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1,3-bis(3,4-dimethoxyphenyl)propane-1-one, also known as bisdemethoxycurcumin, is a synthetic organic compound derived from curcumin, a natural phenolic compound found in the spice turmeric. It is characterized by its molecular structure, which consists of two 3,4-dimethoxyphenyl groups attached to a propane-1-one backbone. 1,3-bis(3,4-dimethoxyphenyl)propane-1-one exhibits enhanced stability and bioavailability compared to curcumin, making it a promising candidate for pharmaceutical applications, particularly in the treatment of various diseases, such as cancer, inflammation, and neurodegenerative disorders. The presence of methoxy groups on the phenyl rings increases the lipophilicity of the molecule, facilitating its absorption and distribution within the body. Research on bisdemethoxycurcumin is ongoing to further explore its potential therapeutic effects and optimize its use in clinical settings.

4087-62-1

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4087-62-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4087-62-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,8 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4087-62:
(6*4)+(5*0)+(4*8)+(3*7)+(2*6)+(1*2)=91
91 % 10 = 1
So 4087-62-1 is a valid CAS Registry Number.

4087-62-1Relevant academic research and scientific papers

Structural optimization of natural product nordihydroguaretic acid to discover novel analogues as AcrB inhibitors

Alenzy, Rawaf,Liu, Xingbang,Ma, Shutao,Ma, Yingang,Mowla, Rumana,Polyak, Steven W.,Song, Di,Teng, Yuetai,Venter, Henrietta,Wang, Yinhu

, (2019/12/24)

Drug efflux pumps confer multidrug resistance to dangerous bacterial pathogens which makes these proteins promising drug targets. Herein, we present initial chemical optimization and structure-activity relationship (SAR) data around a previously described efflux pump inhibitor, nordihydroguaretic acid (NDGA). Four series of novel NDGA analogues that target Escherichia coli AcrB were designed, synthesized and evaluated for their ability to potentiate the activity of antibiotics, to inhibit AcrB-mediated substrate efflux and reduce off-target activity. Nine novel structures were identified that increased the efficacy of a panel of antibiotics, inhibited drug efflux and reduced permeabilization of the bacterial outer and inner membranes. Among them, WA7, WB11 and WD6 possessing broad-spectrum antimicrobial sensitization activity were identified as NDGA analogues with favorable properties as potential AcrB inhibitors, demonstrating moderate improvement in potency as compared to NDGA. In particular, WD6 was the most broadly active analogue improving the activity of all four classes of antibacterials tested.

Dihedral-Angle-Controlled Crossover from Static Hole Delocalization to Dynamic Hopping in Biaryl Cation Radicals

Talipov, Marat R.,Navale, Tushar S.,Hossain, Mohammad M.,Shukla, Ruchi,Ivanov, Maxim V.,Rathore, Rajendra

, p. 266 - 269 (2016/12/30)

In cases of coherent charge-transfer mechanism in biaryl compounds the rates follow a squared cosine trend with varying dihedral angle. Herein we demonstrate using a series of biaryl cation radicals with varying dihedral angles that the hole stabilization

Synthesis and biological evaluation of chalcone, dihydrochalcone, and 1,3-diarylpropane analogs as anti-inflammatory agents

Vijaya Bhaskar Reddy, Mopur,Hung, Hsin-Yi,Kuo, Ping-Chung,Huang, Guan-Jhong,Chan, Yu-Yi,Huang, Shiow-Chyn,Wu, Shwu-Jen,Morris-Natschke, Susan L.,Lee, Kuo-Hsiung,Wu, Tian-Shung

, p. 1547 - 1550 (2017/03/17)

Twenty-one chalcones were prepared via aldol condensation and subsequent reduction of these compound led to the corresponding dihydrochalcone and 1,3-diphenylpropane derivatives. The synthetic products were examined for their effects on NO inhibition in L

Domino Reactions Containing Different Types of Heck Reactions for Selective 3,3- and 1,3-Diarylations of Propenol with Aryl Halides by Triple Catalysis

Zhu, Zhi-Qiang,He, Jian-Shi,Wang, Hai-Jun,Huang, Zhi-Zhen

, p. 9354 - 9359 (2015/09/28)

A new domino Heck-isomerization/Saegusa/Heck reaction of propenol with aryl iodides has been developed for the synthesis of 3,3-diaryl propenals by triple transition-metal catalysis. Moreover, we also developed the domino Heck-isomerization/Heck-type reaction of propenol with aryl iodides for the synthesis of 1,3-diaryl propanones by double transition-metal catalysis and the mediation of secondary amine or triple transition metal catalysis and aminocatalysis.

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