76386-25-9 Usage
Description
[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl] N,N-diphenylcarbamate, also known as squalene epoxidase inhibitor, is a chemical compound that plays a crucial role in inhibiting the activity of squalene epoxidase, a key enzyme involved in the cholesterol biosynthesis pathway. [(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl] N,N-diphenylcarbamate is characterized by its ability to modulate squalene epoxidase activity, making it a valuable asset in pharmaceutical and research applications.
Uses
Used in Pharmaceutical Research:
[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl] N,N-diphenylcarbamate is used as a research tool for studying the role of squalene epoxidase in cholesterol metabolism. Its ability to inhibit this enzyme makes it a potential target for therapeutic intervention in conditions such as hypercholesterolemia, where the regulation of cholesterol levels is essential.
Used in Cancer Treatment Research:
In the field of oncology, [(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl] N,N-diphenylcarbamate is being investigated for its potential use in the treatment of cancer. Its mechanism of action in inhibiting squalene epoxidase may offer new avenues for cancer therapy, as the enzyme's activity has been linked to cancer cell growth and survival.
Used in Antifungal Agent Development:
Additionally, [(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl] N,N-diphenylcarbamate is being explored for its potential as an antifungal agent. The inhibition of squalene epoxidase by this compound could provide a novel approach to combating fungal infections, which are a significant concern in both medical and agricultural settings.
Overall, [(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl] N,N-diphenylcarbamate has a wide range of applications in the pharmaceutical and research industries, primarily due to its ability to modulate squalene epoxidase activity. Its potential use in treating hypercholesterolemia, cancer, and fungal infections highlights its versatility and importance in the development of new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 76386-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,8 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76386-25:
(7*7)+(6*6)+(5*3)+(4*8)+(3*6)+(2*2)+(1*5)=159
159 % 10 = 9
So 76386-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C28H35NO2/c1-23(2)13-11-14-24(3)15-12-16-25(4)21-22-31-28(30)29(26-17-7-5-8-18-26)27-19-9-6-10-20-27/h5-10,13,15,17-21H,11-12,14,16,22H2,1-4H3/b24-15+,25-21+
