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1,5-bis-(4-hydroxy-3-methoxy-phenyl)-pentan-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

47375-84-8

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47375-84-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 47375-84-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,3,7 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 47375-84:
(7*4)+(6*7)+(5*3)+(4*7)+(3*5)+(2*8)+(1*4)=148
148 % 10 = 8
So 47375-84-8 is a valid CAS Registry Number.

47375-84-8Downstream Products

47375-84-8Relevant academic research and scientific papers

Antimicrobial Activity of Monoketone Curcuminoids Against Cariogenic Bacteria

Vieira, Tatiana M.,dos Santos, Isabella A.,Silva, Thayná S.,Martins, Carlos H. G.,Crotti, Ant?nio E. M.

, (2018/08/01)

We evaluated the antimicrobial activity of 25 monoketone curcuminoids (MKCs) against a representative panel of cariogenic bacteria in terms of their minimum inhibitory concentration (MIC) values. Curcumin A (10) displayed promising activity against Streptococcus mutans (MIC?=?50?μg/ml) and Streptococcus mitis (MIC?=?50?μg/ml) as well as moderate activity against S.?sanguinis (MIC?=?100?μg/ml), Lactobacillus casei (MIC?=?100?μg/ml), and Streptococcus salivarius (MIC?=?200?μg/ml). Results indicated higher activity of compound 10 than that of its bis-β-diketone analog. Additionally, compounds 3a (1,5-bis(4-methylphenyl)pentan-3-one) and 7b (1,5-bis(4-bromophenyl)pentan-3-ol) were moderately active against S.?mitis (MIC?=?100?μg/ml) and S.?salivarus (MIC?=?200?μg/ml).

Method and compounds for cancer treatment utilizing NFkB as a direct or ultimate target for small molecule inhibitors

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Page/Page column 4; sheet 2, (2008/06/13)

A method is described for cancer treatment through NFκB inhibition. NFκB is a direct or ultimate target for small molecule inhibitors. These small molecule inhibitors are aimed at suppression of NFκB directly or by indirect suppression of IKK, SFK kinases, or other upstream kinases. The present invention includes small molecule inhibitors comprising three, five, and seven carbon unsaturated spacers having one or two carbonyls, flanked by substituted aryl rings. The small molecule inhibitors can be symmetrical or unsymmetrical.

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