70360-12-2 Usage
Uses
Used in Pharmaceutical Industry:
Sideritiflavone is used as a therapeutic agent for its potential cardiovascular health benefits, as it may help in reducing oxidative stress and modulating the immune response. Its antioxidant properties could contribute to the prevention of cardiovascular diseases.
Used in Antiviral Applications:
In the field of virology, sideritiflavone is used as a potential antiviral agent, with ongoing research to understand its effects on inhibiting viral replication and reducing the severity of viral infections.
Used in Anticancer Applications:
Sideritiflavone is being investigated for its potential as an anticancer agent, with studies exploring its ability to target and inhibit the growth of cancer cells, making it a candidate for further research in oncology.
Used in Nutraceutical Industry:
Given its antioxidant and anti-inflammatory properties, sideritiflavone is used as a nutraceutical ingredient to support overall health and well-being, potentially contributing to the prevention of various diseases associated with oxidative stress and inflammation.
Check Digit Verification of cas no
The CAS Registry Mumber 70360-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,3,6 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70360-12:
(7*7)+(6*0)+(5*3)+(4*6)+(3*0)+(2*1)+(1*2)=92
92 % 10 = 2
So 70360-12-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H16O8/c1-23-16-14(22)13-11(21)7-12(8-4-5-9(19)10(20)6-8)26-15(13)17(24-2)18(16)25-3/h4-7,19-20,22H,1-3H3
70360-12-2Relevant academic research and scientific papers
Hydroxylated polymethoxylated flavone and preparation method thereof
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Paragraph 0052-0057, (2021/05/26)
The invention provides hydroxylated polymethoxylated flavone and a preparation method thereof. The chemical structure of a compound is shown as a formula (I). The method comprises the following steps: synthesizing an intermediate product 2a by using an in
Synthesis of 5,3',4'-Trihydroxy-6,7,8-trimethoxyflavone
Bhardwaj, D. K.,Gupta, A. K.,Jain, R. K.
, p. 800 - 801 (2007/10/02)
The structure of a new trihydroxytrimethoxyflavone, isolated from Sideritis leucantha, as 5,3',4'-trihydroxy-6,7,8-trimethoxyflavone (I) has now been confirmed by its synthesis. 2-(3',4'-Dibenzyloxy)benzoyloxy-3,4,5,6-tetramethoxyacetophenone (VI) on Bake
