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。
HazMat Fee + There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.
| 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+ |


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|---|---|---|---|---|---|---|---|
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| 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]. |
| 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 |
| 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 |
| 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 << |
| 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 |
|
| 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 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
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