2-(3-Bromophenyl)-5-(trichloromethyl)-1,3,4-oxadiazole | CAS:1020252-87-2
            
            2-(3-Bromophenyl)-5-(trichloromethyl)-1,3,4-oxadiazole
            - 名称:2-(3-溴苯基)-5-(三氯甲基)-1,3,4-恶二唑 | 2-(3-Bromophenyl)-5-(trichloromethyl)-1,3,4-oxadiazole
 - CAS号:1020252-87-2
 - 别名:
 - 分子式:C9H4BrCl3N2O
 - 分子量:342.40
 - EINESC号:
 
产品描述
物理化学性质
| 密度 | 1.788±0.06 g/cm3 (20 º | 
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安全数据
| 没有数据 | 没有数据 | 
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SDS
| 来源 | SDS样本 | 
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| 没有数据 | 没有数据 | 
产品合成路线
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                                        Restoring basal planes of graphene oxides for highly efficient loading and delivery of β-lapachone.Xin Ting Zheng et al.Molecular pharmaceutics, 9(3), 615-621 (2012-01-24)
                                        Effects of β-lapachone, a new anticancer candidate, on cytochrome P450-mediated drug metabolism.In Sook Kim et al.Cancer chemotherapy and pharmacology, 72(3), 699-702 (2013-07-24)
                                        The encapsulation of β-lapachone in 2-hydroxypropyl-β-cyclodextrin inclusion complex into liposomes: a physicochemical evaluation and molecular modeling approach.Isabella M F Cavalcanti et al.European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 44(3), 332-340 (2011-09-06)
                                        Effects of β-lapachone on the production of Th1 and Th2 cytokines in C57BL/6 mice.Myungwon Choi et al.Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer, 31(2), 87-94 (2012-12-12)
                                        Light effect on the stability of β-lapachone in solution: pathways and kinetics of degradation.Marcílio S S Cunha-Filho et al.The Journal of pharmacy and pharmacology, 63(9), 1156-1160 (2011-08-11)
                                        β-Lapachone ameliorization of experimental autoimmune encephalomyelitis.Jihong Xu et al.Journal of neuroimmunology, 254(1-2), 46-54 (2012-09-27)
                                        beta-Lapachone, a novel DNA topoisomerase I inhibitor with a mode of action different from camptothecin.C J Li et al.The Journal of biological chemistry, 268(30), 22463-22468 (1993-10-25)
                                        Smart design of intratumoral thermosensitive β-lapachone hydrogels by Artificial Neural Networks.P Díaz-Rodríguez et al.International journal of pharmaceutics, 433(1-2), 112-118 (2012-05-23)
                                        β-lapachone significantly increases the effect of ionizing radiation to cause mitochondrial apoptosis via JNK activation in cancer cells.Moon-Taek Park et al.PloS one, 6(10), e25976-e25976 (2011-10-15)
                                        NAD(P)H:quinone oxidoreductase 1 (NQO1) in the sensitivity and resistance to antitumor quinones.David Siegel et al.Biochemical pharmacology, 83(8), 1033-1040 (2012-01-03)
                                        Temperature-sensitive gels for intratumoral delivery of β-lapachone: effect of cyclodextrins and ethanol.Marcilio S S Cunha-Filho et al.TheScientificWorldJournal, 2012, 126723-126723 (2012-05-26)
                                        Preclinical genotoxicology of nor-β-lapachone in human cultured lymphocytes and Chinese hamster lung fibroblasts.Bruno C Cavalcanti et al.Chemical research in toxicology, 24(9), 1560-1574 (2011-08-13)
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                                        Beta-lapachone-mediated apoptosis in human promyelocytic leukemia (HL-60) and human prostate cancer cells: a p53-independent response.S M Planchon et al.Cancer research, 55(17), 3706-3711 (1995-09-01)
                                        No role of homologous recombination in dealing with β-lapachone cytotoxicity in yeast.Oliver Quevedo et al.Chemical research in toxicology, 24(12), 2106-2108 (2011-11-19)
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                                        [Cytotoxicity of beta-lapachone, an naphthoquinone with possible therapeutic use].M Dubin et al.Medicina, 61(3), 343-350 (2001-07-28)
                                        An NQO1 substrate with potent antitumor activity that selectively kills by PARP1-induced programmed necrosis.Xiumei Huang et al.Cancer research, 72(12), 3038-3047 (2012-04-26)
