A new phloretin derivative 1 3-[2-(4-hydroxy-phenyl)-ethyl]-benzo[d] isoxazole-4,6-diol (yield 63%) was synthesized from phloretin by carbonyl nucleophilic addition condensation reaction. Its structure was characteriz...A new phloretin derivative 1 3-[2-(4-hydroxy-phenyl)-ethyl]-benzo[d] isoxazole-4,6-diol (yield 63%) was synthesized from phloretin by carbonyl nucleophilic addition condensation reaction. Its structure was characterized by 1H NMR, 13C NMR and HR-MS. The phloretin, compound 1, resveratrol and acetylated resveratrol were determined by comparing them with paclitaxel. Anti-tumor activity of alcohol on SPC-A1, EC109, A549, MCF-7 and MDA-MB-231 cell lines. Compound 1 showed better antitumor activity than docetaxel against A549 tumor cells.展开更多
The effect of 2-butyne-1, 4-diol （BD） on the deposition behavior of the Co-Ni alloy was investigated by linear sweep voltammetry. The results showed that BD could prevent the deposition of the Co-Ni alloy. The effec...The effect of 2-butyne-1, 4-diol （BD） on the deposition behavior of the Co-Ni alloy was investigated by linear sweep voltammetry. The results showed that BD could prevent the deposition of the Co-Ni alloy. The effect of BD concentration in the sulfate plating bath, on the structure of the Co-Ni deposit was studied by energy dispersive x-ray spectroscopy, scanning electron microscope, and X-ray diffraction, respectively. As a result, BD could smoothen the deposit surface and decrease the diameter of the grain, but too much of BD was not good for the size of the grain. In general, a hexagonal close-packed （hcp） phase of the Co-Ni alloy, with a preferentially oriented （110） plane, was prepared by electrodeposition in the presence of BD. The Co-Ni alloy as a catalyst for the electro-oxidation of ethanol in alkaline medium was investigated by cyclic voltammetry. The deposit plated from the bath containing BD possessed better electro-oxidation of ethanol performance compared with that of the deposit plated from only the sulfate plating bath, but too much of BD was not beneficial for catalytic activity. The Co-Ni film was suitable as a magnetic recording material.展开更多
The effect of 2-butyne-1, 4-diol on silver electrodeposition process from 5, 5-dimethyl hydantoin solutions was investigated by means of cyclic voltammetric measurement, scanning electron microscopy (SEM) and X-ray di...The effect of 2-butyne-1, 4-diol on silver electrodeposition process from 5, 5-dimethyl hydantoin solutions was investigated by means of cyclic voltammetric measurement, scanning electron microscopy (SEM) and X-ray diffraction (XRD). Cyclic voltammetric studies indicate that the reduction process of silver electrodeposition is influenced by adding 2-butyne-1, 4-diol. Owing to its adsorption on the electrode surface, 2-butyne-1, 4-diol moderately hinders the mass transfer of the silver complexed ions from the bulk solution to the outer limit of the electrode double layer and affects the electrocrystallization step. Scanning electron microscopy analysis reveals that the presence of 2-butyne-1, 4-diol in the electrolyte is beneficial and the silver deposits obtained are smoother, more compact and more leveled. X-ray diffraction analysis of the silver deposits obtained at 0.5 g·L-1 2-butyne-1, 4-diol indicated that the (110) plane is the most preferred plane and is not affected by the presence of 2-butyne-1, 4-diol in the electrolyte.展开更多
