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Meropenem Trihydrate/美罗培南三水合物 {[allProObj[0].p_purity_real_show]}

货号:A188476 同义名: 美罗培南三水合物 / SM 7338 trihydrate; Meropenem (hydrate)

Meropenem Trihydrate是一种广谱抗生素,用于研究各种由革兰氏阳性和革兰氏阴性细菌引起的感染。

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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Meropenem Trihydrate/美罗培南三水合物 化学结构 CAS号:119478-56-7
Meropenem Trihydrate/美罗培南三水合物 化学结构
CAS号:119478-56-7
Meropenem Trihydrate/美罗培南三水合物 3D分子结构
CAS号:119478-56-7
Meropenem Trihydrate/美罗培南三水合物 化学结构 CAS号:119478-56-7
Meropenem Trihydrate/美罗培南三水合物 3D分子结构 CAS号:119478-56-7
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Meropenem Trihydrate/美罗培南三水合物 纯度/质量文件 产品仅供科研

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Meropenem Trihydrate/美罗培南三水合物 生物活性

描述 Meropenem Trihydrate is a novel carbapenem antibiotic for injection[3]. Meropenem, like imipenem and various experimental penems, may overcome the resistance problems presented by Class I beta-lactamases[4]. Antibacterial drugs significantly inhibit hPON1 activity with rank order meropenem trihydrate piperacillin sodium cefoperazone sodium in vitro[5]. Meropenem can cause severe liver injury and that early recognition of drug-induced liver injury is important[6]. Moreover, the antimicrobial activity of meropenem irradiated with the dose of 25 kGy was unchanged. Radiostelization is a promising, alternative method for obtaining sterile meropenem[7].

Meropenem Trihydrate/美罗培南三水合物 细胞实验

Cell Line
Concentration Treated Time Description References
Red blood cells 1000 mg/mL Evaluate hemolytic activity, results showed no hemolysis even at 1000 mg/mL concentration. Acta Pharm Sin B. 2021 Jan;11(1):203-221
NDM-1-negative E. coli 0.03 µg mL−1 24 hours Evaluate the antibacterial activity of Meropenem against NDM-1-negative E. coli, showing an MIC of 0.03 µg mL−1 Nat Commun. 2018 Jan 30;9(1):439
NDM-1-positive E. coli 16 µg mL−1 24 hours Evaluate the antibacterial activity of Meropenem against NDM-1-positive E. coli, showing an MIC of 16 µg mL−1 Nat Commun. 2018 Jan 30;9(1):439

Meropenem Trihydrate/美罗培南三水合物 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
BALB/c mice Sepsis mouse model Subcutaneous injection 10 mg/kg (MEM), 30 mg/kg (19bh) Single dose, monitored for 96 hours Evaluate the in vivo efficacy of compound 19bh combined with MEM, results showed that the combination treatment was markedly effective in treating infections caused by NDM-1 positive strain and prolonged the survival time of sepsis mice. Acta Pharm Sin B. 2021 Jan;11(1):203-221
BALB/c mice Peritonitis model Intraperitoneal injection 5 mg/kg Twice daily until the endpoint of the experiment Evaluate the efficacy of Meropenem and CBS combination therapy in mice infected with NDM-1-positive bacteria, showing a significant increase in survival rate Nat Commun. 2018 Jan 30;9(1):439
Mice Allogeneic hematopoietic stem cell transplantation (allo-HSCT) model Oral (drinking water) 0.625 g/L (drinking water) Daily, from day 3 to day 15 post-transplantation To study the effect of meropenem on GVHD, finding that meropenem treatment aggravates colonic GVHD, leading to thinning of the colonic mucus layer and bacterial translocation Cell. 2022 Sep 29;185(20):3705-3719. e14
Mice Escherichia coli sepsis model Intravenous injection 10 mg/kg Single dose at 2 or 8 hours post-infection To evaluate the effect of Meropenem on the sepsis model, results showed that Meropenem significantly reduced bacterial load in heart, lung, and kidney, but had less effect on spleen and liver. Nat Commun. 2023 Jun 17;14(1):3603
C57BL/6 mice Pneumonia and bacteremia models Meropenem subcutaneously, mAbs intravenously Meropenem: 7.5 mg/kg (O1 strain) or 50 mg/kg (O2 strain); mAbs: 1 mg/kg (KPE33) or 0.2 mg/kg (KPN42) Administered 1 hour post-infection, survival monitored daily Evaluate synergistic therapeutic effect of anti-O antigen mAbs with meropenem, showing combination therapy significantly improved survival against resistant strains. Nat Commun. 2017 Dec 8;8(1):1991
Mice Tissue cage implant infection model Intraperitoneal injection 100 mg/kg Once daily for 10 days Evaluate the efficacy of Meropenem combined with phage Paride in chronic infections. Results showed that the combination significantly reduced bacterial loads. Nat Commun. 2024 Jan 2;15(1):175
Swiss Webster mice Gestational sepsis model Subcutaneous injection 10 mg/kg After 5 h, 24 h, 48 h, and 72 h To evaluate the therapeutic effect of meropenem on gestational sepsis and its impact on offspring. Results showed that meropenem treatment alleviated sepsis symptoms, but offspring still exhibited abnormalities in neurodevelopment and behavior. J Neuroinflammation. 2021 Feb 25;18(1):60
Mice Antibiotic-induced gut dysbiosis model Oral gavage 21.6 mg Twice daily (days 0-6), once daily (days 7-11), for 11 days To investigate the effects of antibiotic-induced gut dysbiosis on cognitive function. Results showed that meropenem, in combination with other antibiotics, significantly altered gut microbiota composition, reduced bacterial metabolite levels in the colon and plasma, and impaired novel object recognition memory in mice. Brain Behav Immun. 2016 Aug;56:140-55
Mice Pseudomonas aeruginosa keratitis model Topical administration 0.5 mg/mL Every 8 hours for 72 hours To evaluate the efficacy of meropenem in combination with LasB inhibitor (R)-30 for treating Pseudomonas aeruginosa keratitis. Results showed that the combination significantly reduced bacterial load and clinical symptoms, outperforming meropenem alone. Adv Sci (Weinh). 2025 Apr;12(14):e2411807

