40372-09-6 Usage
Description
O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1→6)-O-[6-deoxy-6-[[(phenylMethoxy)carbonyl]amino]-α-D-glucopyranosyl-(1→4)]-2-deoxy-D-streptaMine is a complex carbohydrate derivative with a unique chemical structure. It is characterized by its pale yellow solid appearance and is composed of multiple sugar units linked together in a specific arrangement. The molecule features an amino group at the 3-position of the first sugar unit and a deoxy sugar unit at the 2-position of the streptamine core. Additionally, it contains a phenylmethoxycarbonyl group attached to the 6-position of the second sugar unit, which may contribute to its chemical properties and potential applications.
Uses
Used in Pharmaceutical Industry:
O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1→6)-O-[6-deoxy-6-[[(phenylMethoxy)carbonyl]amino]-α-D-glucopyranosyl-(1→4)]-2-deoxy-D-streptaMine is used as an intermediate in the synthesis of various pharmaceutical compounds, such as antibiotics and antiviral drugs. Its unique structure and functional groups make it a valuable building block for the development of new therapeutic agents.
Used in Chemical Synthesis:
In the field of organic chemistry, this complex carbohydrate derivative can be used as a starting material for the synthesis of a wide range of compounds with potential applications in various industries. Its versatility in chemical reactions, such as glycosylation and amide formation, allows for the creation of novel molecules with tailored properties.
Used in Research and Development:
Due to its structural complexity and unique features, O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1→6)-O-[6-deoxy-6-[[(phenylMethoxy)carbonyl]amino]-α-D-glucopyranosyl-(1→4)]-2-deoxy-D-streptaMine can be employed in research and development efforts to study the properties and interactions of complex carbohydrates. This may lead to a better understanding of their role in biological systems and the development of new strategies for targeting them in therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 40372-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,7 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40372-09:
(7*4)+(6*0)+(5*3)+(4*7)+(3*2)+(2*0)+(1*9)=86
86 % 10 = 6
So 40372-09-6 is a valid CAS Registry Number.
40372-09-6Relevant articles and documents
Loss of individual electrostatic interactions between aminoglycoside antibiotics and resistance enzymes as an effective means to overcoming bacterial drug resistance
Roestamadji, Juliatiek,Grapsas, Ioannis,Mobashery, Shahriar
, p. 11060 - 11069 (1995)
Aminoglycoside-modifying enzymes modify the structures of aminoglycoside antibiotics, rendering them ineffective, a process which confers resistance to the antibiotic. Electrostatic interactions (ion pairing and hydrogen bonding) are believed to be signif
