Superwetting materials have drawn unprecedented attention in the treatment of oily wastewater due to their preferable anti-fouling property and selective oil/water separation.However,it is still a challenge to fabrica...Superwetting materials have drawn unprecedented attention in the treatment of oily wastewater due to their preferable anti-fouling property and selective oil/water separation.However,it is still a challenge to fabricate multifunctional and environmentally friendly materials,which can be stably applied to purify the actual complicated wastewater.Here,a Ag/Ag/α-Fe_(2)O_(3) heterostructure anchored copper mesh was intentionally synthesized using a facile two-step hydrothermal method.The resultant mesh with superhydrophilicity and underwater superoleophobicity was capable of separating various oil/water mixtures with superior separation efficiency and high permeationflux driven by gravity.Benefiting from the joint effects of the smaller band gap of Ag/α-Fe_(2)O_(3) heterojunction,inherent antibacterial capacity of Ag/α-Fe_(2)O_(3) and Ag nanoparticles,favorable conductive substrate,as well as the hierarchical structure with superwettability,such mesh presented remarkably enhanced degradation capability toward organic dyes under visible light irradiation and antibacterial activity against both Escherichia coli(E.coli)and Staphylococcus aureus(S.aureus)compared with the pure Ag/α-Fe_(2)O_(3) coated mesh.Impressively,the mesh exhibited bifunctional water purification performance,in which organic dyes were eliminated simultaneously from water during oil/water separation in onefiltration process.More importantly,this mesh behaved exceptional chemical resistance,mechanical stability and long-term reusability.Therefore,this material with multifunctional integration may hold promising potential for steady water purification in practice.展开更多
Starting from sissotrin (1), a natural isoflavonoid isolated from Trifolium baccarinii (Fabaceae), one new semisynthetic derivative, 6-nitrobiochanin A (1b) and two known derivatives, 8-nitrobiochanin A (1a) and 2&quo...Starting from sissotrin (1), a natural isoflavonoid isolated from Trifolium baccarinii (Fabaceae), one new semisynthetic derivative, 6-nitrobiochanin A (1b) and two known derivatives, 8-nitrobiochanin A (1a) and 2",3",4",6"-tetraacetylsissotrin (1c) have been obtained after performing nitration and acetylation reactions. Their structures were assigned after interpretation of their spectrometric (HR-ESI-MS) and spectroscopic (NMR 1D and 2D) data and by comparison with those reported in the literature. The substrate as well as the semisynthetic derivatives were evaluated for their antibacterial activities against six strains. The results reveal that they are inactive or weakly active on the strains tested with the exception of 8-nitrobiochanin A (1a) which showed moderate activity (MIC = 62.5 μg∙mL<sup>−1</sup>) on Staphylococcus aureus ATCC 43300.展开更多
[Objectives]To investigate the antioxidant,anti-inflammatory and antibacterial activities of different extracts(aqueous,ethanol,ethyl acetate and n-butanol extracts)of Miao medicine Polygonum capitatum.[Methods]Eleven...[Objectives]To investigate the antioxidant,anti-inflammatory and antibacterial activities of different extracts(aqueous,ethanol,ethyl acetate and n-butanol extracts)of Miao medicine Polygonum capitatum.[Methods]Eleven batches of P.capitatum in Guizhou province were collected,and water,ethanol,ethyl acetate and n-butanol extracts were prepared by reflux extraction.Antioxidant activity was determined by radical scavenging capacity of 1,1 diphenyl-2-picyl hydrazine(DPPH),anti-inflammatory activity was screened by lipopolysaccharide(LPS)induced RAW264.7 cells to produce NO,and the minimum inhibitory concentration(MIC)was screened by broth microdilution method.[Results]When the concentration of ethyl acetate extract was 10 mg/L,the scavenging rate of DPPH ranged from 90%to 99%.The(MIC of the ethyl acetate extract against Staphylococcus aureus(SA),Pseudomonas aeruginosa(PA)and Escherichia coli(EC)was 0.18-0.65,0.13-0.82,and 0.15-0.78 g/L,respectively.In the anti-inflammatory activity,ethyl acetate extract inhibited NO production with inhibition rate of 70%.[Conclusions]The ethyl acetate extract and ethanol extract of Miao medicine P.capitatum have strong antioxidant,anti-inflammatory and antibacterial activities.展开更多
Two new zinc(Ⅱ) complexes, [Zn2L2Ch].2[ZnL(CH3OH)Cl2] 1 and [ZnL2(NO3)2] 2, were synthesized by reacting ZnX2.nH2O (X = Cl^-, NO3^-) and a Schiff base ligand 2-[(4-methylphenylimino)methyl]-6-methoxyphenol ...Two new zinc(Ⅱ) complexes, [Zn2L2Ch].2[ZnL(CH3OH)Cl2] 1 and [ZnL2(NO3)2] 2, were synthesized by reacting ZnX2.nH2O (X = Cl^-, NO3^-) and a Schiff base ligand 2-[(4-methylphenylimino)methyl]-6-methoxyphenol (C15HIsNO2, L) which was obtained by the condensation of o-vanillin (2-hydroxy-3-methoxybenzaldehyde) with p-toluidine. Both 1 and 2 were characterized by single-crystal X-ray diffraction technique, elemental analysis, molar conductance, FT-IR, UV-Vis, IH-NMR spectra and thermogravimetrie analysis. The Schiff base ligand and its zinc(Ⅱ) complexes have been tested in vitro to evaluate their antibacterial activity against bacteria, viz., Escherichia Coli, Staphylococcus aureus and Bacillus Subtilis. The results show that these complexes have higher activity than the corresponding free Schiff base ligand against the same bacteria.展开更多
