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20958-17-2

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20958-17-2 Usage

General Description

4,8-Dimethylphenanthro[3,2-b]furan-7,11-dione is a chemical compound with a complex molecular structure. It belongs to the group of phenanthrenes, which are polycyclic aromatic hydrocarbons. 4,8-Dimethylphenanthro[3,2-b]furan-7,11-dione is characterized by the presence of a furan ring and two methyl groups, located at positions 4 and 8 on the phenanthrene backbone. It is a yellow crystalline solid with potential applications in the field of organic synthesis and medicinal chemistry. The compound's unique structure and potential reactivity make it an interesting target for further research and exploration.

Check Digit Verification of cas no

The CAS Registry Mumber 20958-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,9,5 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20958-17:
(7*2)+(6*0)+(5*9)+(4*5)+(3*8)+(2*1)+(1*7)=112
112 % 10 = 2
So 20958-17-2 is a valid CAS Registry Number.

20958-17-2Downstream Products

20958-17-2Relevant articles and documents

Evaluation of the anti-inflammatory effects of synthesised tanshinone I and isotanshinone I analogues in zebrafish

Foulkes, Matthew J.,Tolliday, Faith H.,Henry, Katherine M.,Renshaw, Stephen A.,Jones, Simon

, (2020/10/20)

During inflammation, dysregulated neutrophil behaviour can play a major role in a range of chronic inflammatory diseases, for many of which current treatments are generally ineffective. Recently, specific naturally occurring tanshinones have shown promising anti-inflammatory effects by targeting neutrophils in vivo, yet such tanshinones, and moreover, their isomeric isotanshinone counterparts, are still a largely underexplored class of compounds, both in terms of synthesis and biological effects. To explore the anti-inflammatory effects of isotanshinones, and the tanshinones more generally, a series of substituted tanshinone and isotanshinone analogues was synthesised, alongside other structurally similar molecules. Evaluation of these using a transgenic zebrafish model of neutrophilic inflammation revealed differential anti-inflammatory profiles in vivo, with a number of compounds exhibiting promising effects. Several compounds reduce initial neutrophil recruitment and/or promote resolution of neutrophilic inflammation, of which two also result in increased apoptosis of human neutrophils. In particular, the methoxy-substituted tanshinone 39 specifically accelerates resolution of inflammation without affecting the recruitment of neutrophils to inflammatory sites, making this a particularly attractive candidate for potential pro-resolution therapeutics, as well as a possible lead for future development of functionalised tanshinones as molecular tools and/or chemical probes. The structurally related β-lapachones promote neutrophil recruitment but do not affect resolution. We also observed notable differences in toxicity profiles between compound classes. Overall, we provide new insights into the in vivo anti-inflammatory activities of several novel tanshinones, isotanshinones, and structurally related compounds.

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