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34 results about "Antituberculous drug" patented technology

Chirality 7-(piperazine-substituted pyrazol aldehyde condensation isoniazide) fluoroquinolone carboxylic acid derivative as well as preparation method and application thereof

The invention discloses a chirality 7-(piperazine-substituted pyrazol aldehyde condensation isoniazide) fluoroquinolone carboxylic acid derivative as well as a preparation method and application thereof. The chirality 7-(piperazine-substituted pyrazol aldehyde condensation isoniazide) fluoroquinolone carboxylic acid derivative is a compound with the general structural formula (I), wherein R1 is H, methyl or ethyl, and R2 is H or methyl. According to the chirality 7-(piperazine-substituted pyrazol aldehyde condensation isoniazide) fluoroquinolone carboxylic acid derivative provided by the invention, fluoroquinolone, isoniazide and pyrazole aldehyde hydrazone are effectively combined to form a compound with a new structure; superposition and cooperation of activity are achieved; superposition of the three pharmacophores of fluoroquinolone, isoniazide and pyrazole aldehyde hydrazone is realized, the antituberculosis activity is improved, the toxic and side effects of fluoroquinolone and isoniazide to normal cells are decreased, and meanwhile, the probability that mycobacterium tuberculosis resists such drugs can be lowered; the chirality 7-(piperazine-substituted pyrazol aldehyde condensation isoniazide) fluoroquinolone carboxylic acid derivative can serve as an antituberculous active substance used for development of an antituberculous drug with a new structure.
Owner:HENAN UNIVERSITY +1

Substituted 1,3-miscellaneous azole compound, preparation method thereof, pharmaceutical composition containing substituted 1,3-miscellaneous azole compound and purpose thereof

The invention relates to a substituted 1,3-miscellaneous azole compound, a preparation method thereof, a pharmaceutical composition containing the substituted 1,3-miscellaneous azole compound and a purpose thereof. The invention relates to the compound in a formula I, or its pharmaceutically acceptable salt, a stereisomer or a solvate, wherein R1, R2, R3 and X are defined as a specification; and the invention also relates to the preparation method, the pharmaceutical composition containing the substituted 1,3-miscellaneous azole compound and the purpose thereof. The compound of the present invention is the novel antituberculous compound, is effective to mycobacterium tuberculosis-susceptible strains, also possesses activity on strains with tolerance on traditional first-line antituberculous drugs such as isoniazide and rifampicin, and has good selectivity to mycobacterium tuberculosis.
Owner:MEDICINE & BIOENG INST OF CHINESE ACAD OF MEDICAL SCI

Triple compound microsphere vascular targeted embolization sustained-release preparation containing antituberculous drug as well as preparation method and application of preparation

ActiveCN104324032AExcellent anti-tuberculosis effect in vitro and in vivoReduce concentrationAntibacterial agentsOrganic active ingredientsAntituberculous drugHemoptyses
The invention relates to a triple compound microsphere vascular targeted embolization sustained-release preparation containing an antituberculous drug as well as a preparation method and application of the preparation. The sustained-release agent comprises a carrier and drugs, wherein the drugs are coated with the carrier; the carrier is sodium alginate or chitosan, and the drugs are triple antituberculous compound drugs including rifampicin, isoniazid and pyrazinamide or moxifloxacin. The three antituberculous drugs are matrix drug solutions, the sodium alginate or chitosan is a carrier solution, the matrix drug solutions and the carrier solutiona are mixed to prepare a solution, the polymer solution containing drugs is dispersed into fogdrops with a certain diameter by adopting a high-voltage electrostatic droplet mode, and the fogdrops are sprayed into a solidifying liquid to prepare antituberculous drug microspheres under the action of calcium ions. The embolization sustained-release preparation can be used for treating tuberculosis, massive hemoptysis of pulmonary tuberculosis, tuberculosis cavity, renal tuberculosis, osteoarticular tuberculosis, genital tuberculosis, tuberculosis of thyroid gland, tuberculosis of cervical lymph nodes, tuberculosis of pericardium, tuberculosis of chest wall, pleural tuberculosis and other kinds of tuberculosis in a body.
Owner:THE 309TH HOSPITAL OF CHINESE PEOPLES LIBERATION ARMY +1