A series of novel 7-(3-aminopyrrolo[3,4-c]pyrazol-5(2H,4H,6H)-yl)quinolone derivatives were designed, synthesized and evaluated for in vitro antibacterial activities. Compounds 6g, 7g and 7h with the potencies sim...A series of novel 7-(3-aminopyrrolo[3,4-c]pyrazol-5(2H,4H,6H)-yl)quinolone derivatives were designed, synthesized and evaluated for in vitro antibacterial activities. Compounds 6g, 7g and 7h with the potencies similar to those of gemifloxacin, moxifloxaein, gatifloxacin and levofloxacin against Gram-positive organisms, worth further investigation.展开更多
The title compound C15H12N4O2S was synthesized by the reaction of 3-(2-hydroxybenzyl)-4-amino-(1H)-1,2,4-triazole-5-thione with 4-hydroxybenzaldehyde in ethanol and characterized by IR, ^1H NMR spectra and element...The title compound C15H12N4O2S was synthesized by the reaction of 3-(2-hydroxybenzyl)-4-amino-(1H)-1,2,4-triazole-5-thione with 4-hydroxybenzaldehyde in ethanol and characterized by IR, ^1H NMR spectra and elemental analysis. Its structure has been determined by X-ray diffraction analysis. The crystal belongs to monoclinic, space group C2/c with a = 27.990(3), b = 13.1326(14), c = 7.9770(8) A, β= 105.787(2)°, V = 2821.6(5)A^3, Z = 8, Mr= 312.35,μ= 0.243 mm^-1, Dc = 1.471 g/cm^3 and F(000) = 1296. The structure was solved by direct methods.and refined to a Rint value of 0.0388. The crystal structure involving in intermolecular N-H…S and O-H…S hydrogen bonds is observed, meanwhile intramolecular O-H…N hydrogen bond is also found. Their biological activities have been measured. The results show that this type of compound has certain antibacterial activity for Staphylococous aureus and Bacillus subtilis.展开更多
The title compound, C9H9N5OS, was synthesized by the reaction of 3-(1H)-1,2,4 -triazole hydrazine with 3-methyl-2-thiophenecarboxaldehyde in ethanol. The single crystal structure has been determined by X-ray diffrac...The title compound, C9H9N5OS, was synthesized by the reaction of 3-(1H)-1,2,4 -triazole hydrazine with 3-methyl-2-thiophenecarboxaldehyde in ethanol. The single crystal structure has been determined by X-ray diffraction analysis. The crystal belongs to monoclinic system, space group P2 1/n with a = 9.5550(10), b = 11.9847(12), c = 10.1074(11) A,β= 112.995(2)° V= 1065.47(19) A^3, Z = 4,μ = 0.290 mm^-1, Mr= 235.27, Dc = 1.467 g/cm^3 and F(000) = 488. The structure was solved by direct methods and refined to R = 0.0449. The crystal structure involves intermolecular hydrogen bonds of N-H…O and N-H…N as well as intramolecular hydrogen bond of N-H…N. Its biological activity has also been determined showing this type of compounds has certain antibacterial activity.展开更多
Ten new erythromycin antibacterial agents containing amidino group were designed and synthesized from erythromycin via oximation, reduction and condensation. Their structures were confirmed by MS and 13C NMR; the synt...Ten new erythromycin antibacterial agents containing amidino group were designed and synthesized from erythromycin via oximation, reduction and condensation. Their structures were confirmed by MS and 13C NMR; the synthetic condition(reaction medium)was explored; and their in vtiro antibacterial activities were tested. Compound HMA-3 showed antibacterial activity against staphylococcus aureus, which is equivalent to that of erythromycin A. Compounds HMA-8 and HMA-4 also showed an antibacterial activitiy. But no compound showed bactericidal activity.展开更多
4-Methyl-2-(4-methylphenyl)-5-(2-thiazolinyl)-1,3-thiazole, a novel compound, was synthesized by the annulation of 5-hydroxyethylcarbamoyl-4-methyl-2-(4- methylphenyl)-1,3-thiazole with P2S5. 5-Hydroxyethylcarba...4-Methyl-2-(4-methylphenyl)-5-(2-thiazolinyl)-1,3-thiazole, a novel compound, was synthesized by the annulation of 5-hydroxyethylcarbamoyl-4-methyl-2-(4- methylphenyl)-1,3-thiazole with P2S5. 5-Hydroxyethylcarbamoyl-4-methyl-2-(4-methylphenyl)-1,3-thiazole was prepared from the starting material of p-tolunitrile. The newly synthesized compounds were characterized by elemental analysis, IR, NMR(^1H, ^13C) and MS spectra. Hence, the crystal of the title compound was obtained, and its structure was determined by X-ray diffraction analysis. The crystal belongs to the triclinic system, space group P1 with a = 7.354(4), b = 8.383(4), c = 11.543(6)A, α = 76.688(6), β = 72.299(6), γ = 88.157(6)°, V = 659.2(6) A^3, Z = 2, Mr = 274.39, Dc = 1.382 g/cm^3, μ = 0.386 mm^-1, F(000) = 288, R = 0.0586 and w R = 0.1808 for 2984 unique reflections with 2213 observed ones(I 〉 2σ(I)). The title compound was also screened for its antibacterial activities against Bacillus subtilis and Escherichia coli. The result indicates that the target compound presents potential antimicrobial activities, and that the minimum inhibitory concentration(MIC) values of the title compound against the two tested strains are both 62.5 μg/mL.展开更多
A new kind of Schiff base HL(HL= 1-phenyl-3-methyl-4-(p-methylbenzoyl)-5-pyrazolone with L-Leucine methyl ester) and complexes Ni L′_2·0.75C_2H_5OH·0.25H_2O,Cu L′′2(L′ = 1-phenyl-3-methyl-4-(p-meth...A new kind of Schiff base HL(HL= 1-phenyl-3-methyl-4-(p-methylbenzoyl)-5-pyrazolone with L-Leucine methyl ester) and complexes Ni L′_2·0.75C_2H_5OH·0.25H_2O,Cu L′′2(L′ = 1-phenyl-3-methyl-4-(p-methylbenzoyl)-5-pyrazolone with L-leucine ethyl,L′′ = 1-phenyl-3-methyl-4-(p-methylbenzoyl)-5-pyrazolone with L-leucine) have been synthesized and structurally determined by X-ray diffraction. For HL: crystal structure determination indicates that there are two independent HLs with different conformations in one asymmetric unit. For complex 1: the Ni(Ⅱ) ion is six-coordinated by two carbonyl oxygen atoms from pyrazolone ring,two nitrogen atoms from different HL′ and two oxygen atoms from L-Leucine ethyl ester to form a distorted octahedral geometry. For complex 2: the Cu(Ⅱ) ion is four-coordinated by one carbonyl oxygen atom from the pyrazolone ring,one nitrogen atom from HL′′,and two different carboxylic oxygen atoms from L-leucine with the same conformation to form a distorted quadrilateral geometry.展开更多
