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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
10MG ¥1131 有现货
25MG ¥1832 有现货
50MG ¥3125 有现货
100MG ¥4311 有现货
200MG ¥5994 有现货
500MG 获取报价 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥803 有现货

生物学信息

  • 产品名称
    Demeclocycline
  • 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
  • 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。
  • 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.
  • 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.
  • 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.
  • 同义词
    ——
  • 通路
    GPCR/G Protein
  • 靶点
    Antibacterial
  • 受体
    Antibacterial
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    127-33-3
  • 分子量
    464.85
  • 分子式
    C21H21ClN2O8
  • 纯度
    >98% (HPLC)
  • 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 )
  • 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
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 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.?
产品手册
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