Antituberculous drug drug-resistance gene and screening method thereof

The invention discloses an antituberculous drug drug-resistance gene and a screening method thereof. The antituberculous drug drug-resistance gene is pks12, pks5, PPE34, Rv1978, Rv1847, hemK, PPE3, glyA1, PE_PGRS27, PE_PGRS19, Rv1520, Rv1505c, Rv2407, mmuM, vapB17, Rv3727 and Rv3737. The novel candidate drug target gene is provided for a further understanding of drug resistance mechanism of MDR / XDR mycobacterium tuberculosis and the therapy of MDR / XDR-TB.
Owner:AFFILIATED HOSPITAL OF ZUNYI MEDICAL COLLEGE

Ubiquitin-interacting motif-like structural domain of mycobacterium tuberculosis secretory protein

The invention discloses an ubiquitin-interacting motif-like (UIML) structural domain of mycobacterium tuberculosis secretory protein, and belongs to the field of cytobiology. The ubiquitin-interacting motif-like structural domain of PtpA and a key binding site (A140) thereof are determined for the first time; the ubiquitin-interacting motif-like structural domain comprises the 115th amino acid of PtpA protein to the 161th amino acid of the PtpA protein, wherein hydrophobic interaction of hydrophobic amino acid sequence EEVFAVIESA (136-145) with ubiquitin (Ub) can be realized; and mutation of the A140 site of the UIML structural domain is capable of resulting in loss of binding capacity of Ub with PtpA, and loss of enzyme activity regulatory functions of Ub. The ubiquitin-interacting motif-like (UIML) structural domain is capable of providing specific sequences for screening of PtpA molecule-based antituberculous drugs and vaccine development, providing treatment of a plurality of diseases in clinic with novel tools and ideas, possesses promising prospect in development and clinical application of a plurality of drugs such as antitumor drugs, and can be directly used for scientific research field or for guiding development of preparations used for reversible control of JNK and P38 signal channels.
Owner:INST OF MICROBIOLOGY - CHINESE ACAD OF SCI

Kit and method for detecting antituberculous drugs and metabolites thereof in sample

PendingCN114354804AExpand the types of testingIncrease varietyComponent separationMetaboliteAntituberculous drug
The invention particularly provides a kit and a method for detecting antituberculous drugs and metabolites thereof in a sample. The kit is used for detecting antituberculous drugs and metabolites thereof in a sample, and comprises a calibration product, a quality control product, an instrument quality control product and an isotope internal standard product, both the calibration material and the quality control material contain rifampicin, isoniazide, rifapentine, pyrazinamide, ethambutol, clofazimine, cycloserine, moxifloxacin, levofloxacin, linezolid, acetyl isoniazide, bedaquiline and deacetylrifampicin; the instrument quality control product comprises a methanol solution containing rifampicin, isoniazid, rifapentine, pyrazinamide, ethambutol, clofazimine, cycloserine, moxifloxacin, levofloxacin, linezolid, acetyl isoniazid, bedaquiline and deacetylrifampicin; the isotope internal standard substance contains an internal standard substance corresponding to a substance contained in the calibrator. The kit disclosed by the invention can be used for detecting the concentrations of the antituberculous drugs and metabolites thereof in various sample types.
Owner:THE THIRD PEOPLES HOSPITAL OF SHENZHEN

Mycobacterium tuberculosis antigen protein Rv1798 and application of T cell epitope peptide of Mycobacterium tuberculosis antigen protein Rv1798

The invention relates to mycobacterium tuberculosis antigen protein Rv1798 and application of a T cell epitope peptide of the mycobacterium tuberculosis antigen protein Rv1798 in preparation of tuberculosis detection reagents, vaccines and drugs. An amino acid sequence of the mycobacterium tuberculosis protein antigen Rv1798 and an amino acid sequence of the T cell epitope peptide of the protein antigen Rv1798 are shown in SEQ ID NO:1-3 respectively. The mycobacterium tuberculosis protein antigen Rv1798 and the T cell epitope peptide thereof are applied to a specific T cell and B cell immune response caused by mycobacterium tuberculosis by serving as irritants; and when the mycobacterium tuberculosis protein antigen Rv1798 and the T cell epitope peptide thereof are applied to the specific T cell and B cell immune response caused by the mycobacterium tuberculosis by serving as the irritants, the condition that a false positive result is caused due the fact that an antigen is not pure can be reduced compared with an original method that a complete antigen is adopted. The detection reagents prepared from the protein antigen Rv1798 and the epitope peptide thereof can be widely applied to the related fields of assistant diagnosis of tuberculosis, epidemiological monitoring and the like. The tuberculosis vaccines and the antituberculous drugs which are prepared from the protein antigen Rv1798 can be used for preventing and treating the tuberculosis.
Owner:ICDC CHINA CDC +1

