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7,8-Dihydroxy-4'-methoxy isoflavone (Retusin) is a naturally occurring chemical compound belonging to the isoflavone class, found in plants such as soybeans, chickpeas, and other legumes. It is recognized for its potential antioxidant and anti-inflammatory properties and has been studied for its therapeutic effects on various health conditions.

37816-19-6

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37816-19-6 Usage

Uses

Used in Pharmaceutical Applications:
7,8-Dihydroxy-4'-methoxy isoflavone (Retusin) is used as a therapeutic agent for its potential health benefits in treating conditions such as cancer, osteoporosis, and menopausal symptoms. Its antioxidant and anti-inflammatory properties contribute to its potential efficacy in these areas.
Used in Cardiovascular Health Applications:
In the field of cardiovascular health, 7,8-Dihydroxy-4'-methoxy isoflavone (Retusin) is used for its potential benefits in promoting heart health, although the specific mechanisms and applications are still under investigation.
Used in Skin Health Applications:
7,8-Dihydroxy-4'-methoxy isoflavone (Retusin) is utilized in skin health applications due to its potential to improve skin conditions and promote overall skin wellness, likely due to its antioxidant properties.
Used in Nutraceutical Applications:
Retusin is also used in the development of nutraceutical products, capitalizing on its potential health benefits to support overall well-being and address specific health concerns.
Further research is necessary to fully understand the mechanisms of action and potential therapeutic applications of 7,8-Dihydroxy-4'-methoxy isoflavone (Retusin) in these industries.

Check Digit Verification of cas no

The CAS Registry Mumber 37816-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,8,1 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37816-19:
(7*3)+(6*7)+(5*8)+(4*1)+(3*6)+(2*1)+(1*9)=136
136 % 10 = 6
So 37816-19-6 is a valid CAS Registry Number.

37816-19-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7,8-dihydroxy-3-(4-methoxyphenyl)chromen-4-one

1.2 Other means of identification

Product number -
Other names Retusin(Dalbergia)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:37816-19-6 SDS

37816-19-6Relevant academic research and scientific papers

Natural Isoflavones and Semisynthetic Derivatives as Pancreatic Lipase Inhibitors

Cardullo, Nunzio,Muccilli, Vera,Pulvirenti, Luana,Tringali, Corrado

, p. 654 - 665 (2021/04/02)

Obesity, now widespread all over the world, is frequently associated with some chronic diseases. Thus, there is a growing interest in the prevention and treatment of obesity. To date, the only antiobesity drug is orlistat, a natural product-derived pancreatic lipase (PL) inhibitor with some undesired side effects. In the last decades, many natural compounds or derivatives have been evaluated as potential PL inhibitors, and natural polyphenols are among the most promising for possible exploitation as antiobesity agents. However, few studies have been devoted to isoflavones. In this work, we report a study on the PL inhibitory properties of a small library of semisynthetic isoflavone derivatives together with the natural leads daidzein (1), genistein (2), and formononetin (3). In vitro lipase inhibition assay showed that 2 is the most promising PL inhibitor. Among synthetic isoflavones, the hydroxylated and brominated derivatives were more potent than their natural leads. Detailed studies through fluorescence measurements and kinetics of lipase inhibition showed that 2 and the bromoderivatives 10 and 11 have the greatest affinity for PL. Docking studies corroborated these findings highlighting the interactions between isoflavones and the enzyme, confirming that hydroxylation and bromination are useful modifications.

Free-radical-scavenging, antityrosinase, and cellular melanogenesis inhibitory activities of synthetic isoflavones

Lu, Tzy-Ming,Ko, Horng-Huey,Ng, Lean-Teik,Hsieh, Yen-Pin

, p. 963 - 979 (2015/06/25)

In this study, we examined the potential of synthetic isoflavones for application in cosmeceuticals. Twenty-five isoflavones were synthesized and their capacities of free-radical-scavenging and mushroom tyrosinase inhibition, as well as their impact on cell viability of B16F10 murine melanoma cells and HaCaT human keratinocytes were evaluated. Isoflavones that showed significant mushroom tyrosinase inhibitory activities were further studied on reduction of cellular melanin formation and antityrosinase activities in B16F10 melanocytes in vitro. Among the isoflavones tested, 6-hydroxydaidzein (2) was the strongest scavenger of both ABTS.+ and DPPH. radicals with SC50 values of 11.3±0.3 and 9.4±0.1 μM, respectively. Texasin (20) exhibited the most potent inhibition of mushroom tyrosinase (IC50 14.9±4.5 μM), whereas retusin (17) showed the most efficient inhibition both of cellular melanin formation and antityrosinase activity in B16F10 melanocytes, respectively. In summary, both retusin (17) and texasin (20) exhibited potent free-radical-scavenging capacities as well as efficient inhibition of cellular melanogenesis, suggesting that they are valuable hit compounds with potential for advanced cosmeceutical development.

