ID1140 多利培南一水合物 抗感染 索莱宝

ID1140 多利培南一水合物 抗感染 索莱宝

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  • ¥302 - 1340
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  • 北京
  • ID1140
  • 2025年12月18日
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    • 详细信息
    • 技术资料
    • 保存条件

      Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year

    • 保质期

      Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year

    • 英文名

      Doripenem Monohydrate

    • 库存

      现询

    • 供应商

      北京索莱宝科技有限公司

    • CAS号

      364622-82-2

    • 规格

      25mg/5mg/50mg/10mg

    规格:25mg产品价格:¥800.0
    规格:5mg产品价格:¥302.0
    规格:50mg产品价格:¥1340.0
    规格:10mg产品价格:¥490.0

    是广谱的β-内酰胺抗生素。

    基本信息
    CASNo.364622-82-2
    中文名称多利培南一水合物
    英文名称Doripenem Monohydrate
    别名S-4661
    分子式C15H24N4O6S2·H2O
    分子量438.52
    溶解性Soluble in Water ≥1mg/mL;Soluble in DMSO ≥5mg/mL
    纯度HPLC≥98%
    外观(性状)Light yellow to yellow Solid
    储存条件Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
    ECEINECS 680-392-3
    MDLMFCD09749887
    SMILESO=C(C(N12)=C(S[C@@H]3CN[C@H](CNS(=O)(N)=O)C3)[C@H](C)[C@]2([H])[C@@H]([C@H](O)C)C1=O)O.O
    靶点Bacterial
    通路Anti-infection
    背景说明是广谱的β-内酰胺抗生素。
    生物活性Doripenem (S 4661) monohydrate, a 1β-methyl parenteral carbapenem, has very broad-spectrum activity against Gram-positive and Gram-negative aerobic bacteria[1][2].
    细胞实验The objective of this study was to evaluate simulated human exposures to doripenem using a neutropenic murine thigh infection model against 24 clinical P. aeruginosa isolates with a wide range of MICs.Dosing regimens in mice were designed to approximate the free time above MIC (fT>MIC) observed with 500 mg doripenem every 8 h given as either a 1 - h or 4 - h intravenous infusion in humans.Maximal antibacterial killing was associated with doripenem exposures of > or =40% fT>MIC; bacteriostatic effects were noted at approximately 20% fT>MIC. The simulated 1 - h infusion provided bactericidal effects for isolates with MICs of < or =2 microg/ml, while variable killing was noted for isolates with MICs of 4 to 8 microg/ml and regrowth for isolates with an MIC of 16 microg/ml. The 4 - h infusion regimen displayed similar killing for isolates with MICs of < or =2 microg/ml and enhanced activity for two of the four isolates with an MIC of 4 microg/ml. Given that the 4 - h regimen yields negligible fT>MIC for MICs of > or =8 microg/ml, regrowth was generally observed. Simulated doses of 500 mg doripenem every 8 h infused over 1 h demonstrated antibacterial killing for P. aeruginosa isolates with MICs of 0.125 to 8 microg/ml. Exposures of > or =40% fT>MIC resulted in the most pronounced bactericidal effects, while killing was variable for 20 to 30% fT>MIC. Infusing doses over 4 h enhanced efficacy against selected pseudomonal isolates with an MIC of 4 microg/ml.[1]。Animal Model:Specific-pathogen-free, female ICR mice weighing approximately 25 g with P. aeruginosa-infected thighs[1];Dosage:MIC range of 2 to 16 μg/ml;Administration:Subcutaneous; 1-h and 4-h infusion; 0.2 ml injections;Result: Demonstrated antibacterial killing for P. aeruginosa.
    数据来源文献[1]. Aryun Kim, et al. In vivo pharmacodynamic profiling of doripenem against Pseudomonas aeruginosa by simulating human exposures. Antimicrob Agents Chemother. 2008 Jul;52(7):2497-502.
    [2]. Jones RN, et al. Doripenem (S-4661), a novel carbapenem: comparative activity against contemporary pathogens including bactericidal action and preliminary in vitro methods evaluations. J Antimicrob Chemother. 2004 Jul;54(1):144-54. Epub 2004 Jun 9.
    单位

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