Near-infrared cyanine colorimetric fluorescent probe and preparation method and application thereof

The invention discloses a near-infrared cyanine colorimetric fluorescent probe and a preparation method and application thereof. The structural formula of the probe is shown as a formula (I). The fluorescent probe can identify and detect N2H4 in a mixed solution of absolute ethyl alcohol and a PBS by utilizing fluorescence and an ultraviolet-visible absorption spectrum. The probe has high selectivity and sensitivity in N2H4 identification, strong anti-interference capability and very low detection limit; the fluorescent probe can be applied to detection of environmental pollution or in-vitro and in-vivo antituberculous drug metabolites N2H4.
Owner:SHENZHEN INST OF ADVANCED TECH CHINESE ACAD OF SCI

Primer, probe and kit for detecting gene mutation sites related to drug resistance of mycobacterium tuberculosis and treatment drugs

The invention relates to the technical field of medical detection, in particular to a primer, a probe and a kit for detecting mycobacterium tuberculosis and drug-resistant gene mutation sites. The detection primer and the probe comprise DNA (deoxyribonucleic acid) sequences as shown in SEQ ID NO: 1 to SEQ ID NO: 68. The drug resistance type of mycobacterium tuberculosis is detected based on a Luminex liquid chip, whether the mycobacterium tuberculosis exists in a sample or not can be detected, four first-line antituberculous drugs including isoniazide, rifampicin, pyrazinamide and streptomycin and a second-line antituberculous drug, namely fluoroquinolone, are covered, mutation sites are comprehensive, the detection speed is high, only 3.5 hours are needed to complete one-time detection, and as many as 96 samples can be detected at the same time at one time. Therefore, the detection process is simplified, the experimental period is shortened, the detection accuracy and sensitivity are improved, and clinical application is facilitated.
Owner:HAINAN MEDICAL COLLEGE

LC-MS/MS method for quantitatively analyzing plasma concentration of antituberculous drug

PendingCN112924613ASolving problems with large polarity differencesEasy to handleComponent separationAntituberculous drugPyrazine
The invention discloses an LC-MS / MS method for quantitatively analyzing the plasma concentration of an antituberculous drug. The method can simultaneously detect isoniazide, rifampicin, pyrazinamide and ethambutol through S1 standard working solution preparation, S2 sample preparation, S3 sample treatment, S4 sample detection and S5 standard curve making and quantitative analysis, the sample pretreatment process is simple and is easy to operate, and all the reagents are conventional reagents, so that the cost is lower. According to the method, a reversed-phase C18 column of 150 mm*2.1 mm is adopted, the flow rate is controlled to be 0.3 mL / min, and the column temperature is 30 DEG C; the problem that the polarity difference of isoniazide, rifampicin, pyrazinamide and ethambutol is large can be well solved, the separation effect is better, and the cost is lower. The method has the advantages of higher sensitivity, accuracy and precision, wide detection linear range and short detection time, and can be used as a reliable detection method suitable for popularization and for monitoring the treatment concentration of clinical first-line anti-tuberculosis drugs.
Owner:XIANGYA HOSPITAL CENT SOUTH UNIV

Derivative of 7-(piperazine substituted pyrazole aldehyde isoniazid hydrazone) fluoronaphthyridinone carboxylic acid as well as preparation method and application of derivative

