,spherical,doughnut-shaped and cubic,could be observed on the silicon substrate for the nanoparticles by the volume-controlled addition of acetonitrile. The evolution of particle morphology as a function of acetonitrile addition was attributed to the variation of the growth habits of the particles in the different environment. The nanoparticles exhibit the novel photoluminescence spectra as compared to those of monomer and the bulk crystals.

药桑椹花青素的体外抗氧化作用

研究药桑椹花青素(anthocyanins from Morus nigra L.,AMNL)的体外抗氧化作用,并与白桑椹花青素(anthocyanins from Morus alba L.,AMAL)和黑桑椹花青素(anthocyanins from Morus alba Linn.var.tatarica,AMALV)的体外抗氧化作用进行比较。以芦丁和VC为对照,测定AMNL对二苯代苦味酰肼自由基(DPPH自由基)、超氧阴离子自由基(O2.)、羟自由基(.OH)和烷基自由基的清除能力,同时测定其体外总抗氧化能力。结果表明,AMNL对DPPH自由基的清除能力(IC50=9.07mg/L)显著高于AMAL与AMALV,弱于芦丁和VC。AMNL对O2.(IC50=2.82mg/L)和.OH(IC50=7.77mg/L)的清除能力不仅明显高于AMAL与AMALV,而且清除效果也优于芦丁和VC。各桑椹花青素对烷基自由基清除率均低于50%。AMNL总抗氧化能力分别是AMAL、AMALV及芦丁的11.8倍、2.6倍及1.3倍,但低于VC。

Effect of Induced Mutation on Antioxidant Activity in Ocimum basilicum Linn

Five batches from the same stock of seeds of Ocimum basilicum were irradiated at 5, 10, 15, 20 and 25 Gy, respectively using 60C source. Methanolic leaf extracts of these samples and a control were evaluated for their antioxidant activity by the 1,1-diphenyl-2-picryl-hydrazyl (DPPH) free radical scavenging method using M2 plants. All the methanolic extracts showed antioxidant activity. The IC50 of the methanolic extracts of the six different treatments, control, 5 Gy, 10 Gy, 15 Gy, 20 Gy and 25 Gy, showed antioxidant activity with IC50 values of 100, 90, 86, 61, 71 and 70 μg/ml, respectively. Three individual mutants, M-15-5, M-20-6 and M-15-4, had IC50 values of 26, 30 and 40 μg/ml, respectively. These mutants were from the 15 Gy and 20 Gy treatments. From the results, it is confirmed that induced mutation can be employed to create variation in the levels of free radical scavenging activity in O. basilicum and can therefore serve as a tool for breeding for high levels of antioxidant activity in O. basilicum.

一点红提取物体外抗氧化活性研究

目的:研究一点红提取物体外抗氧化活性。方法:通过水提醇沉、有机溶剂萃取、大孔树脂吸附纯化,得到六种不同部位的样品。以抗坏血酸和2,6-二叔丁基-4-甲基苯酚为对照,测定样品对羟基自由基和二苯基苦基苯肼自由基的清除能力,对Fe3+的还原能力,抑制油脂的氧化能力。结论:上述样品均具有一定的抗氧化活性,其中大孔树脂纯化的50%乙醇洗脱部位活性最好,但总体上弱于抗坏血酸和2,6-二叔丁基-4-甲基苯酚。

Synthesis of a New β-Mercaptoalcohol

In this letter, (R)-1,1-diphenyl-2-mercapto-3-methyl-1-butanol was synthesized from L-valine and two synthetic routes have been tried.

Comparison of Antioxidant Activities of Silver Nanoparticles and Methanol Extracts of Three Indigenous Nigeria Herbal Seeds

The antioxidant of seeds was carried out using extracts from methanol and Silver Nanoparticles from the spice. The SEM shows the shapes, dispersion and agglomeration of the sample, while the EDX confirms the SEM and the presence of some compounds. The FT-IR reveals the AgNPs capping and reducing the particular biomolecule from the functional group for identification. Compounds found in the FT-IR seeds of Capsicum annum are Ag L (Silver iodide), C K (Cyanogen chloride), P K (Phenol). Monodora myristica are Mo L (Molybdenum), Ag L (Silver iodide), C K (Cyanogen chloride), P K (Phenol), Mg K (Magnesium). Piper guineense are Ag L (Silver iodide), Ci K (Potassium chloride), C K (Cyanogen chloride), P K (Phenol). The seeds show that the AgNPS of CA and MM has a better antioxidant activity than the methanol of CA and MM, while the PG methanol has a better activity than the AgNPS PG. The control (Catechin and Galic acid) has a slight overall better DPPH activity than the AgNPS. It is important to note that there is a concentration dependency in CA, MM AgNPS, PG methanol respectively. Notably, at CA methanol, the conc. at 125 was higher than the conc. at 250. Hence, there is need to create a great part in using plant samples for making tabulated or capsulated drugs for treatment of diseases and using plant silver nanoparticles to develop a healthy food/drug preservative package material “smart packaging” that will enhance shelf-life.