A mild and efficient protocol to synthesize chromones, isoflavones, and homoisoflavones using the complex 2,4,6-trichloro-1,3,5-triazine/ dimethylformamide

Basha, G. Mahaboob,Yadav, S. Kumar,Srinuvasarao,Prasanthi,Ramu,Mangarao,Siddaiah

, p. 763 - 768 (2013/08/23)

A mild and efficient one-flask method has been developed for the synthesis of chromones, isoflavones, and homoisoflavones from 2-hydroxyacetophenones, deoxybenzoins, and dihydrochalcones, respectively, via one-carbon extension using the complex 2,4,6-trichloro-1,3,5-triazine/dimethylformamide. Deoxybenzoins and dihydrochalcones were prepared in situ by the reaction of readily available substituted phenols with phenylacetic acids and 3-phenylpropanoic acids, respectively. This method allows the synthesis of a wide range of compounds with multiple phenolic hydroxyls and other substituents. The methodology has been applied to the synthesis of three naturally occurring isoflavones such as formononetin (9c), daidzein (9d), and retusin (9h).

Synthesis of various kinds of isoflavones, isoflavanes, and biphenyl- ketones and their 1,1-diphenyl-2-picrylhydrazyl radical-scavenging activities

Goto, Hideyuki,Terao, Yoshiyasu,Akai, Shuji

experimental part, p. 346 - 360 (2009/12/27)

Forty-eight kinds of isoflavones (8), thirty-one isoflavanes (9), and forty-seven biphenyl-ketones (10, 10') were synthesized from eleven kinds of substituted phenols (11) and six phenylacetic acids (12). Among them, seventy-five compounds are new. The radical scavenging activities of these compounds were evaluated using 1,1- diphenyl-2-picrylhydrazyl (DPPH) at pH 6.0. We found that thirty-nine out of forty-three compounds having a catechol moiety on either the A- or the B-ring exhibited a high activity (ED50=12-54 μM) similar to that of catechin. In these cases, the remaining part of their structure seemed to have little effect on their activity. Many 6- or 8-hydroxyisoflavanes (9E-I) and their biphenyl-ketone derivatives (10E-H) also showed a high activity (ED50=50=26-32 μM). This study suggests that natural isoflavones have the possibilities of exhibiting antioxidant activities through the hydroxylation at the C6-, C8-, or C3'-position or the formation of the isoflavanes (9) and/or the biphenyl-ketone derivatives (10') by metabolism or biotransformation.

Inhibition of extrahepatic human cytochromes P450 1A1 and 1B1 by metabolism of isoflavones found in Trifolium pratense (red clover)

Roberts, Dean W.,Doerge, Daniel R.,Churchwell, Mona I.,Da Costa, Goncalo Gamboa,Marques, M. Matilde,Tolleson, William H.

, p. 6623 - 6632 (2007/10/03)

Biochanin A and formononetin are the predominant isoflavones in red clover. In a previous study (J. Agric. Food Chem. 2002, 50, 4783-4790), it was demonstrated that human liver microsomes converted biochanin A and formononetin to genistein and daidzein. This paper now shows CYP1B1-catalyzed O-demethylation of biochanin A and formononetin to produce genistein and daidzein, respectively, which inhibit CYP1B1. Recombinant human CYP1A1 or CYP1B1 was incubated with biochanin A or formononetin. CYP1A1 catalyzed isoflavone 4′-O-demethylation and hydroxylations with similar efficiency, whereas CYP1B1 favored 4′-O-demethylation over hydroxylations. Three of the biochanin A metabolites (5,7,3′-trihydroxy-4′-methoxyisoflavone, 5,7,8-trihydroxy-4′-methoxyisoflavone, and 5,6,7-trihydroxy-4′- methoxyisoflavone) were characterized by 1H NMR spectroscopy and mass spectrometry. Daidzein (Ki = 3.7 μM) exhibited competitive inhibition of CYP1B1 7-ethoxyresorufin O-deethylase activity, and genistein (Ki = 1.9 μM) exhibited mixed inhibition. Biochanin A and/or formononetin may exert anticarcinogenic effects directly by acting as competitive substrates for CYP1B1 or indirectly through their metabolites daidzein and genistein, which inhibit CYP1B1.

The preparation of new isoflavones

Sepulveda-Boza,Walizei,Rezende,Vasquez,Mascayano,Mejias

, p. 1933 - 1940 (2007/10/03)

The synthesis of ten new isoflavones in good yield is described. The method, involving intermediate 2-hydroxybenzyl ketones, did not require protection of the hydroxyl groups of the starting polyphenols.

Synthesis of Isoflavone-H, Occuring in Tephrosia maxima

Parmar, V. S.,Singh, Suddham,Jain, Rajni

, p. 166 - 167 (2007/10/02)

7,8-Methylenedioxy-4'-methoxyisoflavone (I), a new isoflavone reported to occur in the aerial parts and roots of Tephrosia maxima has been synthesized by two methods: (i) by rearrangement of 2'-hydroxy-3',4'-methylenedioxy-4-methoxychalcone (III) with tha

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