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Meticillin

更新时间:2025-08-25 20:32:40

Meticillin结构式
Meticillin结构式
品牌特惠专场
常用名 Meticillin 英文名 Meticillin
CAS号 61-32-5 分子量 380.41600
密度 N/A 沸点 N/A
分子式 C17H20N2O6S 熔点 N/A
MSDS 中文版 美版 闪点 N/A
符号 GHS07
GHS07
信号词 Warning

 Meticillin用途


甲氧西林是一种窄谱β-内酰胺抗生素,通过抑制青霉素结合蛋白(PBPs)发挥作用。甲氧西林对其他青霉素耐药的金黄色葡萄球菌和表皮葡萄球菌具有活性。甲氧西林可用于研究皮肤感染、骨髓炎和心内膜炎[1]。

 Meticillin名称

英文名 methicillin
英文别名 更多

 Meticillin生物活性

描述 甲氧西林是一种窄谱β-内酰胺抗生素,通过抑制青霉素结合蛋白(PBPs)发挥作用。甲氧西林对其他青霉素耐药的金黄色葡萄球菌和表皮葡萄球菌具有活性。甲氧西林可用于研究皮肤感染、骨髓炎和心内膜炎[1]。
相关类别
体外研究 甲氧西林(20μg/mL,24小时)导致金黄色葡萄球菌的CFU快速下降[2]。
体内研究 金黄色葡萄球菌中的甲氧西林(肌肉注射,每6小时,5天40毫克/公斤)-受感染的兔子[2]。
参考文献

[1]. Sharon S. Castle. Methicillin. xPharm: The Comprehensive Pharmacology Reference 2007, Pages 1-4.

[2]. Jaime Carrizosa, et al. Treatment of Experimental Staphylococcus aureus Endocarditis: Comparison of Cephalothin, Cefazolin, and Methicillin. Antimicrob Agents Chemother. 1978 Jan; 13(1): 74–77.

 Meticillin物理化学性质

分子式 C17H20N2O6S
分子量 380.41600
精确质量 380.10400
PSA 130.47000
LogP 1.27790
InChIKey RJQXTJLFIWVMTO-TYNCELHUSA-N
SMILES COc1cccc(OC)c1C(=O)NC1C(=O)N2C1SC(C)(C)C2C(=O)O

 Meticillin安全信息

符号 GHS07
GHS07
信号词 Warning
危害声明 H302
个人防护装备 dust mask type N95 (US);Eyeshields;Gloves
危险品运输编码 NONH for all modes of transport
RTECS号 XH8930000

 Meticillin上下游产品

Meticillin上游产品  0

Meticillin下游产品  1

 Meticillin文献91

更多文献
Antimicrobial properties of membrane-active dodecapeptides derived from MSI-78.

Biochim. Biophys. Acta 1848(5) , 1139-46, (2015)

Antimicrobial peptides (AMPs) are a class of broad-spectrum antibiotics known by their ability to disrupt bacterial membranes and their low tendency to induce bacterial resistance, arising as excellen...

Bacteriophage as effective decolonising agent for elimination of MRSA from anterior nares of BALB/c mice.

BMC Microbiol. 14 , 212, (2014)

Nasal carriers not only pose serious threat to themselves but also to the community by playing an active role in the dissemination of serious and life threatening S. aureus especially MRSA strains. Th...

Preparation and in vitro-in vivo evaluation of ofloxacin loaded ophthalmic nano structured lipid carriers modified with chitosan oligosaccharide lactate for the treatment of bacterial keratitis.

Eur. J. Pharm. Sci. 63 , 204-15, (2014)

The objective of this study was to explore the potential of the nanostructured lipid carriers (NLCs) modified with chitosan oligosaccharide lactate (COL) for topical ocular application. Ofloxacin (OFX...

 Meticillin靶点实验

查看更多实验

实验名称:Compound was tested for antibacterial activity against MRSA ATCC 33591, expressed as ...
来源:ChEMBL
靶标:Staphylococcus aureus
External Id:CHEMBL807331
实验名称:Induction of drug resistance in Staphylococcus aureus ATCC 29213 at 0.1 times MIC mea...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL5333131
实验名称:Antibacterial activity against Staphylococcus aureus MRSA198 clinical isolate-1 measu...
来源:ChEMBL
靶标:Staphylococcus aureus
External Id:CHEMBL4391053
实验名称:Antibacterial activity against Staphylococcus aureus MRSA198 clinical isolate-2 measu...
来源:ChEMBL
靶标:Staphylococcus aureus
External Id:CHEMBL4391054
实验名称:Antibacterial activity against Staphylococcus aureus MRSA198 clinical isolate-3 measu...
来源:ChEMBL
靶标:Staphylococcus aureus
External Id:CHEMBL4391055
实验名称:Antibacterial activity against Bacillus subtilis ATCC 11774 after 18 to 20 hrs by mic...
来源:ChEMBL
靶标:Bacillus subtilis
External Id:CHEMBL4391046
实验名称:Antibacterial activity against Staphylococcus aureus ATCC 11632 after 18 to 20 hrs by...
来源:ChEMBL
靶标:Staphylococcus aureus
External Id:CHEMBL4391047
实验名称:Antibacterial activity against Staphylococcus epidermidis ATCC 12228 after 18 to 20 h...
来源:ChEMBL
靶标:Staphylococcus epidermidis
External Id:CHEMBL4391048
实验名称:Antibacterial activity against Escherichia coli ATCC 25922 measured after 18 to 20 hr...
来源:ChEMBL
靶标:Escherichia coli
External Id:CHEMBL4391049
实验名称:Antibacterial activity against measured after Klebsiella pneumoniae ATCC 4352 measure...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4391050
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 Meticillin英文别名

Meticillin
meticillin
6β-(2,6-dimethoxy-benzoylamino)-penicillanic acid
METICILLIN
6-(2,6-dimethoxybenzamido)penicillinic acid
(2S,5R,6R)-6-[(2,6-dimethoxybenzoyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
Methicillin
methycillin
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