181935-41-1 Usage
Uses
Used in Pharmaceutical Applications:
2,4(1H,3H)-Pyrimidinedione, 3-benzoyl-1-[(1S,2S,4S,5R)-4-(1,1-dimethylethoxy)-5-[(phenylmethoxy)methyl]bicyclo[3.1.0]hex-2-yl]-5-methylis used as a potential pharmaceutical compound for its complex structure and possible biological activity. 2,4(1H,3H)-Pyrimidinedione,
3-benzoyl-1-[(1S,2S,4S,5R)-4-(1,1-dimethylethoxy)-5-[(phenylmethoxy)
methyl]bicyclo[3.1.0]hex-2-yl]-5-methyl-'s unique arrangement of functional groups may contribute to its potential therapeutic effects, making it a candidate for further research and development in the pharmaceutical industry.
Used in Drug Development:
In the field of drug development, 2,4(1H,3H)-Pyrimidinedione, 3-benzoyl-1-[(1S,2S,4S,5R)-4-(1,1-dimethylethoxy)-5-[(phenylmethoxy)methyl]bicyclo[3.1.0]hex-2-yl]-5-methylis used as a starting point for the synthesis of new drug compounds. Its complex structure and potential biological activity make it an interesting candidate for further exploration and modification to create novel therapeutic agents.
Used in Research and Testing:
2,4(1H,3H)-Pyrimidinedione, 3-benzoyl-1-[(1S,2S,4S,5R)-4-(1,1-dimethylethoxy)-5-[(phenylmethoxy)methyl]bicyclo[3.1.0]hex-2-yl]-5-methylis used as a research compound in academic and industrial laboratories. Its unique structure and potential biological activity make it a valuable tool for studying various biological processes and mechanisms, as well as for testing its efficacy in different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 181935-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,9,3 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 181935-41:
(8*1)+(7*8)+(6*1)+(5*9)+(4*3)+(3*5)+(2*4)+(1*1)=151
151 % 10 = 1
So 181935-41-1 is a valid CAS Registry Number.
181935-41-1Relevant academic research and scientific papers
Nucleosides with a twist. Can fixed forms of sugar ring pucker influence biological activity in nucleosides and oligonucleotides?
Marquez, Victor E.,Siddiqui, Maqbool A.,Ezzitouni, Abdallah,Russ, Pamela,Wang, Jianying,Wagner, Richard W.,Matteucci, Mark D.
, p. 3739 - 3747 (2007/10/03)
The sugar moiety of nucleosides in solution is known to exist in a rapid dynamic equilibrium between extreme Northern and Southern conformations as defined in the pseudorotational cycle. In the present work, we describe how the bicyclo[3.1.0]hexane templa
