25119-42-0 Usage
Description
6-[2-[3-[[(2R)-4-[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethylsulfanyl]-6-oxohexanoic acid is a complex organic compound with a unique molecular structure that features various functional groups, including amino, hydroxy, and phosphoryl moieties. This molecule is characterized by its stereochemistry, with specific R and S configurations at different carbon centers, which may contribute to its biological activity and potential applications.
Uses
6-[2-[3-[[(2R)-4-[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethylsulfanyl]-6-oxohexanoic acid is used as a metabolically engineered microorganism with improved energetic efficiency for enhancing the production of biofuels and other valuable chemicals through microbial fermentation processes.
Used in Pharmaceutical Industry:
6-[2-[3-[[(2R)-4-[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethylsulfanyl]-6-oxohexanoic acid is used as a potential therapeutic agent for the treatment of various diseases, including cancer, due to its unique molecular structure and the presence of bioactive functional groups that may interact with cellular targets and modulate biological pathways.
Used in Chemical Synthesis:
6-[2-[3-[[(2R)-4-[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethylsulfanyl]-6-oxohexanoic acid can be used as a key intermediate in the synthesis of more complex molecules, such as pharmaceuticals, agrochemicals, and other specialty chemicals, where its unique functional groups and stereochemistry can be exploited to create novel compounds with desired properties and applications.
Used in Research and Development:
6-[2-[3-[[(2R)-4-[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethylsulfanyl]-6-oxohexanoic acid serves as an important research tool in the study of biological processes and the development of new drugs and therapies. Its unique structure and functional groups can be used to probe the mechanisms of action of various enzymes, receptors, and other cellular targets, leading to a better understanding of disease pathways and the identification of new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 25119-42-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,1 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25119-42:
(7*2)+(6*5)+(5*1)+(4*1)+(3*9)+(2*4)+(1*2)=90
90 % 10 = 0
So 25119-42-0 is a valid CAS Registry Number.
25119-42-0Relevant articles and documents
Identification of an α-Oxoamine Synthase and a One-Pot Two-Step Enzymatic Synthesis of α-Amino Ketones
Zhou, Ting,Gao, Du,Li, Jia-Xin,Xu, Min-Juan,Xu, Jun
supporting information, p. 37 - 41 (2020/12/21)
Alb29, an α-oxoamine synthase involved in albogrisin biosynthesis in Streptomyces albogriseolus MGR072, was characterized and responsible for the incorporation of l-glutamate to acyl-coenzyme A substrates. Combined with Alb29 and Mgr36 (an acyl-coenzyme A ligase), a one-pot enzymatic system was established to synthesize seven α-amino ketones. When these α-amino ketones were fed into the alb29 knockout strain Δalb29, respectively, the albogrisin analogs with different side chains were observed.
