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Phosphoric acid, (2S)-3-(octylamino)-3-oxo-2-[(1-oxooctyl)amino]propyl bis(phenylmethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

876348-41-3

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876348-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 876348-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,3,4 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 876348-41:
(8*8)+(7*7)+(6*6)+(5*3)+(4*4)+(3*8)+(2*4)+(1*1)=213
213 % 10 = 3
So 876348-41-3 is a valid CAS Registry Number.

876348-41-3Downstream Products

876348-41-3Relevant academic research and scientific papers

Synthesis and pharmacological evaluation of second-generation phosphatidic acid derivatives as lysophosphatidic acid receptor ligands

Durgam, Gangadhar G.,Tsukahara, Ryoko,Makarova, Natalia,Walker, Michelle D.,Fujiwara, Yuko,Pigg, Kathryn R.,Baker, Daniel L.,Sardar, Vineet M.,Parrill, Abby L.,Tigyi, Gabor,Miller, Duane D.

, p. 633 - 640 (2007/10/03)

Short-chain phosphatidic acid derivatives, dioctanoyl glycerol pyrophosphate (DGPP 8:0, 1) and phosphatidic acid 8:0 (PA 8:0, 2), were previously identified as subtype-selective LPA1 and LPA3 receptor antagonists. Recently, we report

Acetal phosphate-derived LPA mimics, PPARgamma activators, and autotaxin inhibitors

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Page/Page column 7; sheet 7, (2010/11/24)

Disclosed are compositions that modulate the effects of extracellular LPA receptors, the intracellular PPARγ receptor, and autotaxin, and methods for their use.

Synthesis and biological evaluation of novel cytotoxic phospholipids for prostate cancer

Gududuru, Veeresa,Hurh, Eunju,Durgam, Gangadhar G.,Hong, Seoung Soo,Sardar, Vineet M.,Xu, Huiping,Dalton, James T.,Miller, Duane D.

, p. 4919 - 4923 (2007/10/03)

A series of serine amide phosphates (SAPs) and serine amide alcohols (SAAs) were prepared and evaluated for their in vitro cytotoxicity against five human prostate cancer cell lines. The SAR and biological activity of the synthesized compounds is reported

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