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(2R)-2-Octanoylamino-2-phenylethylphosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

289049-75-8

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289049-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 289049-75-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,9,0,4 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 289049-75:
(8*2)+(7*8)+(6*9)+(5*0)+(4*4)+(3*9)+(2*7)+(1*5)=188
188 % 10 = 8
So 289049-75-8 is a valid CAS Registry Number.

289049-75-8Downstream Products

289049-75-8Relevant 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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