Nine novel erythromycin O-alkylamidoxime derivatives were prepared in excellent yields via the condensation of different O-alkylhydroxylamines with erythromycin imino ether. The structures of all the compounds prepare...Nine novel erythromycin O-alkylamidoxime derivatives were prepared in excellent yields via the condensation of different O-alkylhydroxylamines with erythromycin imino ether. The structures of all the compounds prepared were confirmed by ^1 H NMR, 13C NMR, IR and MS, and their in vtiro antibacterial activities were tested. Among the compounds, two of them showed good antibacterial aetivities.展开更多
The title compound C18H22N4O4 was synthesized by the reaction of 3-hydrazine-4-hydroxy-6-methyl-2(1H)-pyridinones with 2-hydroxy-4-diethylaminobenzaldehyde in ethanol and characteri- zed by IR, tH NMR and elemental ...The title compound C18H22N4O4 was synthesized by the reaction of 3-hydrazine-4-hydroxy-6-methyl-2(1H)-pyridinones with 2-hydroxy-4-diethylaminobenzaldehyde in ethanol and characteri- zed by IR, tH NMR and elemental analysis. The single-crystal structure has been determined by X-ray diffraction analysis. The crystal belongs to the triclinic system, space group P1^- with a = 10.1930(14), b = 12.5200(17), c = 15.1863(19) A, α= 96.292(3), β= 96.450(3), γ= 102.443(3)°, V= 1862.6(4) A^3, Z= 4, Mr = 358.40, μ = 0.092 mm^-1, D c= 1.278 g/cm^3, F(000) = 760 and R = 0.0803. The crystal structure involves intermolcular N-H…O as well as intramolcular O-H…N, O-H…O and N-H…O hydrogen bonds. The title compound shows no antibacterial activity.展开更多
Two Schiff base complexes [Cu(L)2] (1) and [Zn(L)2]·3H2O(2) of (E)-4-fluoro-2-((3-morpholino propylimino)methyl)phenol (HL) have been synthesized and characterized by elemental analysis and single...Two Schiff base complexes [Cu(L)2] (1) and [Zn(L)2]·3H2O(2) of (E)-4-fluoro-2-((3-morpholino propylimino)methyl)phenol (HL) have been synthesized and characterized by elemental analysis and single-crystal X-ray diffraction. Crystal data for 1: triclinic, space group Pī with a=4.8000(10), b=11.109(2), c=13.921(3),α=66.55(3),β=80.35(3),γ=81.09(3)°, V=668.2(2)3 , Z=1, Dc=1.477g/cm 3 , F(000)=311, and the final R=0.0744 and wR=0.1601 for 2301 observed reflections with I 〉 2σ(I). And those for 2: monoclinic, space group P21 /c with a=14.789(3), b=11.713(2), c=18.846(4),β=107.85(3)°, V=3107.4(11)3 , Z=4, D c=1.389 g/cm 3 , F(000)=1368, and the final R=0.0749 and wR=0.1348 for 5423 observed reflections with I 〉 2σ(I). Both 1 and 2 are four-coordinated complexes, with a square-planar geometry of copper(Ⅱ) in 1 and a slightly distorted tetrahedral geometry of zinc(Ⅱ) in 2. An asymmetric unit consists of only one half of a Cu ion and one L ligand in 1, while an asymmetric unit is composed of one Zn ion, two L ligands and three water molecules in 2. Non-classical C-H···O and C-H F hydrogen bonds play important roles in the formation of a 1D chain of 1, but O-H O and O-H N hydrogen bonds play dominant roles in the self-assembly of a 3D network of 2. The antibacterial activities of 1 and 2 against B. subtilis, S. aureus, S. faecalis, P. aeruginosa, E. coli and E. cloacae have been evaluated by MTT method.展开更多
The title compound C18H18N4OS has been synthesized by the reaction of 3-(2-hydroxy- benzyl)-4-amino-(1H)-1,2,4-triazole-5-thione with 4-isopropylbenzaldehyde in ethanol and characterized by IR, ^1H NMR spectra and...The title compound C18H18N4OS has been synthesized by the reaction of 3-(2-hydroxy- benzyl)-4-amino-(1H)-1,2,4-triazole-5-thione with 4-isopropylbenzaldehyde in ethanol and characterized by IR, ^1H NMR spectra and elemental analysis. Its structure was determined by X-ray diffraction analysis. The crystal belongs to monoclinic, space group P21/c with a = 11.605(2), b = 7.401(1), c = 20.339(2) A, β= 103.05(2)°, V= 1701.8(4) A^3, Z = 4, Mr = 338.42,μ = 0.202 mm^-1, Dc = 1.321 g/cm^3 and F(000) = 712. The structure was solved by direct methods and refined to R = 0.0428 and wR = 0.1069. Due to the intramolecular O-H…N hydrogen bond and π-π stacking interactions between the benzene (C(1)~C(6)) and triazole rings, the two planes are essentially coplanar. Their biological activities have been measured, showing this type of compound has certain antibacterial activity for Staphylococous aureus and Bacillus subtilis. Based on the quantum chemistry calculation at the RHF/6-31G level, the frontier orbitals and electrostatic potential of the title compound were also discussed.展开更多
In the ethanol solvent, a nickel(Ⅱ) complex Ni(C12H10N2O2S)2 upon reaction of 2'-(2-thienylidene)-hydroxybenzoylhydrazide with nickel acetate was synthesized, and its structure was characterized by IR, UV, ele...In the ethanol solvent, a nickel(Ⅱ) complex Ni(C12H10N2O2S)2 upon reaction of 2'-(2-thienylidene)-hydroxybenzoylhydrazide with nickel acetate was synthesized, and its structure was characterized by IR, UV, elemental analysis and X-ray diffraction analysis. The crystal belongs to monoclinic system, space group C2/c with a = 22.052(3), b = 5.9681(6), c = 18.522(2)A , β = 110.679(4)°, V = 2280.6(4)A^3, Z = 4, Mr = 551.27, μ = 1.606 mm^-1, Dc = 1.075 g/cm^3, F(000) = 1136 and Rint = 0.0556. The nickel(Ⅱ ) atom in the compound is four-coordinated with two nitrogen atoms from amide and two oxygen atoms from keto group. The biological activities have been measured, show- ing the compound exhibits better anti-bacterial activity than the ligand.展开更多