The invention discloses a derivative of 7-(piperazine substituted pyrazole aldehyde isoniazid hydrazone) fluoronaphthyridinone carboxylic acid as well as a preparation method and an application of the derivative. The derivative of the 7-(piperazine substituted pyrazole aldehyde isoniazid hydrazone) fluoronaphthyridinone carboxylic acid is a compound having a structural general formula (I), wherein R1 is H, methyl or ethyl; R2 is H or methyl. According to the derivative of the 7-(piperazine substituted pyrazole aldehyde isoniazid hydrazone) fluoronaphthyridinone carboxylic acid, fluoroquinolone, isoniazid and pyrazole aldehyde hydrazine are effectively combined to form a compound having a new structure, the joint of pharmacophores and the mutual complementation of structures are realized and the overlapping and cooperation of the activity are achieved; the antituberculous activity is added, the toxic and side effects of fluoroquinolone and isoniazid on normal cells are reduced, and meanwhile, the probability of drug resistance of mycobacterium tuberculosis to the drug is also reduced; as a result, the derivative can be used as an antituberculous active substance to develop antituberculous drug having a brand new structure.
Owner:HENAN UNIVERSITY

Application of polymorphism of retinoid X receptor alpha (RXRA) genes to adverse reactions of antituberculous drugs

The invention discloses application of polymorphism of retinoid X receptor alpha (RXRA) genes to adverse reactions of antituberculous drugs, and relates to the field of screening of adverse reactionsof tuberculous drugs. The invention discloses application of the polymorphism of the RXRA genes to tuberculosis treatment, it is found that through detection of the polymorphism of the RXRA genes, therisk of generating the adverse reactions after tuberculous patients are treated by the antituberculous drugs can be predicted, certain support is provided for avoiding the adverse reactions caused bythe related antituberculous drugs, and certain guidance is also provided for drug use of the tuberculous patients.
Owner:WEST CHINA HOSPITAL SICHUAN UNIV

Application of L-alanine in preparation of medicine for preventing and treating tuberculosis

The invention discloses application of L-alanine in preparation of a medicine for preventing and treating tuberculosis. By means of a C57BL / 6 mouse and SCID mouse infection model, a macrophage in-vitro infection model, an exogenous metabolite adding mode and the like, it is proved that L-alanine resists tubercle bacillus infection through natural immune cell protection host, L-alanine promotes macrophage antibacterial peptide generation and limits tubercle bacillus intracellular survival; and the L-alanine is expected to assist the current antituberculous drugs, can shorten the course of treatment and improve the curative effect, and provides reference for clinical treatment.
Owner:SHANGHAI PULMONARY HOSPITAL

Preparation method and application of antituberculous drug Pretomanid

The invention relates to a preparation method of an antituberculous drug Pretomanid and an application of the antituberculous drug Pretomanid. According to the preparation method, 2, 5-dibromo-4-nitroimidazole is taken as an initial raw material, and a nucleophilic substitution reaction, a reduction elimination reaction, an oxidation cyclization reaction, an epoxy ring-opening reaction, a nucleophilic substitution reaction, a deprotection reaction and a cyclization reaction are sequentially carried out to prepare the target product, namely the antituberculous drug Pretomanid. The raw materials used in the whole process are cheap and easy to obtain, explosive dinitroimidazole is prevented from being used, generation of 4-nitro isomers is avoided, and the method is simple in process operation, easy to control and convenient to purify and can be used for industrial production.
Owner:SHENYANG HONGQI PHARMA

Method for simultaneously determining eight antituberculous drugs in human plasma based on LC-MS

The invention belongs to the technical field of analytical chemistry, and particularly relates to a method for simultaneously determining the concentrations of eight antituberculous drugs in plasma by adopting a liquid chromatography-mass spectrometry method, wherein the eight antituberculous drugs comprise rifudine, chlorphenazine, levofloxacin, clarithromycin, sulfimide, p-aminosalicylic acid, moxifloxacin and amikacin. According to the method, the characteristics of hydrophilic and hydrophobic compounds are considered, protein precipitation is carried out by utilizing ACN:MEOH:45%TCA, the extraction rate of the hydrophilic compound AMK is improved, 20% of ACN, 0.2% of FA and 1% of HFBA are used as diluents, and the retention time of the hydrophilic compound AMK is prolonged by adding the HFBA. The method is high in sensitivity, strong in specificity and wide in linear range, can be used for qualitative and quantitative analysis of to-be-detected substances with unknown concentrations in plasma of tuberculosis patients, is simple and rapid to operate, does not need an extraction and volatilization process, and can meet the characteristics of urgent clinical treatment drug monitoring tasks and high requirements on detection time. The detection system provided by the invention provides a new technical platform for tuberculosis patient treatment drug monitoring, and is easy to popularize and apply.
Owner:SHANGHAI PUBLIC HEALTH CLINICAL CENT

