Demeclocycline
CAS No. 127-33-3
Demeclocycline ( —— )
产品货号. M33246 CAS No. 127-33-3
Demeclocycline 是一种具有口服活性的四环素类抗生素,通过与 30S 核糖体亚单位结合来抑制氨基酰 tRNA 的结合,从而影响蛋白质的合成。Demeclocycline 对广谱的细菌感染表现出抗菌活性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥727 | 有现货 |
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| 10MG | ¥1131 | 有现货 |
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| 25MG | ¥1832 | 有现货 |
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| 50MG | ¥3125 | 有现货 |
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| 100MG | ¥4311 | 有现货 |
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| 200MG | ¥5994 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥803 | 有现货 |
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生物学信息
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产品名称Demeclocycline
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Demeclocycline 是一种具有口服活性的四环素类抗生素,通过与 30S 核糖体亚单位结合来抑制氨基酰 tRNA 的结合,从而影响蛋白质的合成。Demeclocycline 对广谱的细菌感染表现出抗菌活性。
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产品描述Demeclocycline is an orally active tetracycline antibiotic. Demeclocycline impairs protein synthesis by binding to the 30S ribosomal subunit to inhibit binding of aminoacyl tRNA. Demeclocycline shows anti-bacterial activitise to a wide variety of bacterial infections.
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体外实验Demeclocycline (0-100 μM; 24 h) treatment reduces AQP2 abundance in mpkCCD cells.Demeclocycline (10 μM; 24 h) treatment promotes the activity of monocytes and macrophages.Demeclocycline (1-10 μM; 72 h) treatment directly affects the growth of brain tumorinitiating cells.Western Blot Analysis Cell Line:MpkCCD cells Concentration:0-100 μM Incubation Time:24 hours Result:Decreased AQP2 abundance in mpkCCD cells, with significant effects at 50 μM.Cell Viability Assay Cell Line:mouse bone marrow derived macrophages and monocytes Concentration:10 μM Incubation Time:24 hours Result:Enhanced TNF-α production and modulated monocyte functions.Cell Viability Assay Cell Line:brain tumorinitiating cells Concentration:1, 5, and 10 μM Incubation Time:72 hours Result:Inhibited cells growth in two ways: using monocytes as an intermediary, and directly by affecting the proliferation and sphere-forming capacity of brain tumorinitiating cells.
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体内实验Demeclocycline (Intraperitoneal injection; 40 mg/kg; once daily; 48 h) treatment results in a significant reduction of hyponatremia and a significant correction of the hypoosmolality, and is not nephrotoxic.Animal Model:Male Wistar rats induced with hyponatremia Dosage:40 mg/kg Administration:Intraperitoneal injection; 40 mg/kg; once daily; 48 hours Result:Increased urine volume, decreased urine osmolality, and caused a significantly increased fractional excretion of water.Animal Model:Male Wistar rats induced with hyponatremiaDosage:40 mg/kg Administration:Intraperitoneal injection; 40 mg/kg; once daily; 48 hours Result:Indicated the effect in the renal inner medulla for AQP2 and AC5/6 specifically, and not secondary toxicity effect.
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同义词——
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通路GPCR/G Protein
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靶点Antibacterial
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受体Antibacterial
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研究领域——
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适应症——
化学信息
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CAS Number127-33-3
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分子量464.85
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分子式C21H21ClN2O8
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纯度>98% (HPLC)
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溶解度In Vitro:?H2O 中的溶解度 : 40 mg/mL (86.05 mM; 超声助溶)DMSO 中的溶解度 : 25 mg/mL (53.78 mM; 超声助溶 )
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SMILES[H][C@]12C[C@@]3([H])[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]3(O)C(O)=C1C(=O)c1c(O)ccc(Cl)c1[C@H]2O
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. I Chopra, et al. Tetracyclines, molecular and clinical aspects. J Antimicrob Chemother. 1992 Mar;29(3):245-77.?
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