The chemical study of <i>Rumex</i> <i>abyssinicus</i> Jacp (Polygonaceae) led to the iso<span>lation of a new ceramide named</span> (<i>R</i>)-2</span><span sty...The chemical study of <i>Rumex</i> <i>abyssinicus</i> Jacp (Polygonaceae) led to the iso<span>lation of a new ceramide named</span> (<i>R</i>)-2</span><span style="font-family:"">'</span><span style="font-family:"">-hydroxy-<i>N</i>-[(2<i>S</i>,3<i>S</i>,4<i>R</i>,16<i>E</i>)-1,3,4-trihy<span>droxyhexacos-16-en-2-yl]hexadecanamide (rumexamide) (<b>1</b>) together with</span> sixteen known compounds: bis-(2-ethylhexyl) phthalate (<b>2</b>), chrysophanol (<b>3</b>), physcion (<b>4</b>), citreorosein (<b>5</b>), emodin (<b>6</b>), chrysophanein (<b>7</b>), physcionin (<b>8</b>), <span>lupeol (<b>9</b>), 3<i>β</i>,28-dihydroxylup-20(29)-ene (<b>10</b>), 3<i>β</i>-dihydroxylup-</span>20(29)-en-28-oic acid (<b>11</b>), oleanolic acid (<b>12</b>), ergosta-6,22-diene-3,5,8-triol (<b>13</b>), stigmastane-3,6-dione (<b>14</b>), a mixture of <i>β</i>-sitosterol (<b>15</b>) and stigmasterol (<b>16</b>), and <span>stigmasterol 3-<i>O</i>-<i>β</i>-<i>D</i>-glucoside (<b>17</b>). Their structures were determined by </span>in<span>terpretation of their spectroscopic 1D NMR (<sup>1</sup>H and <sup>13</sup>C NMR), 2D NMR</span> (COSY <sup>1</sup>H-<sup>1</sup>H, HSQC and HMBC) data in conjunction with mass spectrometry<span> </span>(TOFESIMS and HR-TOFESIMS) and by comparison with those reported in the literature. Among all the known compounds, twelve <b>(2</b>, <b>5</b>, <b>8</b></span><b><span style="font-family:"">-</span></b><b><span style="font-family:"">17) </span></b><span style="font-family:"">were firstly isolated from <i>Rumex</i> <i>abyssinicus</i>, seven <b>(2, 10</b></span><b><span style="font-family:"">-</span></b><b><span style="font-family:"">14 and 17)</span></b><span style="font-family:""> from the genus <i>Rumex</i> and three (<b>13, 14, 17</b>) from family Polygonaceae. The <i>in</i> <i>vitro</i> antibacterial activities of extracts (MeOH, <i>n</i>-BuOH and EtOAc)</span><span style="font-family:"">,</span><span style="font-family:""> as well as compounds <b>9</b>, <b>11, 12</b>, <b>15</b></span><b><span style="font-family:""> </span></b><b><span style="font-family:"">+</span></b><b><span style="font-family:""> </span></b><b><span style="font-family:"">16</span></b><span style="font-family:""> and <b>17 </b>against pathogenic bacteria (<i>Staphylococcus</i> <i>aureus</i> ATCC 43300, <i>Shigella</i> <i>flexneri</i> NR 518, <i>Klebsiella</i> <i>pneumonia</i></span><i><span style="font-family:"">e</span></i><span style="font-family:""> ATCC 700603, <i>Escherichia</i> <i>coli</i> ATCC 25922)</span><span style="font-family:"">,</span><span style="font-family:""> were performed using </span><span style="font-family:"">the </span><span style="font-family:"">broth microdilution method and the results show that, extract</span><span style="font-family:"">s</span><span style="font-family:""> were not active (MIC </span><span style="font-family:"">></span><span style="font-family:""> </span><span style="font-family:"">1000 μg/mL) while compounds were weakly or not active (MIC ≥ 500 μg/mL) against all bacteria strains. Furthermore, the chemophenetic relationship</span><span style="font-family:"">s</span><span style="font-family:""> of the isolated compounds and their significance</span><span style="font-family:"">s</span><span style="font-family:""> were discussed.展开更多
A complex [NIL2] was synthesized, in which L, or to be exact, a Schiff base ligand (HL), was derived from the condensation of 1-phenyl-3-methyl-4-phenylacetyl-5-pyrazolone (PMPAP) with L-phenylalanine methyl ester...A complex [NIL2] was synthesized, in which L, or to be exact, a Schiff base ligand (HL), was derived from the condensation of 1-phenyl-3-methyl-4-phenylacetyl-5-pyrazolone (PMPAP) with L-phenylalanine methyl ester. They were characterized by IR and single-crystal X-ray diffraction. Green block crystals of both ligand and its complex were grown at room temperature. The ligand, which consists of two individual fragments, crystalizes in the P1 space group (a = 5.6268(5), b = 10.6892(11) and c = 19.4869(18) A). The complex crystalizes in the P21 space group (a -- 21.4076(18), b = 9.4792(8) and c = 25.287(2) A), which consists of a nickel six-coordinated compound. Every fragment is a distorted octahedron with four oxygen and two nitrogen atoms. The Schiff base ligand (HL) and its complex have been tested in vitro to evaluate their antibacterial activity against bacteria Escherichia Coli and Bacillus subtilis. It is found that the complex has higher activity than the corresponding free Schiff base ligand (HL) against the same bacterial.展开更多
A series of Benzisolselenazolone (BISA) derivatives were synthesized and evaluated for their antibacterial activities againstE coli. by using LKB-2277 bioactivity monitor. Other bioactivities were tested by the method...A series of Benzisolselenazolone (BISA) derivatives were synthesized and evaluated for their antibacterial activities againstE coli. by using LKB-2277 bioactivity monitor. Other bioactivities were tested by the method of High Throughput Screening for pharmaceutical activity compounds (HTP) BISA derivatives 3b, at the concentration of 40 μg/mL, showed 100%antibacterial activity and 62%inhibition rate of aldose reductase (at the concentration of 5μg/mL). These new compound structures have determined by IR,1H NMR and MS spectra.展开更多
基金This work was financially supported by the Shandong Provincial Natural Science Foundation(ZR2020QB116)the Excellent Young Talents Foundation in Universities of Anhui Province(gxyq2021223)the Key Research Project of Natural Science in Universities of Anhui Province.(KJ2020A0749).
