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Demeclocycline
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Demeclocycline图片
CAS NO:127-33-3
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品名称
去甲金霉素
产品介绍
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。
生物活性

Demeclocycline is an orally activetetracyclineantibiotic. 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 ofbacterialinfections[1][2].

IC50& Target

Tetracycline

 

体外研究
(In Vitro)

Demeclocycline (0-100 μM; 24 h) treatment reduces AQP2 abundance in mpkCCD cells[3].
Demeclocycline (10 μM; 24 h) treatment promotes the activity of monocytes and macrophages[4].
Demeclocycline (1-10 μM; 72 h) treatment directly affects the growth of brain tumorinitiating cells[4].

Western Blot Analysis[3]

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[4]

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[4]

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.
体内研究
(In Vivo)

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[3].

Animal Model:Male Wistar rats induced with hyponatremia[3]
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 hyponatremia[3]
Dosage: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.
Clinical Trial
分子量

464.85

Formula

C21H21ClN2O8

CAS 号

127-33-3

中文名称

去甲金霉素

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.