140224-67-5 Usage
Uses
Used in Pharmaceutical Industry:
Trilobacin is used as a cytotoxic agent for its ability to inhibit the growth and proliferation of cancer cells. It has shown potential in targeting various types of cancer cells, making it a valuable compound for further research and development in the field of oncology.
Used in Cancer Research:
Trilobacin is utilized as a research tool for studying the mechanisms of cytotoxicity and cell death in cancer cells. Its use in cancer research can contribute to the understanding of cancer biology and the development of novel therapeutic strategies.
Used in Drug Development:
Trilobacin serves as a starting point for the development of new anticancer drugs. Its cytotoxic properties can be further optimized and modified to improve its efficacy and selectivity towards cancer cells, potentially leading to the creation of more effective cancer treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 140224-67-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,2,2 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 140224-67:
(8*1)+(7*4)+(6*0)+(5*2)+(4*2)+(3*4)+(2*6)+(1*7)=85
85 % 10 = 5
So 140224-67-5 is a valid CAS Registry Number.
InChI:InChI=1/C37H66O7/c1-3-4-5-6-7-11-14-17-20-31(39)33-22-24-35(43-33)36-25-23-34(44-36)32(40)21-18-15-12-9-8-10-13-16-19-30(38)27-29-26-28(2)42-37(29)41/h26,28,30-36,38-40H,3-25,27H2,1-2H3
140224-67-5Relevant academic research and scientific papers
Asymmetric total synthesis of trilobacin via organoselenium-mediated oxonium ion formation/SiO2-Promoted fragmentation
Sohn, Te-Ik,Kim, Mi Jung,Kim, Deukjoon
supporting information; experimental part, p. 12226 - 12227 (2010/10/21)
An asymmetric total synthesis of trilobacin (1), an annonaceous acetogenin with potent anticancer activities, was accomplished wherein the construction of its erythro-bis(2,2′)-tetrahydrofuran core 2 featured a novel organoselenium-mediated oxonium ion formation/SiO2-promoted fragmentation of α,α′-cis-oxocene 3.