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2H-Indol-2-one, 1-(2,6-dichloro-3-methylphenyl)-1,3-dihydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15310-40-4

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15310-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15310-40-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,1 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15310-40:
(7*1)+(6*5)+(5*3)+(4*1)+(3*0)+(2*4)+(1*0)=64
64 % 10 = 4
So 15310-40-4 is a valid CAS Registry Number.

15310-40-4Relevant academic research and scientific papers

Albumin-binding compounds that prevent nonenzymatic glycation and that may be used for treatment of glycation-related pathologies

-

, (2008/06/13)

The present invention is directed to compositions that inhibit the nonenzymatic glycation of albumin,, as well as methods of using compounds that inhibit albumin glycation for the treatment of glycation-related pathologies.

Synthesis and quantitative structure-activity relationships of diclofenac analogues

Moser,Sallmann,Wiesenberg

, p. 2358 - 2368 (2007/10/02)

The synthesis of a series of 2-anilinophenylacetic acid, close analogues of diclofenac, is described. These compounds were tested in two models used for evaluating the activity of nonsteroidal antiinflammatory drugs (NSAID's), inhibition of cyclooxygenase enzyme activity in vitro, and adjuvant-induced arthritis (AdA) in rats. Statistically significant correlations were found between the inhibitory activities of the compounds in these two models, indicating that cyclooxygenase inhibition seems to be the underlying mechanism for the antiinflammatory activity of these compounds. Quantitative structure-activity relationship (QSAR) analysis revealed that the crucial parameters for activity in both models were the lipophilicity and the angle of twist between the two phenyl rings. Optimal activities were associated with halogen or alkyl substituents in both ortho positions of the anilino ring. Compounds with OH groups in addition to two ortho substituents or compounds with only one or no ortho substituents were less active.

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