7608-44-8 Usage
Description
Artocarpin is a trihydroxyflavone that is characterized by the presence of hydroxy groups at positions 5, 2', and 4', a methoxy group at position 7, a prenyl group at position 3, and a (1E)-3-methylbut-1-enyl group at position 6. It is isolated from Artocarpus heterophyllus and Artocarpus integrifolia and has been found to exhibit antineoplastic activity.
Uses
Used in Pharmaceutical Industry:
Artocarpin is used as an antineoplastic agent for its potential cancer-fighting properties. It is being studied for its ability to target and inhibit the growth of cancer cells, making it a promising candidate for the development of new cancer treatments.
Used in Drug Discovery and Development:
Artocarpin is used as a lead compound in drug discovery and development efforts. Its unique chemical structure and biological activity make it a valuable starting point for the design and synthesis of new drugs targeting various diseases, including cancer.
Used in Cancer Research:
Artocarpin is used as a research tool in cancer research to better understand the molecular mechanisms underlying its antineoplastic activity. This knowledge can help researchers identify new therapeutic targets and develop more effective cancer treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 7608-44-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,0 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7608-44:
(6*7)+(5*6)+(4*0)+(3*8)+(2*4)+(1*4)=108
108 % 10 = 8
So 7608-44-8 is a valid CAS Registry Number.
7608-44-8Relevant articles and documents
Total syntheses of norartocarpin and artocarpin
Zhang, Wen-Jing,Wu, Jing-Fang,Zhou, Peng-Fei,Wang, Yang,Hou, Ai-Jun
, p. 5850 - 5858 (2013/07/27)
The total syntheses of norartocarpin and artocarpin, two biologically interesting natural flavonoids with two regioisomeric isoprenyl side chains, were achieved for the first time via a linear reaction sequence of 9 and 12 steps with the overall yields of