6289-72-1 Usage
Description
(5E)-1-(1,3-benzodioxol-5-yl)-5-[1-(2-chlorobenzyl)-1H-indol-3-yl]methylidenepyrimidine-2,4,6(1H,3H,5H)-trione is a heterocyclic organic compound characterized by the presence of a pyrimidine ring and an indole ring connected by an imine group, with an additional benzodioxol moiety attached to the pyrimidine ring. This complex molecular structure endows the compound with a range of biological activities, making it a promising candidate for pharmaceutical development.
Uses
Used in Pharmaceutical Development:
(5E)-1-(1,3-benzodioxol-5-yl)-5-[1-(2-chlorobenzyl)-1H-indol-3-yl]methylidenepyrimidine-2,4,6(1H,3H,5H)-trione is used as a potential drug candidate for its demonstrated biological activities, including anticancer and antimicrobial properties. (5E)-1-(1,3-benzodioxol-5-yl)-5-[1-(2-chlorobenzyl)-1H-indol-3-yl]methylidenepyrimidine-2,4,6(1H,3H,5H)-trione's unique structure allows it to target various biological pathways, offering a versatile platform for the development of new therapeutics to treat a range of diseases.
Used in Anticancer Research:
In the field of oncology, (5E)-1-(1,3-benzodioxol-5-yl)-5-[1-(2-chlorobenzyl)-1H-indol-3-yl]methylidenepyrimidine-2,4,6(1H,3H,5H)-trione is used as an anticancer agent. Its ability to interact with multiple cellular targets makes it a valuable tool in the fight against cancer, as it may help to inhibit tumor growth and proliferation.
Used in Antimicrobial Applications:
(5E)-1-(1,3-benzodioxol-5-yl)-5-[1-(2-chlorobenzyl)-1H-indol-3-yl]methylidenepyrimidine-2,4,6(1H,3H,5H)-trione is also used as an antimicrobial agent, leveraging its biological activities to combat various microbial infections. This application could be particularly useful in the development of new antibiotics to address the growing issue of antibiotic resistance.
Further research is necessary to fully understand the therapeutic potential of (5E)-1-(1,3-benzodioxol-5-yl)-5-[1-(2-chlorobenzyl)-1H-indol-3-yl]methylidenepyrimidine-2,4,6(1H,3H,5H)-trione and to optimize its use in various medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6289-72-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6289-72:
(6*6)+(5*2)+(4*8)+(3*9)+(2*7)+(1*2)=121
121 % 10 = 1
So 6289-72-1 is a valid CAS Registry Number.