Objective:To evaluate the in-vitro antioxidant and antimicrobial activity of cvcloart-23- ene-3β,25-diol(called as B2) isolated from stem bark of Pongamia pinnata.Methods:In vitro antioxidant activity of B2 was deter...Objective:To evaluate the in-vitro antioxidant and antimicrobial activity of cvcloart-23- ene-3β,25-diol(called as B2) isolated from stem bark of Pongamia pinnata.Methods:In vitro antioxidant activity of B2 was determined by methods for determination of Dl’PH radical scavenging,reducing power,superoxide anion radical scavenging,hydroxyl radical scavenging, hydrogen peroxide scavenging,metal chelating and nitric oxide radical scavenging at the doses of 20.40.60.80 and 100μg/mL,respectively.3 -tocopherol with same concentration was used as a standard antioxidant.In vitro antimicrobial activity of B2 was determined by cup plate method in different concentration range of 10-100μg/mL.Results:The results indicated that dose dependent%reduction against DPPH radical,reducing power,superoxide anion radical scavenging,hydroxyl radical scavenging,metal chelating,hydrogen peroxide scavenging and nitric oxide radical scavenging by B2 andβ-tocopherol.Conclusions:It is concluded that cycloart 23-ene-3β,25 diol(B2) showed dose dependent antioxidant activity.B2 showed more DPPH radical scavenging,reducing power,superoxide scavenging,hydroxyl radical scavenging, metal chelating scavenging,hydrogen peroxide radical scavenging and nitric oxide radical scavenging activity thanβ-tocopherol and in case of antimicrobial activity B2 exhibited broad-spectrum activ ity against bacteria and strong activity against yeast type of fungi.展开更多
Objective: To investigate the effects of friedelin(terpenoid) and 8-hydroxyisocapnolactone-2-3-diol(coumarin) with concentration 10 mM, 30 m M, and 100 mM on inhibiting mast cells(MCs) degranulation.Methods: The inves...Objective: To investigate the effects of friedelin(terpenoid) and 8-hydroxyisocapnolactone-2-3-diol(coumarin) with concentration 10 mM, 30 m M, and 100 mM on inhibiting mast cells(MCs) degranulation.Methods: The investigation was performed in vitro by administering each compound into rat peritoneal MCs and rat basophilic leukemia-2 H3 cells followed by activation with50 mg/m L of compound 48/80 or 1 m M of ionomycin. The concentration of histamine released from each group was measured by a high-performance liquid chromatographyfluorometry system with post-column derivatization using o-phthalaldehyde.Results: 8-Hydroxyisocapnolactone-2-3-diol inhibited degranulation of compound 48/80 activated-rat peritoneal MCs with the histamine release percentages of 74.57%,72.21% and 51.79% when the 10 mM, 30 m M and 100 mM concentrations were used,respectively. Where as about 81% histamine was released by the control group.Degranulation inhibition ability was also observed in ionomycin-activated rat basophilic leukemia-2 H3 cells. In contrast, friedelin failed to inhibit degranulation in either cell type.The inhibition of 8-hydroxyisocapnolactone-2-3-diol was not related to the depletion of histamine synthesis as implied by the total histamine measurement.Conclusions: These results exhibit the promising of 8-hydroxyisocapnolactone-2-3-diol is a potential parent structure for developing a MCs stabilizer.展开更多
The cis and trans isomers separation of 2-butene-1,4-diol and lafutidine were studied by HPLC on two kinds of chiral columns: (S,S)-Whelk-O 1 and ChiraSpher. The isomers of 2-butene-1,4-diol can be separated on both c...The cis and trans isomers separation of 2-butene-1,4-diol and lafutidine were studied by HPLC on two kinds of chiral columns: (S,S)-Whelk-O 1 and ChiraSpher. The isomers of 2-butene-1,4-diol can be separated on both chiral columns while the isomers of lafutidine can only be resolved on ChiraSpher column. The influence of different type and amount of mobile phase modifier on the isomers separation was extensively studied. The resolution of cis and trans isomers of 2-butene-1,4-diol was 2.61on (S,S)-Whelk-O 1 column with hexane-ethanol (97:3, v/v) as the mobile phase. The resolution of lafutidine was 1.89 on ChiraSpher column with hexane-ethanol-THF-diethylamine (92:3:5:0.1, v/v/v/v) as the mobile phase. LC-MS methods were developed to identify the isomer peaks.展开更多
