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Sigma货号R3501现货Rifampicin利福平136

11631389上海睿安生物
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  • ¥10487.32
  • Sigma-Aldrich
  • made in USA
  • R3501
  • 2025年12月10日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      -20°C

    • 保质期

      1年

    • 英文名

      Rifampicin

    • 库存

      100⁺瓶

    • 供应商

      上海睿安生物13611631389

    • CAS号

      13292-46-1

    • 规格

      5g/瓶

    Sigma货号R3501现货Rifampicin利福平13611631389上海睿安生物

    说明

    一般描述:化学结构:大环内酯物

    应用:利福平用于治疗结核病和与结核病相关的分枝杆菌感染。 其广泛应用于自身免疫性胆汁淤积性肝病,原发性胆汁性肝硬化(PBC)的止痒剂。 它已被证明会引起肝炎。

    生化/生理作用

    利福平抑制DNA和蛋白质组装成成熟的病毒颗粒。 它通过与RNA聚合酶的亚基结合抑制RNA合成的起始,从而导致细胞死亡。
    作用方式:通过与RNA聚合酶的β-亚基结合抑制RNA合成的起始。
    抑制DNA和蛋白质组装成成熟的病毒颗粒。

    其他说明:保持容器密闭在干燥通风处。产品对光和湿度敏感。储存在惰性气体中。干燥处保存

     产品细节图片1

    同行评审论文

    Hepatitis and liver dysfunction with rifampicin therapy for pruritus in primary biliary cirrhosis.
    M I Prince et al.
    Gut, 50(3), 436-439 (2002-02-13)
    There is evidence to suggest that rifampicin is an effective second line therapy for controlling pruritus in patients with chronic cholestatic liver disease. It is most widely used as an antipruritic agent in the autoimmune cholestatic liver disease, primary biliary
    Potential market for novel tuberculosis diagnostics: worth the investment?
    Sandra V Kik et al.
    The Journal of infectious diseases, 211 Suppl 2, S58-S66 (2015-03-15)
    The potential available market (PAM) for new diagnostics for tuberculosis that meet the specifications of the high-priority target product profiles (TPPs) is currently unknown. We estimated the PAM in 2020 in 4 high-burden countries (South Africa, Brazil, China, and India)
    In vivo selection of reduced susceptibility to carbapenems in Acinetobacter baumannii related to ISAba1-mediated overexpression of the natural bla(OXA-66) oxacillinase gene.
    Samy Figueiredo et al.
    Antimicrobial agents and chemotherapy, 53(6), 2657-2659 (2009-03-25)
    Two clonally related Acinetobacter baumannii isolates, A1 and A2, were obtained from the same patient. Isolate A2, selected after an imipenem-containing treatment, showed reduced susceptibility to carbapenems. This resistance pattern was related to insertion of the ISAba1 element upstream of
    Linezolid alone or combined with rifampin against methicillin-resistant Staphylococcus_aureus in experimental foreign-body infection.
    Daniela Baldoni et al.
    Antimicrobial agents and chemotherapy, 53(3), 1142-1148 (2008-12-17)
    We investigated the activity of linezolid, alone and in combination with rifampin (rifampicin), against a methicillin-resistant Staphylococcus_aureus(MRSA) strain in vitro and in a guinea pig model of foreign-body infection. The MIC, minimal bactericidal concentration (MBC) in logarithmic phase
    Efficiency and safety of the combination of moxifloxacin, pretomanid (PA-824), and pyrazinamide during the first 8 weeks of antituberculosis treatment: a phase 2b, open-label, partly randomised trial in patients with drug-susceptible or drug-resistant pulmonary tuberculosis.
    Rodney Dawson et al.
    Lancet (London, England), 385(9979), 1738-1747 (2015-03-22)
    New antituberculosis regimens are urgently needed to shorten tuberculosis treatment. Following on from favourable assessment in a 2 week study, we investigated a novel regimen for efficacy and safety in drug-susceptible and multidrug-resistant (MDR) tuberculosis during the first 8 weeks