文摘Superwetting materials have drawn unprecedented attention in the treatment of oily wastewater due to their preferable anti-fouling property and selective oil/water separation.However,it is still a challenge to fabricate multifunctional and environmentally friendly materials,which can be stably applied to purify the actual complicated wastewater.Here,a Ag/Ag/α-Fe_(2)O_(3) heterostructure anchored copper mesh was intentionally synthesized using a facile two-step hydrothermal method.The resultant mesh with superhydrophilicity and underwater superoleophobicity was capable of separating various oil/water mixtures with superior separation efficiency and high permeationflux driven by gravity.Benefiting from the joint effects of the smaller band gap of Ag/α-Fe_(2)O_(3) heterojunction,inherent antibacterial capacity of Ag/α-Fe_(2)O_(3) and Ag nanoparticles,favorable conductive substrate,as well as the hierarchical structure with superwettability,such mesh presented remarkably enhanced degradation capability toward organic dyes under visible light irradiation and antibacterial activity against both Escherichia coli(E.coli)and Staphylococcus aureus(S.aureus)compared with the pure Ag/α-Fe_(2)O_(3) coated mesh.Impressively,the mesh exhibited bifunctional water purification performance,in which organic dyes were eliminated simultaneously from water during oil/water separation in onefiltration process.More importantly,this mesh behaved exceptional chemical resistance,mechanical stability and long-term reusability.Therefore,this material with multifunctional integration may hold promising potential for steady water purification in practice.
文摘Starting from sissotrin (1), a natural isoflavonoid isolated from Trifolium baccarinii (Fabaceae), one new semisynthetic derivative, 6-nitrobiochanin A (1b) and two known derivatives, 8-nitrobiochanin A (1a) and 2",3",4",6"-tetraacetylsissotrin (1c) have been obtained after performing nitration and acetylation reactions. Their structures were assigned after interpretation of their spectrometric (HR-ESI-MS) and spectroscopic (NMR 1D and 2D) data and by comparison with those reported in the literature. The substrate as well as the semisynthetic derivatives were evaluated for their antibacterial activities against six strains. The results reveal that they are inactive or weakly active on the strains tested with the exception of 8-nitrobiochanin A (1a) which showed moderate activity (MIC = 62.5 μg∙mL<sup>−1</sup>) on Staphylococcus aureus ATCC 43300.
基金Supported by Science Foundation of Guizhou Education Technology(2022-064)Guizhou Provincial Science and Technology(ZK[2022]-362&[2022]4028)+2 种基金Science Foundation of Guizhou Health Commission(gzwkj2021-449)the Innovation and Entrepreneurship Training Program for Undergraduates from China(202210660131)Rural Economic Revitalization Research Project of Guizhou Medical University(GZYKDX-2022-002)。
文摘[Objectives]To investigate the antioxidant,anti-inflammatory and antibacterial activities of different extracts(aqueous,ethanol,ethyl acetate and n-butanol extracts)of Miao medicine Polygonum capitatum.[Methods]Eleven batches of P.capitatum in Guizhou province were collected,and water,ethanol,ethyl acetate and n-butanol extracts were prepared by reflux extraction.Antioxidant activity was determined by radical scavenging capacity of 1,1 diphenyl-2-picyl hydrazine(DPPH),anti-inflammatory activity was screened by lipopolysaccharide(LPS)induced RAW264.7 cells to produce NO,and the minimum inhibitory concentration(MIC)was screened by broth microdilution method.[Results]When the concentration of ethyl acetate extract was 10 mg/L,the scavenging rate of DPPH ranged from 90%to 99%.The(MIC of the ethyl acetate extract against Staphylococcus aureus(SA),Pseudomonas aeruginosa(PA)and Escherichia coli(EC)was 0.18-0.65,0.13-0.82,and 0.15-0.78 g/L,respectively.In the anti-inflammatory activity,ethyl acetate extract inhibited NO production with inhibition rate of 70%.[Conclusions]The ethyl acetate extract and ethanol extract of Miao medicine P.capitatum have strong antioxidant,anti-inflammatory and antibacterial activities.
