91411-76-6 Usage
Chemical structure
A complex chemical compound consisting of multiple functional groups and elements, including a phenylpropanoyl group, a phenoxy group, a propylamino group, and a beta-D-glucopyranosiduronic acid group.
Hydrophobic and hydrophilic properties
Likely to have both hydrophobic and hydrophilic properties due to the presence of multiple functional groups.
Potential applications
May have potential applications in medicinal and pharmaceutical fields, possibly as an active ingredient in drug formulations.
Biological activity
The beta-D-glucopyranosiduronic acid moiety indicates that it may have some carbohydrate-related biological activity.
Further research
Further research and analysis would be needed to fully understand its properties and potential uses.
Molecular weight
Approximately 561.65 g/mol
Stereochemistry
The presence of a beta-D-glucopyranosiduronic acid group suggests that the compound has a specific stereochemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 91411-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,4,1 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91411-76:
(7*9)+(6*1)+(5*4)+(4*1)+(3*1)+(2*7)+(1*6)=116
116 % 10 = 6
So 91411-76-6 is a valid CAS Registry Number.
91411-76-6Relevant articles and documents
Synthesis of glucuronides of propafenone and 5-hydroxypropafenone by sepharose-bound uridine 5'-diphosphoglucuronyltransferase
Neidlein,Wu,Hege
, p. 1257 - 1262 (2007/10/02)
Propafenone (Rytmonorm) and its in vivo metabolite 5-hydroxypropafenone were glucuronidated by agarose-bound uridine 5'-diphospho (UDP)-glucuronyltransferase from bovine liver in the presence of UDP-glucuronic acid. The identification of the synthesized glucuronides was based on the specific enzymatic hydrolysis, by mass spectrometry and by chromatographic comparison with isolated metabolites from dog and man. The glucuronidation of propafenone and 5-hydroxypropafenone followed by Michaelis-Menten kinetics up to substrate concentration of 0.4 mmol/l (propafenone) and 0.3 mmol/l (5-hydroxypropafenone). The pH optima were 7.5 and 8.0 respectively. The reaction was linear up to 30 min and for a protein concentration between 1 and 5 mg per assay. 5-Hydroxypropafenone showed the best affinity with a K(m) value of 1.4 mmol/l, in contrast to 11.6 mmol/l for propafenone. The use of agarose-bound UDP-glucuronyltransferase offers the possibility to synthesize propafenone glucuronide and 5-hydroxypropafenone glucuronide which are needed for kinetic and pharmacological studies in man and animals.
