货号:A173465
同义名:
磺基水杨酸甲氯环素
/ Meclocycline(Sulfosalicylate Salt)
Meclocycline Sulfosalicylate Salt是一种具有广谱抗菌活性的四环素类抗生素,主要用于预防皮肤细菌感染,如寻常痤疮。


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| 描述 | Meclocycline sulfosalicylate is bacteriostatic and inhibits bacterial protein synthesis by binding to the 30S ribosomal subunit, thereby preventing the addition of amino acids to the growing peptide chain. Meclocycline Sulfosalicylate is a tetracycline antibiotic with broad-spectrum antibacterial activities, preventing skin bacterial infections such as acne vulgaris[1]. Meclocycline is used topically (i.e. for skin infections) as it is totally insoluble in water and may damage kidney and liver if given systemically[2]. Contrary to meclocycline, flunoxaprofen does not possess bactericidal and bacteriostatic properties. Contrary to meclocycline, flunoxaprofen induces a precocious increase of Döderlein bacillus, necessary for a definitive normalization and to limit the possibility of relapses[3]. Meclocycline can produce significant protection of C. elegans from delayed death. Four of the compounds were tested in an ex vivo mouse heart ischemia/reperfusion model and two, meclocycline and 3-amino-1,2,4-triazole, significantly reduced infarction size[4]. |
| Concentration | Treated Time | Description | References | |
| 32D cl 3 cells | 1 µM,10 µM,100 µM | 1 hour | To test the radiation protection and damage mitigation capacity of Meclocycline on 32D cl 3 cells. Results showed no significant effect on cell survival post-irradiation at 1 µM concentration. | In Vivo. 2010 Jan-Feb;24(1):9-19 |
| C. elegans strain gc47;gcSi4 | 100μM | 96 hours | To evaluate the protective effect of Meclocycline against delayed hypoxic injury, results showed that Meclocycline significantly reduced delayed death in C. elegans. | PLoS One. 2017 Apr 20;12(4):e0176061 |
| Administration | Dosage | Frequency | Description | References | ||
| Mice (C57/Bl6) | Langendorff-perfused heart model | Perfusion | 20μM | Continuous administration 30 minutes before ischemia and throughout 60 minutes of reperfusion | To evaluate the protective effect of Meclocycline against cardiac ischemia/reperfusion injury, results showed that Meclocycline significantly reduced infarction size. | PLoS One. 2017 Apr 20;12(4):e0176061 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
1.44mL 0.29mL 0.14mL |
7.19mL 1.44mL 0.72mL |
14.39mL 2.88mL 1.44mL |
|
| CAS号 | 73816-42-9 |
| 分子式 | C29H27ClN2O14S |
| 分子量 | 695.05 |
| SMILES Code | O=C(O)C1=CC(S(=O)(O)=O)=CC=C1O.O=C(C(C2=O)=C(O)[C@@H](N(C)C)[C@]3([H])[C@@H](O)[C@]4([H])C(C5=C(C(C4=C(O)[C@@]32O)=O)C(O)=CC=C5Cl)=C)N |
| MDL No. | MFCD00082372 |
| 别名 | 磺基水杨酸甲氯环素 ;Meclocycline(Sulfosalicylate Salt) |
| 运输 | 蓝冰 |
| InChI Key | WVJKUGVVYXCLFV-CCHMMTNSSA-N |
| Pubchem ID | 54676538 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Inert atmosphere, 2-8°C |
| 溶解方案 |
DMSO: 250 mg/mL(359.69 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 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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