文摘Two new zinc(Ⅱ) complexes, [Zn2L2Ch].2[ZnL(CH3OH)Cl2] 1 and [ZnL2(NO3)2] 2, were synthesized by reacting ZnX2.nH2O (X = Cl^-, NO3^-) and a Schiff base ligand 2-[(4-methylphenylimino)methyl]-6-methoxyphenol (C15HIsNO2, L) which was obtained by the condensation of o-vanillin (2-hydroxy-3-methoxybenzaldehyde) with p-toluidine. Both 1 and 2 were characterized by single-crystal X-ray diffraction technique, elemental analysis, molar conductance, FT-IR, UV-Vis, IH-NMR spectra and thermogravimetrie analysis. The Schiff base ligand and its zinc(Ⅱ) complexes have been tested in vitro to evaluate their antibacterial activity against bacteria, viz., Escherichia Coli, Staphylococcus aureus and Bacillus Subtilis. The results show that these complexes have higher activity than the corresponding free Schiff base ligand against the same bacteria.
基金supported by the National Major Science and Technology Project of China("Innovation and Development of New Drugs",No.2009ZX09301-003)
文摘A series of novel 7-(3-aminopyrrolo[3,4-c]pyrazol-5(2H,4H,6H)-yl)quinolone derivatives were designed, synthesized and evaluated for in vitro antibacterial activities. Compounds 6g, 7g and 7h with the potencies similar to those of gemifloxacin, moxifloxaein, gatifloxacin and levofloxacin against Gram-positive organisms, worth further investigation.
基金This work was supported by the Natural Science Foundation of Zhejiang Province (No. M203115) and Scientific Research Fund of Zhejiang Provincial Education Department (NO. 20050057)
文摘The title compound C15H12N4O2S was synthesized by the reaction of 3-(2-hydroxybenzyl)-4-amino-(1H)-1,2,4-triazole-5-thione with 4-hydroxybenzaldehyde in ethanol and characterized by IR, ^1H NMR spectra and elemental analysis. Its structure has been determined by X-ray diffraction analysis. The crystal belongs to monoclinic, space group C2/c with a = 27.990(3), b = 13.1326(14), c = 7.9770(8) A, β= 105.787(2)°, V = 2821.6(5)A^3, Z = 8, Mr= 312.35,μ= 0.243 mm^-1, Dc = 1.471 g/cm^3 and F(000) = 1296. The structure was solved by direct methods.and refined to a Rint value of 0.0388. The crystal structure involving in intermolecular N-H…S and O-H…S hydrogen bonds is observed, meanwhile intramolecular O-H…N hydrogen bond is also found. Their biological activities have been measured. The results show that this type of compound has certain antibacterial activity for Staphylococous aureus and Bacillus subtilis.
基金This work was supported by the Natural Science Foundation of Zhejiang Province (No. M203115) and Scientific Research Fund of Zhejiang Provincial Education Department(NO.20050057)
文摘The title compound, C9H9N5OS, was synthesized by the reaction of 3-(1H)-1,2,4 -triazole hydrazine with 3-methyl-2-thiophenecarboxaldehyde in ethanol. The single crystal structure has been determined by X-ray diffraction analysis. The crystal belongs to monoclinic system, space group P2 1/n with a = 9.5550(10), b = 11.9847(12), c = 10.1074(11) A,β= 112.995(2)° V= 1065.47(19) A^3, Z = 4,μ = 0.290 mm^-1, Mr= 235.27, Dc = 1.467 g/cm^3 and F(000) = 488. The structure was solved by direct methods and refined to R = 0.0449. The crystal structure involves intermolecular hydrogen bonds of N-H…O and N-H…N as well as intramolecular hydrogen bond of N-H…N. Its biological activity has also been determined showing this type of compounds has certain antibacterial activity.
文摘Ten new erythromycin antibacterial agents containing amidino group were designed and synthesized from erythromycin via oximation, reduction and condensation. Their structures were confirmed by MS and 13C NMR; the synthetic condition(reaction medium)was explored; and their in vtiro antibacterial activities were tested. Compound HMA-3 showed antibacterial activity against staphylococcus aureus, which is equivalent to that of erythromycin A. Compounds HMA-8 and HMA-4 also showed an antibacterial activitiy. But no compound showed bactericidal activity.
基金supported by the Open-end Funds of Jiangsu Key Laboratory of Marine Biotechnology,Huaihai Institute of Technology(2013HS004)Open-end Funds of Jiangsu Key Laboratory of Marine Pharmaceutical Compound Screening(2015HYB05)a project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions(201402)
文摘4-Methyl-2-(4-methylphenyl)-5-(2-thiazolinyl)-1,3-thiazole, a novel compound, was synthesized by the annulation of 5-hydroxyethylcarbamoyl-4-methyl-2-(4- methylphenyl)-1,3-thiazole with P2S5. 5-Hydroxyethylcarbamoyl-4-methyl-2-(4-methylphenyl)-1,3-thiazole was prepared from the starting material of p-tolunitrile. The newly synthesized compounds were characterized by elemental analysis, IR, NMR(^1H, ^13C) and MS spectra. Hence, the crystal of the title compound was obtained, and its structure was determined by X-ray diffraction analysis. The crystal belongs to the triclinic system, space group P1 with a = 7.354(4), b = 8.383(4), c = 11.543(6)A, α = 76.688(6), β = 72.299(6), γ = 88.157(6)°, V = 659.2(6) A^3, Z = 2, Mr = 274.39, Dc = 1.382 g/cm^3, μ = 0.386 mm^-1, F(000) = 288, R = 0.0586 and w R = 0.1808 for 2984 unique reflections with 2213 observed ones(I 〉 2σ(I)). The title compound was also screened for its antibacterial activities against Bacillus subtilis and Escherichia coli. The result indicates that the target compound presents potential antimicrobial activities, and that the minimum inhibitory concentration(MIC) values of the title compound against the two tested strains are both 62.5 μg/mL.