Meropenem Trihydrate/美罗培南三水合物 临床研究

NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT01551394 Sepsis Phase 3 Completed - Italy ... 展开 >> Ursula TRAFOJER Padova, Italy, 35128 收起 <<
NCT01554124 Meningitis Phase 1 Phase 2 Completed - United Kingdom ... 展开 >> HEATH, Paul London, Cranmer Terrace, United Kingdom, SW17 ORE 收起 <<

Meropenem Trihydrate/美罗培南三水合物 参考文献

[1]Slaney L, Chubb H, et al., In-vitro activity of meropenem against Neisseria gonorrhoeae, Haemophilus influenzae and H. ducreyi from Canada and Kenya. J Antimicrob Chemother, 1989. 24 Suppl A: p. 183-6.

[2]Voutsinas D, Mavroudis T, et al. In-vitro activity of meropenem, a new carbapenem, against multiresistant Pseudomonas aeruginosa compared with that of other antipseudomonal antimicrobials. J Antimicrob Chemother. 1989 Sep;24 Suppl A:143-7.

[3]Takeuchi Y, Takebayashi Y, Sunagawa M, Isobe Y, Hamazume Y, Uemura A, Noguchi T. The stability of a novel carbapenem antibiotic, meropenem (SM-7338), in a solid state formulation for injection. Chem Pharm Bull (Tokyo). 1993 Nov;41(11):1998-2002. doi: 10.1248/cpb.41.1998. PMID: 8293523.

[4]Yang YJ, Livermore DM. Interactions of meropenem with class I chromosomal beta-lactamases. J Antimicrob Chemother. 1989 Sep;24 Suppl A:207-17. doi: 10.1093/jac/24.suppl_a.207. PMID: 2808208.

[5]Söyüt H, Kaya ED, Beydemir S. Impact of antibacterial drugs on human serum paraoxonase-1 (hPON1) activity: an in vitro study. Asian Pac J Trop Biomed. 2014 Aug;4(8):603-9. doi: 10.12980/APJTB.4.2014APJTB-2014-0059. PMID: 25183328; PMCID: PMC4037652.

[7]Kilińska K, Cielecka-Piontek J, Skibiński R, Szymanowska D, Miklaszewski A, Bednarski W, Tykarska E, Stasiłowicz A, Zalewski P. The Radiostability of Meropenem Trihydrate in Solid State. Molecules. 2018 Oct 23;23(11):2738. doi: 10.3390/molecules23112738. PMID: 30360551; PMCID: PMC6278425.

Meropenem Trihydrate/美罗培南三水合物 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.29mL

0.46mL

0.23mL

11.43mL

2.29mL

1.14mL

22.86mL

4.57mL

2.29mL

Meropenem Trihydrate/美罗培南三水合物 技术信息

CAS号119478-56-7
分子式C17H31N3O8S
分子量 437.51
SMILES Code O=C(C(N12)=C(S[C@@H]3CN[C@H](C(N(C)C)=O)C3)[C@H](C)[C@]2([H])[C@@H]([C@H](O)C)C1=O)O.[H]O[H].[H]O[H].[H]O[H]
MDL No. MFCD08600005
别名 美罗培南三水合物 ;SM 7338 trihydrate; Meropenem (hydrate); SM-7338; ICI 194660
运输蓝冰
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Inert atmosphere, store in freezer, under -20°C

溶解方案

DMSO: 105 mg/mL(239.99 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 12 mg/mL(27.43 mM),配合低频超声助溶

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
方案 一
方案 二
方案 三
配制的工作液建议现用现配,短期内尽快用完。 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
方案 一
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