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3-Deoxyglucosone
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。
3-Deoxyglucosone图片
CAS NO:4084-27-9
包装:5mg
市场价:5800元

3-Deoxy-D-glucosone
3-Deoxyglucosone (3-Deoxy-D-glucosone) 是美拉德反应和多元醇途径的反应中间体 (intermediate)。3-Deoxyglucosone 与蛋白质氨基快速反应形成晚期糖基化终产物 (AGEs),例如咪唑啉酮,它是 3-DG 的最特异 AGE。3-Deoxyglucosone 可以与低葡萄糖协同作用以增强GLP-1分泌,可以作为糖尿病生物学检测的标志物。
生物活性

3-Deoxyglucosone (3-Deoxy-D-glucosone) is a reactiveintermediateof the Maillard reaction and the polyol pathway. 3-Deoxyglucosone rapidly reacts with protein amino groups to form advanced glycation end products (AGEs), such as imidazolone, it is the most specific AGE for 3-DG. 3-Deoxyglucosone synergizes with low glucose to potentiateGLP-1secretion and is considered as a biomarker for diabetes[1][2][3].

体外研究
(In Vitro)

3-Deoxyglucosone (80 ng/ml-1000 ng/ml; 1 hour) markedly increases GLP-1 secretion by 1.23-folds in 300 ng/ml or 1000 ng/ml 3DG-treated group. But at alower concentration (80 ng/ml) has no effects[1].
3-Deoxyglucosone (300 ng/ml; 1 hour) dramatically increases intracellular Ca2+levels by Fluo-3/AM determination (2.5 μM for 30 mins). But 3DG does not affect intracellular cAMP levels in a cAMP Elisa assay[1].
3-Deoxyglucosone (300 ng/ml; 1 hour) significantly increases the protein expression levels of TAS1R2, TAS1R3, and TRPM5 under both glucose-free and highconditions[1].

Western Blot Analysis[1]

Cell Line:STC-1 cells
Concentration:300 ng/ml
Incubation Time:1 hour
Result:Upregulated TAS1R2, TAS1R3, and TRPM5 expression.
体内研究
(In Vivo)

3-Deoxyglucosone (intragastric administration; 20 mg/kg; single dose) impairs glucose tolerance with increased AUC, but the plasma glucagon levels are not significantly different. It developes impaired glucose regulation (IGR) with obviously pancreatic islet cell dysfunction in kunming mice and SD-rats[2].
3-deoxyglucosone (gastric gavage; 5-50 mg/kg; once daily; 2 weeks) is significantly increased in the upper small intestine (1.4-fold), lower small intestine (1.4-fold), ileum (1.4-fold) and colon (two fold) compared with the basal levels in the corresponding control group. In addition, the protein expressions of TAS1R2, TAS1R3 and TRPM5 in both duodenum and colon are significantly decreased[3].

Animal Model:SD rats[3]
Dosage:5, 20 and 50 mg/kg
Administration:oral administration; once daily; 2 weeks
Result:Was capable of accumulating in intestinal tissue and thereby decreased secretion of GLP-1 and insulin.
分子量

162.14

Formula

C6H10O5

CAS 号

4084-27-9

结构分类
  • Saccharides
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.

 
 
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