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956380-79-3

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956380-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 956380-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,3,8 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 956380-79:
(8*9)+(7*5)+(6*6)+(5*3)+(4*8)+(3*0)+(2*7)+(1*9)=213
213 % 10 = 3
So 956380-79-3 is a valid CAS Registry Number.

956380-79-3Upstream product

956380-79-3Downstream Products

956380-79-3Relevant academic research and scientific papers

Effects of 3-(4′-geranyloxy-3′-methoxyphenyl)-2-trans propenoic acid and its ester derivatives on biofilm formation by two oral pathogens, Porphyromonas gingivalis and Streptococcus mutans

Bodet, Charles,Epifano, Francesco,Genovese, Salvatore,Curini, Massimo,Grenier, Daniel

, p. 1612 - 1620 (2008)

The aim of this study was to investigate the effect of 3-(4′-geranyloxy-3′-methoxyphenyl)-2-trans propenoic acid, active principle isolated from Acronychia baueri Schott, and its ester derivatives on biofilm formation by two important oral pathogens, Porphyromonas gingivalis and Streptococcus mutans. The parent acid and conjugates with vanillic acid, 2-hydroxynaphthoquinone and guaiacol caused a significant and reproducible inhibition of P. gingivalis biofilm formation. This effect could be related to the ability of the compounds to inhibit bacterial growth. These compounds also efficiently caused a reduction of biofilm formation by S. mutans, a phenomenon not related to growth inhibition. These data suggest that 3-(4′-geranyloxy-3′-methoxyphenyl)-2-trans propenoic acid and some of its ester derivatives may have a therapeutic/preventive potential for oral infections.

Synthesis and anti-inflammatory activity of 3-(4′-geranyloxy-3′-methoxyphenyl)-2-trans propenoic acid and its ester derivatives

Epifano, Francesco,Genovese, Salvatore,Sosa, Silvio,Tubaro, Aurelia,Curini, Massimo

, p. 5709 - 5714 (2008/09/16)

Different esters of 3-(4′-geranyloxy-3′-methoxyphenyl)-2-trans propenoic acid (1), an anti-inflammatory principle of Acronychia baueri Schott (Rutaceae), were synthesized. Their topical anti-inflammatory activity was evaluated using the Croton oil ear tes

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