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3-(1,2,3-trihydroxy-propyl)-quinoxaline-2-carboxylic acid 2-amino-anilide is a complex organic compound with the molecular formula C16H17N3O6. It is a derivative of quinoxaline-2-carboxylic acid, featuring a 2-amino-anilide group attached to the quinoxaline ring. The compound is characterized by the presence of a 1,2,3-trihydroxy-propyl side chain, which contributes to its hydrophilic properties. This chemical structure is of interest in medicinal chemistry, particularly in the development of potential therapeutic agents, due to its ability to form hydrogen bonds and interact with biological targets. The compound's specific applications and pharmacological properties would depend on its ability to engage with specific receptors or enzymes in the body, which could be explored through further research and development.

804-00-2

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804-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 804-00-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,0 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 804-00:
(5*8)+(4*0)+(3*4)+(2*0)+(1*0)=52
52 % 10 = 2
So 804-00-2 is a valid CAS Registry Number.

804-00-2Downstream Products

804-00-2Relevant academic research and scientific papers

Extending the spectrum of α-dicarbonyl compounds in vivo

Henning, Christian,Liehr, Kristin,Girndt, Matthias,Ulrich, Christof,Glomb, Marcus A.

, p. 28676 - 28688 (2014)

Maillard α-dicarbonyl compounds are known as central intermediates in advanced glycation end product (AGE) formation. Glucose is the primary source of energy for the human body, whereas L-threo-ascorbic acid (vitamin C) is an essential nutrient, involved in a variety of enzymatic reactions. Thus, the Maillard degradation of glucose and ascorbic acid is of major importance in vivo. To understand the complex mechanistic pathways of AGE formation, it is crucial to extend the knowledge on plasma concentrations of reactive key α-dicarbonyl compounds (e.g. 1-deoxyglucosone). With the present work, we introduce a highly sensitive LC-MS/MS multimethod for human blood plasma based on derivatization with o-phenylenediamine under acidic conditions. The impact of workup and reaction conditions, particularly of pH, was thoroughly evaluated. A comprehensive validation provided the limit of detection, limit of quantitation, coefficients of variation, and recovery rates. The method includes the α-dicarbonyls 1-deoxyglucosone, 3-deoxyglucosone, glucosone, Lederer's glucosone, dehydroascorbic acid, 2,3-diketogulonic acid, 1-deoxypentosone, 3-deoxypentosone, 3,4-dideoxypentosone, pentosone, 1-deoxythreosone, 3-deoxythreosone, threosone, methylglyoxal, glyoxal; the α-keto-carboxylic acids pyruvic acid and glyoxylic acid; and the dicarboxylic acid oxalic acid. The method was then applied to the analyses of 15 healthy subjects and 24 uremic patients undergoing hemodialysis. The comparison of the results revealed a clear shift in the product spectrum. Inmost cases, the plasma levels of target analytes were significantly higher. Thus, this is the first time that a complete spectrum of α-dicarbonyl compounds relevant in vivo has been established. The results provide further insights into the chemistry of AGE formation and will be helpful to find specific markers to differentiate between the various precursors of glycation.

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