71080-05-2 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-methylbutan-2-yl)-2-(2-methylquinolin-4-yl)-1-(1,3-thiazol-2-yl)guanidine is used as a potential pharmaceutical compound for its unique structural features. The presence of guanidine, thiazole, and quinolinyl groups may endow the molecule with specific biological activities, making it a candidate for further research and development in the field of drug discovery and design.
Used in Medicinal Chemistry Research:
In the realm of medicinal chemistry, 1-(2-methylbutan-2-yl)-2-(2-methylquinolin-4-yl)-1-(1,3-thiazol-2-yl)guanidine is used as a subject of study to explore its chemical properties and potential interactions with biological targets. Understanding these interactions can lead to the development of new therapeutic agents.
Used in Drug Design and Development:
1-(2-methylbutan-2-yl)-2-(2-methylquinolin-4-yl)-1-(1,3-thiazol-2-yl)guanidine is utilized in drug design and development efforts due to its unique structural elements, which may allow for the creation of new drugs with novel mechanisms of action. 1-(2-methylbutan-2-yl)-2-(2-methylquinolin-4-yl)-1-(1,3-thiazol-2-yl)guanidine's potential to form hydrogen bonds and its diverse pharmacological activities make it an interesting starting point for the development of new therapeutics.
Check Digit Verification of cas no
The CAS Registry Mumber 71080-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,8 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 71080-05:
(7*7)+(6*1)+(5*0)+(4*8)+(3*0)+(2*0)+(1*5)=92
92 % 10 = 2
So 71080-05-2 is a valid CAS Registry Number.
71080-05-2Relevant academic research and scientific papers
Basic Antiinflammatory Compounds. N,N',N''-Trisubstituted Guanidines
Rachlin, Schneur,Bramm, E.,Ahnfelt-Ronne, I.,Arrigoni-Martelli, E.
, p. 13 - 20 (2007/10/02)
A variety of basic N,N',N''-trisubstituted guanidines was prepared and tested for antiinflammatory activity.Compounds with a thiazoylguanidine moiety linked to the 4 position of the 2-methylquinoline ring exhibited fairly high antiinflammatory activity.Optimal activity was associated with the presence of N-cycloalkyl substituents on N''-4-(2-methylquinolyl)-N'-2-thiazolylguanidine.Pharmalogical data on N-cyclohexyl-N''-4-(2-methylquinolyl)-N'-2-thiazolylguanidine (SR 1368, 44) are presented and discussed.