文摘A new kind of Schiff base HL(HL= 1-phenyl-3-methyl-4-(p-methylbenzoyl)-5-pyrazolone with L-Leucine methyl ester) and complexes Ni L′_2·0.75C_2H_5OH·0.25H_2O,Cu L′′2(L′ = 1-phenyl-3-methyl-4-(p-methylbenzoyl)-5-pyrazolone with L-leucine ethyl,L′′ = 1-phenyl-3-methyl-4-(p-methylbenzoyl)-5-pyrazolone with L-leucine) have been synthesized and structurally determined by X-ray diffraction. For HL: crystal structure determination indicates that there are two independent HLs with different conformations in one asymmetric unit. For complex 1: the Ni(Ⅱ) ion is six-coordinated by two carbonyl oxygen atoms from pyrazolone ring,two nitrogen atoms from different HL′ and two oxygen atoms from L-Leucine ethyl ester to form a distorted octahedral geometry. For complex 2: the Cu(Ⅱ) ion is four-coordinated by one carbonyl oxygen atom from the pyrazolone ring,one nitrogen atom from HL′′,and two different carboxylic oxygen atoms from L-leucine with the same conformation to form a distorted quadrilateral geometry.
文摘Nine novel erythromycin O-alkylamidoxime derivatives were prepared in excellent yields via the condensation of different O-alkylhydroxylamines with erythromycin imino ether. The structures of all the compounds prepared were confirmed by ^1 H NMR, 13C NMR, IR and MS, and their in vtiro antibacterial activities were tested. Among the compounds, two of them showed good antibacterial aetivities.
基金This work was supported by the Natural Science Foundation of Zhejiang Province (No. M203115) and Scientific Research Fund of Zhejiang Provincial Education Department (No. 20050057, 20050051)
文摘The title compound C18H22N4O4 was synthesized by the reaction of 3-hydrazine-4-hydroxy-6-methyl-2(1H)-pyridinones with 2-hydroxy-4-diethylaminobenzaldehyde in ethanol and characteri- zed by IR, tH NMR and elemental analysis. The single-crystal structure has been determined by X-ray diffraction analysis. The crystal belongs to the triclinic system, space group P1^- with a = 10.1930(14), b = 12.5200(17), c = 15.1863(19) A, α= 96.292(3), β= 96.450(3), γ= 102.443(3)°, V= 1862.6(4) A^3, Z= 4, Mr = 358.40, μ = 0.092 mm^-1, D c= 1.278 g/cm^3, F(000) = 760 and R = 0.0803. The crystal structure involves intermolcular N-H…O as well as intramolcular O-H…N, O-H…O and N-H…O hydrogen bonds. The title compound shows no antibacterial activity.
基金supported by the China Postdoctoral Science Foundation (No.20110491380)the Fundamental Research Funds for the Central Universities (No.ZYGX2009J085)
文摘Two Schiff base complexes [Cu(L)2] (1) and [Zn(L)2]·3H2O(2) of (E)-4-fluoro-2-((3-morpholino propylimino)methyl)phenol (HL) have been synthesized and characterized by elemental analysis and single-crystal X-ray diffraction. Crystal data for 1: triclinic, space group Pī with a=4.8000(10), b=11.109(2), c=13.921(3),α=66.55(3),β=80.35(3),γ=81.09(3)°, V=668.2(2)3 , Z=1, Dc=1.477g/cm 3 , F(000)=311, and the final R=0.0744 and wR=0.1601 for 2301 observed reflections with I 〉 2σ(I). And those for 2: monoclinic, space group P21 /c with a=14.789(3), b=11.713(2), c=18.846(4),β=107.85(3)°, V=3107.4(11)3 , Z=4, D c=1.389 g/cm 3 , F(000)=1368, and the final R=0.0749 and wR=0.1348 for 5423 observed reflections with I 〉 2σ(I). Both 1 and 2 are four-coordinated complexes, with a square-planar geometry of copper(Ⅱ) in 1 and a slightly distorted tetrahedral geometry of zinc(Ⅱ) in 2. An asymmetric unit consists of only one half of a Cu ion and one L ligand in 1, while an asymmetric unit is composed of one Zn ion, two L ligands and three water molecules in 2. Non-classical C-H···O and C-H F hydrogen bonds play important roles in the formation of a 1D chain of 1, but O-H O and O-H N hydrogen bonds play dominant roles in the self-assembly of a 3D network of 2. The antibacterial activities of 1 and 2 against B. subtilis, S. aureus, S. faecalis, P. aeruginosa, E. coli and E. cloacae have been evaluated by MTT method.
基金This work was supported by the Natural Science Foundation of Zhejiang Province (No. M203115) and Scientific Research Fund of Zhejiang Provincial Education Department (No. 20050057)
文摘The title compound C18H18N4OS has been synthesized by the reaction of 3-(2-hydroxy- benzyl)-4-amino-(1H)-1,2,4-triazole-5-thione with 4-isopropylbenzaldehyde in ethanol and characterized by IR, ^1H NMR spectra and elemental analysis. Its structure was determined by X-ray diffraction analysis. The crystal belongs to monoclinic, space group P21/c with a = 11.605(2), b = 7.401(1), c = 20.339(2) A, β= 103.05(2)°, V= 1701.8(4) A^3, Z = 4, Mr = 338.42,μ = 0.202 mm^-1, Dc = 1.321 g/cm^3 and F(000) = 712. The structure was solved by direct methods and refined to R = 0.0428 and wR = 0.1069. Due to the intramolecular O-H…N hydrogen bond and π-π stacking interactions between the benzene (C(1)~C(6)) and triazole rings, the two planes are essentially coplanar. Their biological activities have been measured, showing this type of compound has certain antibacterial activity for Staphylococous aureus and Bacillus subtilis. Based on the quantum chemistry calculation at the RHF/6-31G level, the frontier orbitals and electrostatic potential of the title compound were also discussed.
基金Supported by the Natural Science Foundation of Zhejiang Province (No. Y406049)Scientific Research Fund of Zhejiang Provincial Education Department (No. 20060079)
文摘In the ethanol solvent, a nickel(Ⅱ) complex Ni(C12H10N2O2S)2 upon reaction of 2'-(2-thienylidene)-hydroxybenzoylhydrazide with nickel acetate was synthesized, and its structure was characterized by IR, UV, elemental analysis and X-ray diffraction analysis. The crystal belongs to monoclinic system, space group C2/c with a = 22.052(3), b = 5.9681(6), c = 18.522(2)A , β = 110.679(4)°, V = 2280.6(4)A^3, Z = 4, Mr = 551.27, μ = 1.606 mm^-1, Dc = 1.075 g/cm^3, F(000) = 1136 and Rint = 0.0556. The nickel(Ⅱ ) atom in the compound is four-coordinated with two nitrogen atoms from amide and two oxygen atoms from keto group. The biological activities have been measured, show- ing the compound exhibits better anti-bacterial activity than the ligand.
