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Acetic acid, [[1-(3,4,5-trimethoxybenzoyl)-2-naphthalenyl]oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

850146-73-5

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850146-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 850146-73-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,1,4 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 850146-73:
(8*8)+(7*5)+(6*0)+(5*1)+(4*4)+(3*6)+(2*7)+(1*3)=155
155 % 10 = 5
So 850146-73-5 is a valid CAS Registry Number.

850146-73-5Downstream Products

850146-73-5Relevant academic research and scientific papers

Synthesis of 1-(3′,4′,5′-trimethoxy) phenyl naphtho[2,1b]furan as a novel anticancer agent

Srivastava, Vandana,Negi, Arvind S.,Kumar,Faridi, Uzma,Sisodia, Brijesh S.,Darokar,Luqman, Suaib,Khanuja

, p. 911 - 914 (2007/10/03)

3′,4′,5′-Trimethoxy benzoyl-naphthalene 2-O-acetic acid (5) underwent base catalysed intramolecular condensation to yield exclusively 1-(3′,4′,5′-trimethoxy) phenyl naphtho[2,1-b]furan 8. The cyclised product 8 has been characterised by spectroscopy. The

Synthesis of gallic acid based naphthophenone fatty acid amides as cathepsin D inhibitors

Srivastava, Vandana,Saxena, Hari Om,Shanker, Karuna,Kumar,Luqman, Suaib,Gupta,Khanuja,Negi, Arvind S.

, p. 4603 - 4608 (2007/10/03)

Gallic acid, one of the most abundant plant phenolic acids, has been modified to cathepsin D protease inhibitors. The strategy of modification was proposed basing on some previously reported structure and activity relationship (SAR) studies. The synthesized naphthophenone fatty acid amide derivatives have been evaluated for in vitro cathepsin D inhibition activity. Two of them have shown significant inhibition activity with IC50 values of 0.06 and 0.14 μM, respectively, as compared against pepstatin (0.0023 μM), the most potent inhibitor known so far. The study revealed that such attempts on gallic acid based pharmacophores might result in potent inhibitors of cathepsin D.

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