货号:A468233
同义名:
头孢噻肟钠
/ Cefotaxim sodium; HR-756 sodium
Cefotaxime sodium是一种第三代头孢菌素类抗生素,通过结合青霉素结合蛋白(PBPs)抑制肽聚糖合成终末转肽反应,破坏细胞壁完整性。Cefotaxime sodium具有强β-内酰胺酶稳定性,常用于农杆菌介导转化实验及与万古霉素联用控制细菌污染,有效浓度(50-500 mg/L)。
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 | The cefotaxime sodium spectrum of activity is very broad and includes many common species and a variety of less frequently isolated pathogens. Cefotaxime was consistently active against Actinobacillus actinomycetemcomitans, Capnocytophaga spp, Eikenella corrodens, Erysipelothrix rhusiopathiae, Pasteurella multocida, Plesiomonas shigelloides, and Fusobacterium nucleatum[3]. The stability of cefotaxime sodium was dependent on the surface area of the excipient in contact with the drug[4]. Ceftriaxone may be more versatile having the additional apparent benefits of reducing other postoperative infections, being less dependent on metronidazole as an adjunct and providing a more effective prophylactic cover against Staphylococcus aureus[5]. Moreover, Ceftriaxone and cefotaxime are both effective in the treatment of bacterial meningitis[6]. |
| Concentration | Treated Time | Description | References | |
| Vibrio vulnificus | 0.05 mg/ml | 8 h | Evaluate the inhibitory activity of cefotaxime alone against V. vulnificus, initial inhibition for 8 h followed by regrowth | Antimicrob Agents Chemother. 1997 Oct;41(10):2214-7 |
| Vibrio vulnificus | 0.03 mg/ml | 2 h | Evaluate the inhibitory activity of cefotaxime alone against V. vulnificus, initial inhibition for 2 h followed by regrowth | Antimicrob Agents Chemother. 1997 Oct;41(10):2214-7 |
| Salmonella Typhimurium 14028s | 0.065 mg/l | 3 h | Evaluate the effect of sub-inhibitory concentration of cefotaxime on bacterial survival, results showed a 5-6 fold decrease in survival of bacteria exposed to cefotaxime | Open Biol. 2015 Oct;5(10):150070 |
| Aeromonas veronii C4 | 5 µg/ml | 11 h | To investigate the effect of tmRNA deletion on persister formation to cefotaxime, results showed that tmRNA deletion significantly increased persister cell production. | Front Cell Infect Microbiol. 2020 Feb 28;10:44 |
| Administration | Dosage | Frequency | Description | References | ||
| CBA female mice | Urinary tract infection model | Subcutaneous injection | 100 mg/kg | Every 2 or 4 hours for 24 hours | Evaluate the efficacy of cefotaxime in a urinary tract infection model, showing that the combination of cefotaxime and amoxicillin-clavulanate was effective against CTX-M-15-type ESBL-producing E. coli strains | Antimicrob Agents Chemother. 2015 Nov 2;60(1):424-30 |
| Sprague-Dawley rats | Neonatal rat experimental Escherichia coli sepsis model | Subcutaneous injection | 50 mg/kg | Administered at 7.5 h and 24 h postinoculation | To compare the neuroprotective effects of cefotaxime combined with moxifloxacin versus cefotaxime combined with gentamicin in preventing white matter damage in a neonatal rat model of experimental Escherichia coli sepsis. Results showed that the cefotaxime-moxifloxacin combination significantly reduced microglial activation and immature oligodendrocyte cell death and delayed myelination. | Antimicrob Agents Chemother. 2011 Jul;55(7):3567-9 |
| BALB/c mice | Systemic infection model | Intraperitoneal injection | 0.065 mg/L | Single injection, evaluated after 48 hours of infection | Evaluate the effect of sub-inhibitory concentration of cefotaxime on systemic colonization, results showed enhanced colonization in liver and spleen for bacteria exposed to cefotaxime | Open Biol. 2015 Oct;5(10):150070 |
| BALB/c mice | Peritonitis mouse model | Intraperitoneal injection | 150 mg/kg | Twice daily for 36 hours | Evaluation of the efficacy of mecillinam and cefotaxime combination therapy against CTX-M-15 WT and N135D mutant, showing significant reduction in bacterial load in liver and spleen | Nat Commun. 2019 Feb 6;10(1):618 |
| NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
| NCT03067805 | Sexual Infidelity ... 展开 >> Emotional Infidelity Jealousy 收起 << | Not Applicable | Recruiting | November 2019 | China, Sichuan ... 展开 >> School of Life Science and Technology, University of Electronic Science and Technology Recruiting Chengdu, Sichuan, China, 611731 Contact: Qin Li, Master helenlee@uestc.edu.cn 收起 << |
| NCT03053401 | Post-operative Pain ... 展开 >> Quadriceps Muscle Strength 收起 << | Not Applicable | Recruiting | June 30, 2019 | United States, Ohio ... 展开 >> Akron Children's Hospital Recruiting Akron, Ohio, United States, 44308 Contact: Rami E Karroum, MD 330-543-8823 rkarroum@chmca.org Contact: Ibrahim Farid, MD 330-543-8823 ifarid@chmca.org Sub-Investigator: Ibrahim Farid, MD Sub-Investigator: Paul Fleissner, MD Sub-Investigator: Elizabeth Kendrick, MSN,RN Sub-Investigator: Jonathan Klein, DO Sub-Investigator: George Youssef, MD 收起 << |
| NCT00726622 | Colorectal Cancer | Phase 3 | Active, not recruiting | - | - |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.09mL 0.42mL 0.21mL |
10.47mL 2.09mL 1.05mL |
20.94mL 4.19mL 2.09mL |
|
| CAS号 | 64485-93-4 |
| 分子式 | C16H16N5NaO7S2 |
| 分子量 | 477.45 |
| SMILES Code | O=C([O-])C(N1[C@@]([H])([C@@H](C1=O)NC(/C(C2=CSC(N)=N2)=N/OC)=O)SC3)=C3COC(C)=O.[Na+] |
| MDL No. | MFCD00079073 |
| 别名 | 头孢噻肟钠 ;Cefotaxim sodium; HR-756 sodium; CTX; Cefotaxime(sodium salt); HR-756; Cefotaxime(sodium) |
| 运输 | 蓝冰 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, inert atmosphere, 2-8°C |
| 溶解方案 |
DMSO: 45 mg/mL(94.25 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: 50 mg/mL(104.72 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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