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dibenzyl 2-(3-ethoxycarbonylmethyloxyphenyl)-2-(octanoylamino)ethyl phosphite is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

532986-70-2

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532986-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 532986-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,2,9,8 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 532986-70:
(8*5)+(7*3)+(6*2)+(5*9)+(4*8)+(3*6)+(2*7)+(1*0)=182
182 % 10 = 2
So 532986-70-2 is a valid CAS Registry Number.

532986-70-2Relevant academic research and scientific papers

Drugs containing phosphoric acid derivatives as the active ingredient

-

, (2008/06/13)

The present invention relates to phosphoric acid derivatives represented by general formula (I), wherein each symbol is as defined in the description and nontoxic salts thereof. Because of having a TNFα production inhibitory effect, the compounds represented by general formula (I) are useful as preventives and/or remedies for rheumatoid arthritis, ulcerative colitis, Crohn's disease, hepatitis, sepsis, hemorrhagic shock, multiple sclerosis, cerebral infarction, diabetes, interstitial pneumonia, uveitis, pain, glomerulonephritis, HIV-associated diseases, cachexia, myocardial infarction, chronic heart failure, oral aphtha, Hansen's disease, infection, etc.

Highly potent inhibitors of TNF-α production. Part I: Discovery of new chemical leads and their structure-activity relationships

Matsui, Toshiaki,Kondo, Takashi,Nishita, Yoshitaka,Itadani, Satoshi,Nakatani, Shingo,Omawari, Nagashige,Sakai, Masaru,Nakazawa, Shuichi,Ogata, Akihito,Mori, Hideaki,Terai, Kouichiro,Kamoshima, Wataru,Ohno, Hiroyuki,Obata, Takaaki,Nakai, Hisao,Toda, Masaaki

, p. 3757 - 3786 (2007/10/03)

Discovery of new chemical leads of inhibitors for TNF-α production starting from the chemical modification of 1 is reported. Further biological studies of 1 to disclose the site of its action strongly suggested that 1 inhibits LPS-induced TNF-α expression

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