9 results about "Nitrofuran" patented technology

The present application relates to the technical field of nitrofurans metabolite content determination, and particularly relates to a method for determining the residual amount of nitrofurans metabolite in propolis. The method is that the pretreated propolis sample is detected by liquid chromatography-tandem mass spectrometry after gradient elution of the mobile phase; the pretreatment is that the propolis sample is sequentially hydrolyzed by hydrochloric acid, purified by HLB solid phase extraction column, derivatized by o-nitrobenzaldehyde, and purified by ethyl acetate treatment. The present application purifies the propolis sample after hydrochloric acid hydrolysis before o-nitrobenzaldehyde derivatization, so that o-nitrobenzaldehyde fully reacts with the nitrofurans metabolite in propolis, and the residual amount of nitrofurans metabolite in propolis is accurately detected by combining the selection and gradient elution of the mobile phase.

Novel compounds and methods of killing or inhibiting the growth of bacteria.

The present application relates to a kind of construction method of electrochemical sensor based on nitrogen-doped carbon cobalt nickel diatomic catalyst and its application, the electrochemical sensor is the composite material after nitrogen-doped carbon cobalt nickel diatomic catalyst is mixed with film-forming material is made on the surface of glassy carbon electrode and is prepared.The electrochemical sensor provided by the present application has high stability and selectivity, double metal center synergistic effect, shows excellent catalytic performance, significantly improves electrochemical reaction activity, and improves the sensitivity of sensor.The electrochemical sensor is used to detect carbazochrome, and has high detection sensitivity and response speed, especially in trace detection and complex sample anti-interference aspect has advantage.The present application can be applied to food safety monitoring, such as rapid detection of carbazochrome residue in animal feed or meat, and can also be used for trace detection of nitrofurans in water or soil, and has wide application prospect.

The application discloses a kind of detection methods of nitrofurans metabolites in macrobrachium rosenbergii based on UPLC-MS / MS and application thereof, belong to aquatic product safety evaluation detection technical field.The application utilizes QuECHERS method to the pretreatment of macrobrachium rosenbergii sample, extracts nitrofurans metabolites, including adding acidified acetonitrile extraction, adding ammonium acetate, water removal and adding dispersed solid extraction column to reduce matrix effect and other steps.After the QuECHERS method of the application is handled, the obtained nitrofurans metabolites do not need to be subjected to derivatization procedure, can directly use HILIC hydrophilic chromatographic column, in positive ion mode liquid chromatography-mass spectrometry analysis, detect aminourea and other nitrofurans metabolites.The detection method provided by the application has the advantages of high sensitivity, strong accuracy, wide applicability, compared with traditional detection method, can avoid reagent waste, save a lot of time.

The application provides a Cd(II) coordination polymer, the chemical expression of the polymer is {[Cd2(bptc)(dpb) 1.5 (H2O)]·(H2O)·0.5(dpb)} n , wherein H4bptc is 2,3,3',4'-biphenyl tetracarboxylic acid organic ligand, dpb is 1,4-di(pyridin-4-yl)benzene (dpb) nitrogen-containing ligand, the crystal of the complex belongs to a triclinic system, the space group is Pī, the cell parameters are c=13.3406(3), α=110.165(1)°, β=107.476(1)°, γ=97.459(1)°, and the asymmetric unit is composed of 2 crystallographically independent Cd 2+ ions (Cd1, Cd2), 1 deprotonated bptc 4‑ ligand, 3 dpb ligands (dpbI, dpbII, dpbIII; occupancy: dpbI is 1, and dpbII and dpbIII are 0.5), 1 coordinated water molecule (O9) and 1 lattice water (O10). The Cd(II) coordination polymer provided by the application can be used for specific detection of nitrofuran antibiotics in irrigated water bodies.