文摘The chemical study of <i>Rumex</i> <i>abyssinicus</i> Jacp (Polygonaceae) led to the iso<span>lation of a new ceramide named</span> (<i>R</i>)-2</span><span style="font-family:"">'</span><span style="font-family:"">-hydroxy-<i>N</i>-[(2<i>S</i>,3<i>S</i>,4<i>R</i>,16<i>E</i>)-1,3,4-trihy<span>droxyhexacos-16-en-2-yl]hexadecanamide (rumexamide) (<b>1</b>) together with</span> sixteen known compounds: bis-(2-ethylhexyl) phthalate (<b>2</b>), chrysophanol (<b>3</b>), physcion (<b>4</b>), citreorosein (<b>5</b>), emodin (<b>6</b>), chrysophanein (<b>7</b>), physcionin (<b>8</b>), <span>lupeol (<b>9</b>), 3<i>β</i>,28-dihydroxylup-20(29)-ene (<b>10</b>), 3<i>β</i>-dihydroxylup-</span>20(29)-en-28-oic acid (<b>11</b>), oleanolic acid (<b>12</b>), ergosta-6,22-diene-3,5,8-triol (<b>13</b>), stigmastane-3,6-dione (<b>14</b>), a mixture of <i>β</i>-sitosterol (<b>15</b>) and stigmasterol (<b>16</b>), and <span>stigmasterol 3-<i>O</i>-<i>β</i>-<i>D</i>-glucoside (<b>17</b>). Their structures were determined by </span>in<span>terpretation of their spectroscopic 1D NMR (<sup>1</sup>H and <sup>13</sup>C NMR), 2D NMR</span> (COSY <sup>1</sup>H-<sup>1</sup>H, HSQC and HMBC) data in conjunction with mass spectrometry<span> </span>(TOFESIMS and HR-TOFESIMS) and by comparison with those reported in the literature. Among all the known compounds, twelve <b>(2</b>, <b>5</b>, <b>8</b></span><b><span style="font-family:"">-</span></b><b><span style="font-family:"">17) </span></b><span style="font-family:"">were firstly isolated from <i>Rumex</i> <i>abyssinicus</i>, seven <b>(2, 10</b></span><b><span style="font-family:"">-</span></b><b><span style="font-family:"">14 and 17)</span></b><span style="font-family:""> from the genus <i>Rumex</i> and three (<b>13, 14, 17</b>) from family Polygonaceae. The <i>in</i> <i>vitro</i> antibacterial activities of extracts (MeOH, <i>n</i>-BuOH and EtOAc)</span><span style="font-family:"">,</span><span style="font-family:""> as well as compounds <b>9</b>, <b>11, 12</b>, <b>15</b></span><b><span style="font-family:""> </span></b><b><span style="font-family:"">+</span></b><b><span style="font-family:""> </span></b><b><span style="font-family:"">16</span></b><span style="font-family:""> and <b>17 </b>against pathogenic bacteria (<i>Staphylococcus</i> <i>aureus</i> ATCC 43300, <i>Shigella</i> <i>flexneri</i> NR 518, <i>Klebsiella</i> <i>pneumonia</i></span><i><span style="font-family:"">e</span></i><span style="font-family:""> ATCC 700603, <i>Escherichia</i> <i>coli</i> ATCC 25922)</span><span style="font-family:"">,</span><span style="font-family:""> were performed using </span><span style="font-family:"">the </span><span style="font-family:"">broth microdilution method and the results show that, extract</span><span style="font-family:"">s</span><span style="font-family:""> were not active (MIC </span><span style="font-family:"">></span><span style="font-family:""> </span><span style="font-family:"">1000 μg/mL) while compounds were weakly or not active (MIC ≥ 500 μg/mL) against all bacteria strains. Furthermore, the chemophenetic relationship</span><span style="font-family:"">s</span><span style="font-family:""> of the isolated compounds and their significance</span><span style="font-family:"">s</span><span style="font-family:""> were discussed.
文摘A complex [NIL2] was synthesized, in which L, or to be exact, a Schiff base ligand (HL), was derived from the condensation of 1-phenyl-3-methyl-4-phenylacetyl-5-pyrazolone (PMPAP) with L-phenylalanine methyl ester. They were characterized by IR and single-crystal X-ray diffraction. Green block crystals of both ligand and its complex were grown at room temperature. The ligand, which consists of two individual fragments, crystalizes in the P1 space group (a = 5.6268(5), b = 10.6892(11) and c = 19.4869(18) A). The complex crystalizes in the P21 space group (a -- 21.4076(18), b = 9.4792(8) and c = 25.287(2) A), which consists of a nickel six-coordinated compound. Every fragment is a distorted octahedron with four oxygen and two nitrogen atoms. The Schiff base ligand (HL) and its complex have been tested in vitro to evaluate their antibacterial activity against bacteria Escherichia Coli and Bacillus subtilis. It is found that the complex has higher activity than the corresponding free Schiff base ligand (HL) against the same bacterial.
基金Supported by Hubei Province Natural Science Fund( 99J0 5 6 )
文摘A series of Benzisolselenazolone (BISA) derivatives were synthesized and evaluated for their antibacterial activities againstE coli. by using LKB-2277 bioactivity monitor. Other bioactivities were tested by the method of High Throughput Screening for pharmaceutical activity compounds (HTP) BISA derivatives 3b, at the concentration of 40 μg/mL, showed 100%antibacterial activity and 62%inhibition rate of aldose reductase (at the concentration of 5μg/mL). These new compound structures have determined by IR,1H NMR and MS spectra.