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Targocil {[allProObj[0].p_purity_real_show]}

货号:A377477

Targocil是一种新型抗生素,主要对抗耐甲氧西林金黄色葡萄球菌(MRSA)。

Targocil 化学结构 CAS号:1200443-21-5
Targocil 化学结构
CAS号:1200443-21-5
Targocil 3D分子结构
CAS号:1200443-21-5
Targocil 化学结构 CAS号:1200443-21-5
Targocil 3D分子结构 CAS号:1200443-21-5
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Targocil 纯度/质量文件 产品仅供科研

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Targocil 生物活性

描述 Targocil functions as a bacteriostatic inhibitor of wall teichoic acid (WTA) biosynthesis which can inhibit the growth of methicillin-susceptible S. aureus (MSSA) and methicillin-resistant S. aureus (MRSA) with MIC90s of 2 μg/ mL for both MRSA and MSSA. MICs of Targocil against S. aureus strains Newman, MW2, MG2375, and MG2389 are 1 μg/mL for all strains. Targocil shows excellent activity against S. aureus isolates from suspected cases of bacterial keratitis, including both MSSA and MRSA isolates, with MICs that range from 1 to 2 μg/ mL. Targocil activity was moderately sensitive to the presence of serum, but it inhibited extracellular and intracellular bacteria in the presence of HCECs (human corneal epithelial cells) better than vancomycin. Targocil-resistant strains exhibited a significantly reduced ability to adhere to HCECs[1]. Targocil inhibited intracellular bacteria in the presence of human corneal epithelial cells to a greater extent than vancomycin. Targocil-resistant strains exhibited a significantly reduced ability to adhere to human corneal epithelial cells[2].

Targocil 参考文献

[1]Suzuki T, Swoboda JG, Campbell J, Walker S, Gilmore MS. In vitro antimicrobial activity of wall teichoic acid biosynthesis inhibitors against Staphylococcus aureus isolates. Antimicrob Agents Chemother. 2011;55(2):767‐774

[2]Suzuki T. A new target for Staphylococcus aureus associated with keratitis. Cornea. 2011;30 Suppl 1:S34‐S40

Targocil 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.10mL

0.42mL

0.21mL

10.51mL

2.10mL

1.05mL

21.01mL

4.20mL

2.10mL

Targocil 技术信息

CAS号1200443-21-5
分子式C21H22ClN5O4S
分子量 475.95
SMILES Code COC1=CC2=C(C=C1OC)C(N(CC)CC)=NC3=C(S(=O)(C4=CC=C(Cl)C=C4)=O)N=NN32
MDL No. MFCD19441262
别名
运输蓝冰
InChI Key TYNZGYMGTTUYKZ-UHFFFAOYSA-N
Pubchem ID 44547009
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Inert atmosphere, room temperature

溶解方案

DMSO: 35 mg/mL(73.54 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

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