2-Acetyl-5-methyl-2H-1,2,3—diaraphosphole 1 reacted with 2—butyne—1, 4—diol to form a tricoordinated phosphorus compound 7, which then rearranged to a novel 2, 3-disubstituted-1, 3-diene.Similar rearrangement has ...2-Acetyl-5-methyl-2H-1,2,3—diaraphosphole 1 reacted with 2—butyne—1, 4—diol to form a tricoordinated phosphorus compound 7, which then rearranged to a novel 2, 3-disubstituted-1, 3-diene.Similar rearrangement has been observed when diphenylchloropbosphine reacted with 2-butyne—1,4-diol展开更多
文摘A new phloretin derivative 1 3-[2-(4-hydroxy-phenyl)-ethyl]-benzo[d] isoxazole-4,6-diol (yield 63%) was synthesized from phloretin by carbonyl nucleophilic addition condensation reaction. Its structure was characterized by 1H NMR, 13C NMR and HR-MS. The phloretin, compound 1, resveratrol and acetylated resveratrol were determined by comparing them with paclitaxel. Anti-tumor activity of alcohol on SPC-A1, EC109, A549, MCF-7 and MDA-MB-231 cell lines. Compound 1 showed better antitumor activity than docetaxel against A549 tumor cells.
基金Financial Support by the National Natural Science Foundation of China (No.29872016) the Hong Kong Polytechnic University ASD Fund are gratefully acknowledged.
基金supported by the Natural Science Foundation of Fujian Province,China(Grant No.2006J0440).
文摘The effect of 2-butyne-1, 4-diol （BD） on the deposition behavior of the Co-Ni alloy was investigated by linear sweep voltammetry. The results showed that BD could prevent the deposition of the Co-Ni alloy. The effect of BD concentration in the sulfate plating bath, on the structure of the Co-Ni deposit was studied by energy dispersive x-ray spectroscopy, scanning electron microscope, and X-ray diffraction, respectively. As a result, BD could smoothen the deposit surface and decrease the diameter of the grain, but too much of BD was not good for the size of the grain. In general, a hexagonal close-packed （hcp） phase of the Co-Ni alloy, with a preferentially oriented （110） plane, was prepared by electrodeposition in the presence of BD. The Co-Ni alloy as a catalyst for the electro-oxidation of ethanol in alkaline medium was investigated by cyclic voltammetry. The deposit plated from the bath containing BD possessed better electro-oxidation of ethanol performance compared with that of the deposit plated from only the sulfate plating bath, but too much of BD was not beneficial for catalytic activity. The Co-Ni film was suitable as a magnetic recording material.
文摘The effect of 2-butyne-1, 4-diol on silver electrodeposition process from 5, 5-dimethyl hydantoin solutions was investigated by means of cyclic voltammetric measurement, scanning electron microscopy (SEM) and X-ray diffraction (XRD). Cyclic voltammetric studies indicate that the reduction process of silver electrodeposition is influenced by adding 2-butyne-1, 4-diol. Owing to its adsorption on the electrode surface, 2-butyne-1, 4-diol moderately hinders the mass transfer of the silver complexed ions from the bulk solution to the outer limit of the electrode double layer and affects the electrocrystallization step. Scanning electron microscopy analysis reveals that the presence of 2-butyne-1, 4-diol in the electrolyte is beneficial and the silver deposits obtained are smoother, more compact and more leveled. X-ray diffraction analysis of the silver deposits obtained at 0.5 g·L-1 2-butyne-1, 4-diol indicated that the (110) plane is the most preferred plane and is not affected by the presence of 2-butyne-1, 4-diol in the electrolyte.