High-throughput detection method of genotypic drug-resistant locus of mycobacterium tuberculosis

The invention discloses a high-throughput detection method of a genotypic drug-resistant locus of mycobacterium tuberculosis. In the method, the drug-resistant locus of an antituberculous drug of themycobacterium tuberculosis can be detected more comprehensively, more effectively and more quickly by utilizing a mutation database of used drug-resistant mycobacterium tuberculosis and combining a second generation high-throughput sequencing technology. According to the method, the difficulty that a false positive result is obtained as the silent mutation of important genes cannot be distinguished due to the limit to the number of detection gene loca in other detection methods of the drug-resistant locus is overcome; under the help of a high-throughput detection technology, more comprehensivediagnosis information can be provided for treating the drug-resistant mycobacterium tuberculosis better, so that the curative effect is improved, and the use of low-efficiency drugs is reduced.
Owner:JIAXING YUNYING MEDICAL INSPECTION CO LTD

Exosome compound with tumor inhibition effect

The invention discloses an exosome compound with a tumor inhibition effect. The exosome compound comprises exosomes of human mesenchymal stem cells and rifampicin. According to the invention, an exosome drug loading technology is utilized to load an antituberculous drug rifampicin into the human-derived mesenchymal stem cell exosome, and experiments find that the human-derived mesenchymal stem cell exosome has remarkable curative effects of inhibiting growth, proliferation, migration and invasion of tumors, can promote apoptosis and cell cycle arrest of the tumors, and can be used for preparing a medicine for treating the tumors. Particularly, the compound has an obvious growth inhibition effect on osteosarcoma cells. After being prepared into the tumor treatment medicine, the compound has important significance on improving the treatment effect of osteosarcoma patients, improving prognosis and increasing the survival rate.
Owner:厦门大学附属翔安医院 +1

7-(piperazine substituted pyrazole aldehyde isoniazid hydrazone)flunalidone carboxylic acid derivative and its preparation method and application

The invention discloses a derivative of 7-(piperazine substituted pyrazole aldehyde isoniazid hydrazone) fluoronaphthyridinone carboxylic acid as well as a preparation method and an application of the derivative. The derivative of the 7-(piperazine substituted pyrazole aldehyde isoniazid hydrazone) fluoronaphthyridinone carboxylic acid is a compound having a structural general formula (I), wherein R1 is H, methyl or ethyl; R2 is H or methyl. According to the derivative of the 7-(piperazine substituted pyrazole aldehyde isoniazid hydrazone) fluoronaphthyridinone carboxylic acid, fluoroquinolone, isoniazid and pyrazole aldehyde hydrazine are effectively combined to form a compound having a new structure, the joint of pharmacophores and the mutual complementation of structures are realized and the overlapping and cooperation of the activity are achieved; the antituberculous activity is added, the toxic and side effects of fluoroquinolone and isoniazid on normal cells are reduced, and meanwhile, the probability of drug resistance of mycobacterium tuberculosis to the drug is also reduced; as a result, the derivative can be used as an antituberculous active substance to develop antituberculous drug having a brand new structure.
Owner:HENAN UNIVERSITY

Isorcryptolepine analogue prepared by taking ofloxacin as raw material, and preparation method and application thereof

The invention discloses an isocryptolepine analogue, and a preparation method and application thereof. The chemical structure of the isocryptolepine analogue is shown as a formula I. The substituent group R in the formula I can be independently -H, -OCH3, -F, -Cl or -SO2NH2. According to the isocryptolepine analogue disclosed by the invention, ofloxacin is taken as a raw material, so that effective chemical construction from a fluoroquinolone structure to an indoloquinoline skeleton is realized, and a new way for structural modification of isocryptolepine is expanded, so that the anti-tubercle bacillus activity and the anti-drug resistance of the compound are improved, the toxicity to normal cells is reduced, and the isocryptolepine analogue can be further developed as an antituberculous drug with a brand new structure.
Owner:ZHENGZHOU UNIV OF IND TECH

Gene detection reagent for predicting liver injury caused by antituberculous drug, test kit and detection method

