95343-86-5 Usage
Uses
Used in Pharmaceutical Synthesis:
Alpha-D-Mannopyranosylamine is used as a key intermediate in the synthesis of various pharmaceuticals and biologically active molecules. Its unique structure allows for the creation of compounds with specific therapeutic properties.
Used in Bacterial Infection Treatment:
In the medical field, alpha-D-Mannopyranosylamine is used as a potential treatment for bacterial infections. Its structure enables it to target and combat harmful bacteria, offering a new avenue for antimicrobial therapies.
Used in Drug Delivery Systems:
Alpha-D-Mannopyranosylamine is utilized as a component in drug delivery systems. Its properties allow for the development of innovative methods to transport and release drugs in the body, improving the efficacy and targeting of treatments.
Used in Cancer Research and Treatment:
In oncology, alpha-D-Mannopyranosylamine is studied for its potential anti-cancer properties. Its unique structure may contribute to the development of new cancer therapies, offering hope for more effective treatments.
Used in Carbohydrate-Based Drug Design:
As a building block, alpha-D-Mannopyranosylamine is used in the design of new carbohydrate-based drugs. Its versatile chemical structure provides a foundation for creating novel compounds with specific biological activities, expanding the range of available pharmaceuticals.
Overall, alpha-D-Mannopyranosylamine's diverse applications across various industries highlight its importance in research and development within the pharmaceutical and biotechnology sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 95343-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,3,4 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 95343-86:
(7*9)+(6*5)+(5*3)+(4*4)+(3*3)+(2*8)+(1*6)=155
155 % 10 = 5
So 95343-86-5 is a valid CAS Registry Number.
95343-86-5Relevant academic research and scientific papers
Maity, Sanat K.,Dutta, Samir K.,Banerjee, Asish K.,Achari, Basudeb,Singh, Manoranjan
, p. 6965 - 6974 (1994)
A series of N-, C- and S- mannopyranosyl derivatives (4, 9-16) have been synthesised and their inhibitory activity tested towards jackbean α-mannosidase (EC 3.2.1.24).These compounds are of mechanistic and synthetic interest in the design of new α-mannosidase inhibitors.
Studies on N-Glycopeptides. II. Separation of α- and β-Amide of N-(L-Aspartyl)-β-D-glucopyranosylamine Obtained via N-(Benzyloxycarbonyl)-L-aspartic Anhydride
Tamura, Masahiro,Nishizaki, Hiroshi,Miyazaki, Chiemi,Okai, Hideo
, p. 3167 - 3172 (2007/10/02)
A mixture of N-(L-α-aspartyl)- and N-(L-β-aspartyl)-β-D-glucopyranosylamine was obtained by the condensation of N-(benzyloxycarbonyl)-L-aspartic anhydride with β-D-glucopyranosylamine.Attempts to separate the mixture by using cation-exchange chromatography, a copper(II) complex, and fractional recrystallization were carried out.These separations gave good yields of the desired β-amine.