                                        Peroxiredoxin 1 knockdown potentiates β-lapachone cytotoxicity through modulation of reactive oxygen species and mitogen-activated protein kinase signals.Tiantian He et al.Carcinogenesis, 34(4), 760-769 (2012-12-15)
                                        Redox cycling of beta-lapachone and structural analogues in microsomal and cytosol liver preparations.Silvia Fernández Villamil et al.Methods in enzymology, 378, 67-87 (2004-03-25)
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                                        Cancer therapy with beta-lapachone.Arthur B Pardee et al.Current cancer drug targets, 2(3), 227-242 (2002-08-22)
                                        beta-Lapachone-induced apoptosis is associated with activation of caspase-3 and inactivation of NF-kappaB in human colon cancer HCT-116 cells.Byung Tae Choi et al.Anti-cancer drugs, 14(10), 845-850 (2003-11-05)
                                        β-lapachone accelerates the recovery of burn-wound skin.Shih-Chen Fu et al.Histology and histopathology, 26(7), 905-914 (2011-06-02)
                                        Endoplasmic reticulum stress-induced JNK activation is a critical event leading to mitochondria-mediated cell death caused by β-lapachone treatment.Hyemi Lee et al.PloS one, 6(6), e21533-e21533 (2011-07-09)
                                        Anti-inflammatory and anti-arthritic activities of 3,4-dihydro-2,2-dimethyl-2H-naphthol[1,2-b]pyran-5,6-dione (β-lapachone).Marília Maria Sitônio et al.Inflammation research : official journal of the European Histamine Research Society ... [et al.], 62(1), 107-113 (2012-10-12)
                                        β-Lapachone analogs with enhanced antiproliferative activity.Carla Ríos-Luci et al.European journal of medicinal chemistry, 53, 264-274 (2012-05-09)
                                        Synthesis of biologically active (-)-dehydroiso-β-lapachone and the determination of its absolute configuration.Tetsutaro Kimachi et al.Chemical & pharmaceutical bulletin, 59(6), 753-756 (2011-06-02)
                                        Screening of anti-cancer agent using zebrafish: comparison with the MTT assay.Yigen Li et al.Biochemical and biophysical research communications, 422(1), 85-90 (2012-05-09)
                                        NQO1 is a determinant for cellular sensitivity to anti-tumor agent Napabucasin.Gaigai Guo et al.American journal of cancer research, 10(5), 1442-1454 (2020-06-09)
                                        Superparamagnetic iron oxide nanoparticles: amplifying ROS stress to improve anticancer drug efficacy.Gang Huang et al.Theranostics, 3(2), 116-126 (2013-02-21)
                                        Cellular DNA Topoisomerases Are Required for the Synthesis of Hepatitis B Virus Covalently Closed Circular DNA.Muhammad Sheraz et al.Journal of virology, 93(11) (2019-03-15)
                                        Ultrastructural analysis of β-lapachone-induced surface membrane damage in male adult Schistosoma mansoni BH strain worms.André de Lima Aires et al.Experimental parasitology, 142, 83-90 (2014-04-29)
                                        Mechanistic studies of cancer cell mitochondria- and NQO1-mediated redox activation of beta-lapachone, a potentially novel anticancer agent.Jason Z Li et al.Toxicology and applied pharmacology, 281(3), 285-293 (2014-12-03)
                                        Photosensitization mechanisms of triplet excited state beta-lapachone. A density functional theory study.Liang Shen Natural product communications, 6(11), 1677-1678 (2012-01-10)
                                        β-Lapachone induces heart morphogenetic and functional defects by promoting the death of erythrocytes and the endocardium in zebrafish embryos.Yi-Ting Wu et al.Journal of biomedical science, 18, 70-70 (2011-09-23)
                                        Synthesis and anti-inflammatory evaluations of β-lapachone derivatives.Chih-Hua Tseng et al.Bioorganic & medicinal chemistry, 21(2), 523-531 (2012-12-13)
                                    
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