50276-96-5 Usage
Uses
Used in Pharmaceutical Industry:
Ochnaflavone is used as a potential therapeutic agent for its ability to inhibit the growth of certain cancer cells, making it a candidate for cancer treatment.
Used in Health Supplements:
Ochnaflavone is used as an antioxidant and anti-inflammatory component in health supplements to support overall health and well-being.
Used in Natural Remedies:
Ochnaflavone is used as a natural remedy for conditions such as inflammation, diabetes, and cardiovascular disease due to its potential health benefits in these areas.
Used in Cosmetics Industry:
Ochnaflavone may be used as an ingredient in cosmetics for its antioxidant properties, potentially contributing to skin health and protection against environmental stressors.
Check Digit Verification of cas no
The CAS Registry Mumber 50276-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,2,7 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50276-96:
(7*5)+(6*0)+(5*2)+(4*7)+(3*6)+(2*9)+(1*6)=115
115 % 10 = 5
So 50276-96-5 is a valid CAS Registry Number.
InChI:InChI=1/C30H18O10/c31-16-8-20(34)29-22(36)12-24(39-27(29)10-16)14-1-4-18(5-2-14)38-26-7-15(3-6-19(26)33)25-13-23(37)30-21(35)9-17(32)11-28(30)40-25/h1-13,31-35H
50276-96-5Relevant academic research and scientific papers
Synthesis of ochnaflavone and its inhibitory activity on PGE2 production
Kim, Sung Soo,Van Vo, Anh,Park, Haeil
, p. 3219 - 3223 (2015/04/22)
Ochnaflavone, a naturally occurring biflavonoid composed of two units of apigenin (5,7,4′-trihydroxyflavone) joined via a C-O-C linkage, was first synthesized and evaluated its inhibitory activity on PGE2 production. Total synthesis was accompl
Total synthesis of ochnaflavone
Ndoile, Monica M.,Van Heerden, Fanie R.
, p. 1346 - 1351 (2013/08/23)
The first total syntheses of ochnaflavone, an asymmetric biflavone consisting of apigenin and luteolin moieties, and the permethyl ether of 2,3,2'',3''-tetrahydroochnaflavone have been achieved. The key steps in the synthesis of ochnaflavone were the formation of a diaryl ether and ring cyclization of an ether-linked dimeric chalcone to assemble the two flavone nuclei. Optimal experimental conditions for the oxidative cyclization to form ochnaflavone were established.