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    图标文献和实验
    该产品被引用文献

    Sigma货号R3501现货Rifampicin利福平13611631389上海睿安生物

    说明

    一般描述:化学结构:大环内酯物

    应用:利福平用于治疗结核病和与结核病相关的分枝杆菌感染。 其广泛应用于自身免疫性胆汁淤积性肝病,原发性胆汁性肝硬化(PBC)的止痒剂。 它已被证明会引起肝炎。

    生化/生理作用

    利福平抑制DNA和蛋白质组装成成熟的病毒颗粒。 它通过与RNA聚合酶的亚基结合抑制RNA合成的起始,从而导致细胞死亡。
    作用方式:通过与RNA聚合酶的β-亚基结合抑制RNA合成的起始。
    抑制DNA和蛋白质组装成成熟的病毒颗粒。

    其他说明:保持容器密闭在干燥通风处。产品对光和湿度敏感。储存在惰性气体中。干燥处保存

     引用文献图片1

    同行评审论文

    Hepatitis and liver dysfunction with rifampicin therapy for pruritus in primary biliary cirrhosis.
    M I Prince et al.
    Gut, 50(3), 436-439 (2002-02-13)
    There is evidence to suggest that rifampicin is an effective second line therapy for controlling pruritus in patients with chronic cholestatic liver disease. It is most widely used as an antipruritic agent in the autoimmune cholestatic liver disease, primary biliary
    Potential market for novel tuberculosis diagnostics: worth the investment?
    Sandra V Kik et al.
    The Journal of infectious diseases, 211 Suppl 2, S58-S66 (2015-03-15)
    The potential available market (PAM) for new diagnostics for tuberculosis that meet the specifications of the high-priority target product profiles (TPPs) is currently unknown. We estimated the PAM in 2020 in 4 high-burden countries (South Africa, Brazil, China, and India)
    In vivo selection of reduced susceptibility to carbapenems in Acinetobacter baumannii related to ISAba1-mediated overexpression of the natural bla(OXA-66) oxacillinase gene.
    Samy Figueiredo et al.
    Antimicrobial agents and chemotherapy, 53(6), 2657-2659 (2009-03-25)
    Two clonally related Acinetobacter baumannii isolates, A1 and A2, were obtained from the same patient. Isolate A2, selected after an imipenem-containing treatment, showed reduced susceptibility to carbapenems. This resistance pattern was related to insertion of the ISAba1 element upstream of
    Linezolid alone or combined with rifampin against methicillin-resistant Staphylococcus_aureus in experimental foreign-body infection.
    Daniela Baldoni et al.
    Antimicrobial agents and chemotherapy, 53(3), 1142-1148 (2008-12-17)
    We investigated the activity of linezolid, alone and in combination with rifampin (rifampicin), against a methicillin-resistant Staphylococcus_aureus(MRSA) strain in vitro and in a guinea pig model of foreign-body infection. The MIC, minimal bactericidal concentration (MBC) in logarithmic phase
    Efficiency and safety of the combination of moxifloxacin, pretomanid (PA-824), and pyrazinamide during the first 8 weeks of antituberculosis treatment: a phase 2b, open-label, partly randomised trial in patients with drug-susceptible or drug-resistant pulmonary tuberculosis.
    Rodney Dawson et al.
    Lancet (London, England), 385(9979), 1738-1747 (2015-03-22)
    New antituberculosis regimens are urgently needed to shorten tuberculosis treatment. Following on from favourable assessment in a 2 week study, we investigated a novel regimen for efficacy and safety in drug-susceptible and multidrug-resistant (MDR) tuberculosis during the first 8 weeks

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    文献支持
    Sigma货号R3501现货Rifampicin利福平13611631389上海睿安生物
    ¥10487.32