InactiveCN111979310APredict risk of adverse reactions to liver damageSolve the technical problem of risk prediction of adverse reactionsMicrobiological testing/measurementDNA/RNA fragmentationAntituberculous drugAntituberculous drugs
The invention provides a gene detection reagent for predicting liver injury caused by antituberculous drug, a test kit and a detection method, and relates to the technical field of tuberculosis treatment. The reagent is used for predicting the risk of adverse liver reaction caused by the antituberculous drug received by tuberculosis patients. The reagent comprises a genotype used for detecting anyone of the following SNPs sites of the LEPR gene: rs2025804 and rs2104564. According to the present invention, with the detection of the polymorphism of the LEPR gene, the risk of the adverse reaction after the tuberculosis patient receives the anti-tuberculosis drug treatment can be predicted, the certain support is provided for the prevention of the adverse reaction caused by the related anti-tuberculosis drug, and the certain guidance is provided for the medication of the tuberculosis patient.
Owner:WEST CHINA HOSPITAL SICHUAN UNIV

Antituberculous drug composition

InactiveCN106728305ADisappear whole bodyDisappear local symptomsAntibacterial agentsUnknown materialsMedicineAntituberculous drug
The invention discloses an antituberculous drug composition, prepared from the following components in parts by weight: 20 to 50 parts of Chinese honeylocust fruit, 10 to 30 parts of mineral Zilusha, 10 to 30 parts of flos sophorae, 5 to 10 parts of donkey-hide gelatin and 5 to 10 parts of rhizoma picrorhizae. The antituberculous drug composition has the advantages that growth of mycobacterium tuberculosis can be inhibited, the antibacterial activity is higher, and various tuberculosis diseases can be treated.
Owner:呼伦贝尔恒扬民间医药研究院

Application of Rv1773c in preparing drug for resisting infection of mycobacterium tuberculosis

The invention discloses application of Rv1773c in preparing a drug for resisting infection of mycobacterium tuberculosis and belongs to the technical field of biology. The invention determines that functional protein Rv1773c of the mycobacterium tuberculosis can promote the mycobacterium tuberculosis to intrude macrophage. The Rv1773c can be used as a novel drug target for resisting tuberculous infection. The results provided by the invention can provide a novel tool and an idea for preventing and treating clinical tuberculosis; particularly, the Rv1773c has a broad prospect in the aspects ofdevelopment, clinical application and the like of anti-tuberculosis drugs and vaccine, or can be directly applied to the field of scientific research or guides the development of an inhibitor for inhibiting the intrusion of the mycobacterium tuberculosis to host macrophages. The Rv1773c disclosed by the invention has important application value of obtaining a novel antituberculous drug target andscreening a novel drug.
Owner:WUHAN UNIV

Spine internal fixing device containing carrier for implanting antituberculous drugs into artificial bone in sustained-release mode

The invention discloses a spinal internal fixing device containing a carrier for implanting antituberculous drugs into an artificial bone in a sustained-release mode. The spinal internal fixing device containing the carrier for implanting the antituberculous drugs into the artificial bone in a sustained-release mode comprises fixing screws arranged at intervals and a connecting rod connecting the two fixing screws, wherein tuberculosis treatment drugs are arranged in the fixing screws and / or the connecting rod, the outer wall of each fixing screw and the outer wall of the connecting rod are provided with drug passing holes allowing the tuberculosis treatment drugs to be released, positioning devices used for fixing the tuberculosis treatment drugs are arranged in the fixing screws and the connecting rod, and the tuberculosis treatment drugs comprise a slow-release drug carrier, isoniazide, rifampicin and streptomycin.
Owner:SHANGHAI PULMONARY HOSPITAL

Chiral 7-(piperazine substituted pyrazole aldehyde isoniazid hydrazone) fluoroquinolone carboxylic acid derivative and its preparation method and application

