194794-47-3 Usage
Uses
Used in Medicinal Chemistry:
(2S,8S,14S,15S)-5,13-dimethoxy-12-methyl-2,8-diphenyl-3,4-dihydro-2H,14H-8,14-methanochromeno[7,8-d][1,3]benzodioxocine-11,15-diol is used as a potential candidate for drug development due to its complex structure and the presence of multiple functional groups. Its unique stereochemistry and the chromeno and benzodioxocine ring systems may contribute to its biological activity, making it a promising molecule for further research and development in the field of medicinal chemistry.
Used in Pharmacology:
(2S,8S,14S,15S)-5,13-dimethoxy-12-methyl-2,8-diphenyl-3,4-dihydro-2H,14H-8,14-methanochromeno[7,8-d][1,3]benzodioxocine-11,15-diol is used as a subject of study in pharmacology to explore its potential therapeutic effects and mechanisms of action. The molecule's structural features may provide insights into its interactions with biological targets, such as receptors, enzymes, or other proteins, which could lead to the discovery of new drugs or therapeutic agents.
Used in Chemical Synthesis:
(2S,8S,14S,15S)-5,13-dimethoxy-12-methyl-2,8-diphenyl-3,4-dihydro-2H,14H-8,14-methanochromeno[7,8-d][1,3]benzodioxocine-11,15-diol can be used as a starting material or intermediate in the synthesis of other complex organic molecules. Its unique structure and functional groups may be utilized in the development of novel synthetic routes or as building blocks for the creation of new compounds with potential applications in various fields, such as materials science, pharmaceuticals, or agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 194794-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,7,9 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 194794-47:
(8*1)+(7*9)+(6*4)+(5*7)+(4*9)+(3*4)+(2*4)+(1*7)=193
193 % 10 = 3
So 194794-47-3 is a valid CAS Registry Number.
194794-47-3Relevant academic research and scientific papers
Phenolic group on A-ring is key for dracoflavan B as a selective noncompetitive inhibitor of α-amylase
Toh, Zhi Siang,Wang, Hongyu,Yip, Yew Mun,Lu, Yuyun,Lim, Benedict Jeffrey Ang,Zhang, Daiwei,Huang, Dejian
, p. 7641 - 7649 (2015/12/18)
A high throughput assay was applied to guide the isolation of a new pancreatic α-amylase inhibitor, dracoflavan B, from the dragon's blood resin from Daemonorops draco. Applying C18 column, we successfully isolated both diastereomers and their structures