A Comparative Study of Antioxidant Activities between Fresh and Dry Mushrooms in the Genera <i>Cantharellus</i>and <i>Afrocantharellus</i>from Tanzania

Cantharellus and Afrocantharellus mushrooms are widely consumed in both fresh and dry forms. However, their antioxidant and whether their values changing with drying processes are not known. This study establishes their values and the effect of sun drying on their quality and quantity. Methanolic extracts of five Cantharellus and two Afrocantharellus species were investigated. The investigation used (1,1-diphenyl-2-picrylhydrazyl radical) DPPH as a substrate to determine radical scavenging abilities. Further quantitative analyses for carotenoids, flavonoid, total phenolic compounds and vitamin C content were done using spectrophotometric assay at 515 nm. Comparatively, fresh mushroom had higher vitamin C and Lycopene contents than their dry counterparts with β-carotene. Flavonoid and phenolic compounds were higher in dry forms than those in their fresh counterparts. Radical scavenging ability also varied with fresh forms depicting higher activity compared to dry forms. The variation was low in Afrocantharellus species (0.8% and 0.99%) while it was higher in Cantharellus species (24.12% and 7.52%). The highest ability was observed in fresh forms of Cantharellus pseudocibarius (EC50 50 = 0.4 mg/ml) was from dry form of Cantharellus rufopunctatus. This shows that studied mushrooms are rich in antioxidants and their quality and quantities are affected differently in both forms. Both dry and fresh mushrooms are potential sources of natural antioxidants. The portrayed high scavenging ability by these mushrooms envisages promoting them into potential nutraceutics.

Synthesis of 3,3,5,5-tetrabenzyl-1,2,4-trithiol and 1,2-dis(1,3-arylpropan-2-yl)disulfane

Novel sulfur-containing compounds （3a-3c, 4a-4c） were obtained in ethanol with 1,3-diphenyl-2- propanone as the starting material. The advantages of this procedure were mild reaction conditions, simple protocol, and high yields. The structures of the products were characterized by IR, 1H NMR, MS and elementary analysis. The crystal of the new compound 4a belongs to monoclinic, space group C2 with a=18.727（3）, b=6.5179（9）, c=13.7576（18） A, fl=131.0610（10）°, V=I266.2（3）A3, Z=2, Dc=2.136g/cm3, μ=1.078mm 1, F（000）=843, R=0.0490 and wR=0.1247 for 3211 observed reflection with I 〉 2σ（I）. X-ray analysis reveals that the molecule is not symmetrical, the molecular structure is stabilized by weak π-π stacking interactions, and no classical hydrogen bonds can be observed.

The Application of Novel Electrochemical Approach to Antioxidant Activity Assay of Metal Porphyrins with Bulky 3,5-Diisobornyl-4-hydroxyphenyl Moieties

The complexes of biogenic metals (Zn2+,Cu2+,Co2+,Mn3+,Fe3+) based on meso-tetra(3,5-diisobor- nyl-4-hydroxyphenyl)porphyrin 1 were synthesized. The electrochemical behavior of these com-pounds was studied using cyclic voltammetry (CV) and rotating disk electrode (RDE) techniques. The antioxidant activity of complexes was estimated by means of the electrochemical assay based on the hydrogen atom transfer reaction to the stable radical 2,2’-diphenyl-1-picrylhydrazyl (DPPH). The RDE method was applied for this process monitoring. It was shown that the efficiency of the metal complexes (Cu2+,Co2+,Mn2+,Ni2+,Fe3+) is practically the same order as that of free base porphyrin 1. However the Zn2+ complex demonstrates significantly higher antioxidant activity, and the stoichiometry of the reaction was determined as σ = 4. The results demonstrate that porphyrin macrocycle can directly affect the antioxidant properties of 2,6-diisobornylphenol.

草珊瑚药材抗氧化活性化学成分研究

采用有机溶剂萃取和多种色谱技术从林下种植的草珊瑚药材中分离具有抗氧化活性的化学成分,再根据其波谱数据和理化性质进行结构鉴定,并采用体外1,1-二苯基-2-苦基肼(DPPH)抗氧化模型进行化学成分抗氧化活性评价.结果首次从草珊瑚药材中分离到2个黄酮类化合物cilicicone B(1)和β,2,3',4,4',6-六羟基-α-(α-L-吡喃鼠李糖基)-二氢查耳酮(2),经DPPH自由基清除实验表明化合物1和2具有较强的抗氧化活性,化合物1能清除DPPH的质量值为4.16,化合物2的ρIC50值为2.15.