The invention discloses a chirality 7-(piperazine-substituted pyrazol aldehyde condensation isoniazide) fluoroquinolone carboxylic acid derivative as well as a preparation method and application thereof. The chirality 7-(piperazine-substituted pyrazol aldehyde condensation isoniazide) fluoroquinolone carboxylic acid derivative is a compound with the general structural formula (I), wherein R1 is H, methyl or ethyl, and R2 is H or methyl. According to the chirality 7-(piperazine-substituted pyrazol aldehyde condensation isoniazide) fluoroquinolone carboxylic acid derivative provided by the invention, fluoroquinolone, isoniazide and pyrazole aldehyde hydrazone are effectively combined to form a compound with a new structure; superposition and cooperation of activity are achieved; superposition of the three pharmacophores of fluoroquinolone, isoniazide and pyrazole aldehyde hydrazone is realized, the antituberculosis activity is improved, the toxic and side effects of fluoroquinolone and isoniazide to normal cells are decreased, and meanwhile, the probability that mycobacterium tuberculosis resists such drugs can be lowered; the chirality 7-(piperazine-substituted pyrazol aldehyde condensation isoniazide) fluoroquinolone carboxylic acid derivative can serve as an antituberculous active substance used for development of an antituberculous drug with a new structure.
Owner:HENAN UNIVERSITY +1

Method for detecting residual quantity of antituberculous drugs in beef and mutton

The invention discloses a method for detecting the residual quantity of antituberculous drugs in beef and mutton, and relates to the technical field of beef and mutton detection. The method comprises the following steps of: S1, extracting beef and mutton tissue soaking liquid; according to the method for detecting the residual quantity of the antituberculous drugs in beef and mutton, dinitrophenylhydrazine and streptomycin react in an acid solution to generate yellow color, and the detected absorbance value is compared with an absorbance standard curve, so that the residual quantity of the antituberculous drugs is obtained. According to the method, the existence and size of an inhibition zone on a reagent plate containing bacillus subtilis liquid in a test box are observed, the residual quantity of the antituberculous drugs is obtained by contrasting an observation result with an inhibition zone standard curve, a standard numerical value is analyzed and obtained according to the two obtained numerical values, and if the difference between the two numerical values is large, an experiment is performed again, so that the accuracy of the detection method is improved, and deviation of a detection result caused by detection by using a single detection method is prevented, so that food safety is guaranteed.
Owner:XINJIANG ACADEMY OF ANIMAL SCI QUALITY STANDARDS INST OF ANIMAL HUSBANDRY XINJIANG UYGUR AUTONOMOUS REGION SHEEP & WOOL CASHMERE QUALITY SAFETY SUPERVISION & INSPECTION CENT

Application of Mycobacterium tuberculosis antigenic protein rv1798 and its T cell epitope peptide

The invention relates to mycobacterium tuberculosis antigen protein Rv1798 and application of a T cell epitope peptide of the mycobacterium tuberculosis antigen protein Rv1798 in preparation of tuberculosis detection reagents, vaccines and drugs. An amino acid sequence of the mycobacterium tuberculosis protein antigen Rv1798 and an amino acid sequence of the T cell epitope peptide of the protein antigen Rv1798 are shown in SEQ ID NO:1-3 respectively. The mycobacterium tuberculosis protein antigen Rv1798 and the T cell epitope peptide thereof are applied to a specific T cell and B cell immune response caused by mycobacterium tuberculosis by serving as irritants; and when the mycobacterium tuberculosis protein antigen Rv1798 and the T cell epitope peptide thereof are applied to the specific T cell and B cell immune response caused by the mycobacterium tuberculosis by serving as the irritants, the condition that a false positive result is caused due the fact that an antigen is not pure can be reduced compared with an original method that a complete antigen is adopted. The detection reagents prepared from the protein antigen Rv1798 and the epitope peptide thereof can be widely applied to the related fields of assistant diagnosis of tuberculosis, epidemiological monitoring and the like. The tuberculosis vaccines and the antituberculous drugs which are prepared from the protein antigen Rv1798 can be used for preventing and treating the tuberculosis.
Owner:ICDC CHINA CDC +1

Application of medicine nintedanib for resisting idiopathic pulmonary fibrosis in tuberculosis treatment

The invention relates to an application of nintedanib or a pharmaceutical salt thereof in preparation of a medicine for treating tuberculosis, preferably, the invention provides a combined use of the nintedanib or the pharmaceutical salt thereof and other anti-tuberculosis medicines for treating tuberculosis, or an auxiliary medicine for treating tuberculosis. Wherein the other antituberculous drugs are selected from rifampicin, isoniazide, pyrazinamide, ethambutol, fluoroquinolones, streptomycin, kanamycin, amikacin, capreomycin, sodium p-aminosalicylate, ethionamide, cycloserine, clofazimine and linezolid.
Owner:BEIJING CHEST HOSPITAL CAPITAL MEDICAL UNIV +1
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