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  1. GPCR/G Protein
  2. GLP Receptor
  3. 3-Deoxyglucosone

3-Deoxyglucosone  (Synonyms: 3-Deoxy-D-glucosone)

目錄號(hào): HY-N7426
產(chǎn)品使用指南

3-Deoxyglucosone (3-Deoxy-D-glucosone) 是美拉德反應(yīng)和多元醇途徑的反應(yīng)中間體 (intermediate)。3-Deoxyglucosone 與蛋白質(zhì)氨基快速反應(yīng)形成晚期糖基化終產(chǎn)物 (AGEs),例如咪唑啉酮,它是 3-DG 的最特異 AGE。3-Deoxyglucosone 可以與低葡萄糖協(xié)同作用以增強(qiáng) GLP-1 分泌,可以作為糖尿病生物學(xué)檢測(cè)的標(biāo)志物。

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3-Deoxyglucosone Chemical Structure

3-Deoxyglucosone Chemical Structure

CAS No. : 4084-27-9

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  • 生物活性

  • 純度 & 產(chǎn)品資料

  • 參考文獻(xiàn)

生物活性

3-Deoxyglucosone (3-Deoxy-D-glucosone) is a reactive intermediate of 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 potentiate GLP-1 secretion and is considered as a biomarker for diabetes[1][2][3].

體外研究
(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].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[1]

Cell Line: STC-1 cells
Concentration: 300?ng/ml
Incubation Time: 1 hour
Result: Upregulated TAS1R2, TAS1R3, and TRPM5 expression.
體內(nèi)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].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

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 號(hào)
結(jié)構(gòu)分類
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運(yùn)輸條件

Room temperature in continental US; may vary elsewhere.

儲(chǔ)存方式

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

純度 & 產(chǎn)品資料
參考文獻(xiàn)
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3-Deoxyglucosone
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