The application provides a high-sensitivity detection method for multi-residues of veterinary drugs in pig urine, and belongs to the technical field of detection of veterinary drug residues. The application first performs enzymatic treatment on the sample to be detected, thereby improving the detection sensitivity of salbutamol and ractopamine; then performs acid hydrolysis and derivatization treatment on the sample to be detected, thereby improving the reversed-phase chromatographic retention performance and mass spectrometry ionization efficiency of nitrofurans in the compound to be detected, improving the sensitivity, improving the polarity of the compound to be detected, thereby improving the chromatographic separation effect, effectively separating the interfering substances in the matrix, improving the anti-interference ability of the detected substance, and indirectly improving the detection sensitivity; clenbuterol, metronidazole, dimetridazole, olaquindox, chlorpromazine and chloramphenicol are mainly in free state, and are not affected by enzymatic and acid hydrolysis and derivatization during detection, can be detected together with the above-mentioned compounds to be detected, and the mass spectrometry derivatization and sensitivity detection of multi-residues of cross-class veterinary drugs are realized.

The invention provides a nitrofuran metabolite magnetic surface molecularly imprinted polymer as well as a preparation method and application thereof, and relates to the technical field of molecularly imprinted polymers. The preparation method comprises the following steps: by virtue of a surface imprinting polymerization method, taking CS-Fe3O4-coated HNTs as a carrier, and taking AHD and AMOZ as dual-template molecules; mAA is a functional monomer; a deep eutectic solvent synthesized by choline chloride and p-coumaric acid is used as an auxiliary functional monomer, AIBN is used as an initiator, and EGDMA is used as a cross-linking agent; the magnetic surface molecularly imprinted polymer is prepared by using a magnetic solid-phase extraction technology as a template and acetonitrile as a pore-foaming agent, and is successfully applied to enrichment and detection of nitrofuran metabolites in an actual sample by combining a magnetic solid-phase extraction technology and high performance liquid chromatography. According to the method, trace detection of nitrofuran metabolites such as AOZ, AMOZ, AHD and SEM can be achieved, the detection limit is as low as 0.25-0.93 ng / mL, and the adding standard recovery rate is 80-95% RSDlt; 3.5%; the zebra fish can also be applied to water environment restoration, the survival rate of zebra fish is remarkably increased, and it is proved that the zebra fish has toxicology relieving and ecological restoration functions.

The application discloses a furan oxadiazole ketone compound and a preparation method and application thereof in detecting CO3 2‑ or PO4 3‑ . The furan oxadiazole ketone compound has a structural formula. The application further provides a preparation method of the furan oxadiazole ketone compound, which comprises the following steps: reacting 5-nitrofuran-2-carboxylic acid and oxalyl chloride to obtain 5-nitrofuran-2-carbonyl chloride, then acylating 2-hydrazinyl pyrimidine with 5-nitrofuran-2-carbonyl chloride to obtain 5-nitro-N'-(2-pyrimidinyl) furan-2-carbonyl hydrazine, and forming a ring of the 5-nitro-N'-(2-pyrimidinyl) furan-2-carbonyl hydrazine with triphosgene to obtain the furan oxadiazole ketone compound. The furan oxadiazole ketone compound provided by the application is an optical probe, which can be used as a fluorescent probe to detect CO3 2‑ or PO4 3‑ in environmental water bodies, and has strong anti-interference ability.

The invention discloses a 4-(2-(methylamino) thiazole-5-yl) pyrimidine-2-amine derivative and application thereof, the structural formula of the 4-(2-(methylamino) thiazole-5-yl) pyrimidine-2-amine derivative is shown in the specification, in the formula, R1 is hydrogen or methyl; r2 is a substituted benzoyl group, a substituted phenylacetyl group, and a substituted or unsubstituted benzene propionyl group; and R3 is a substituted phenyl group, a 5-nitrofuran-2-yl group or a 1H-imidazole-2-yl group. As a novel CDK9 inhibitor, the ESCC inhibitor fills the blank of special medicines for ESCC; pharmaceutical salts and compositions can be prepared, and development of oral or injection preparations is facilitated; the compound is suitable for esophageal cancer single-drug treatment or is combined with other targeting / immune / chemotherapeutic drugs to improve the curative effect and reduce the drug resistance risk; meanwhile, other CDK9 related tumors such as lung cancer and breast cancer can be expanded.