文摘Objective:To evaluate the in-vitro antioxidant and antimicrobial activity of cvcloart-23- ene-3β,25-diol(called as B2) isolated from stem bark of Pongamia pinnata.Methods:In vitro antioxidant activity of B2 was determined by methods for determination of Dl’PH radical scavenging,reducing power,superoxide anion radical scavenging,hydroxyl radical scavenging, hydrogen peroxide scavenging,metal chelating and nitric oxide radical scavenging at the doses of 20.40.60.80 and 100μg/mL,respectively.3 -tocopherol with same concentration was used as a standard antioxidant.In vitro antimicrobial activity of B2 was determined by cup plate method in different concentration range of 10-100μg/mL.Results:The results indicated that dose dependent%reduction against DPPH radical,reducing power,superoxide anion radical scavenging,hydroxyl radical scavenging,metal chelating,hydrogen peroxide scavenging and nitric oxide radical scavenging by B2 andβ-tocopherol.Conclusions:It is concluded that cycloart 23-ene-3β,25 diol(B2) showed dose dependent antioxidant activity.B2 showed more DPPH radical scavenging,reducing power,superoxide scavenging,hydroxyl radical scavenging, metal chelating scavenging,hydrogen peroxide radical scavenging and nitric oxide radical scavenging activity thanβ-tocopherol and in case of antimicrobial activity B2 exhibited broad-spectrum activ ity against bacteria and strong activity against yeast type of fungi.
文摘Objective: To investigate the effects of friedelin(terpenoid) and 8-hydroxyisocapnolactone-2-3-diol(coumarin) with concentration 10 mM, 30 m M, and 100 mM on inhibiting mast cells(MCs) degranulation.Methods: The investigation was performed in vitro by administering each compound into rat peritoneal MCs and rat basophilic leukemia-2 H3 cells followed by activation with50 mg/m L of compound 48/80 or 1 m M of ionomycin. The concentration of histamine released from each group was measured by a high-performance liquid chromatographyfluorometry system with post-column derivatization using o-phthalaldehyde.Results: 8-Hydroxyisocapnolactone-2-3-diol inhibited degranulation of compound 48/80 activated-rat peritoneal MCs with the histamine release percentages of 74.57%,72.21% and 51.79% when the 10 mM, 30 m M and 100 mM concentrations were used,respectively. Where as about 81% histamine was released by the control group.Degranulation inhibition ability was also observed in ionomycin-activated rat basophilic leukemia-2 H3 cells. In contrast, friedelin failed to inhibit degranulation in either cell type.The inhibition of 8-hydroxyisocapnolactone-2-3-diol was not related to the depletion of histamine synthesis as implied by the total histamine measurement.Conclusions: These results exhibit the promising of 8-hydroxyisocapnolactone-2-3-diol is a potential parent structure for developing a MCs stabilizer.
文摘The cis and trans isomers separation of 2-butene-1,4-diol and lafutidine were studied by HPLC on two kinds of chiral columns: (S,S)-Whelk-O 1 and ChiraSpher. The isomers of 2-butene-1,4-diol can be separated on both chiral columns while the isomers of lafutidine can only be resolved on ChiraSpher column. The influence of different type and amount of mobile phase modifier on the isomers separation was extensively studied. The resolution of cis and trans isomers of 2-butene-1,4-diol was 2.61on (S,S)-Whelk-O 1 column with hexane-ethanol (97:3, v/v) as the mobile phase. The resolution of lafutidine was 1.89 on ChiraSpher column with hexane-ethanol-THF-diethylamine (92:3:5:0.1, v/v/v/v) as the mobile phase. LC-MS methods were developed to identify the isomer peaks.
文摘2-Acetyl-5-methyl-2H-1,2,3—diaraphosphole 1 reacted with 2—butyne—1, 4—diol to form a tricoordinated phosphorus compound 7, which then rearranged to a novel 2, 3-disubstituted-1, 3-diene.Similar rearrangement has been observed when diphenylchloropbosphine reacted with 2-butyne—1,4-diol
