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Decanamide, N-[(1R,2R,3E)-2-hydroxy-1-(hydroxymethyl)-3-heptadecenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

215584-99-9

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215584-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 215584-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,5,8 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 215584-99:
(8*2)+(7*1)+(6*5)+(5*5)+(4*8)+(3*4)+(2*9)+(1*9)=149
149 % 10 = 9
So 215584-99-9 is a valid CAS Registry Number.

215584-99-9Downstream Products

215584-99-9Relevant academic research and scientific papers

Inhibitory activity of a ceramide library on interleukin-4 production from activated T cells

Park, Jin,Li, Qian,Chang, Young-Tae,Kim, Tae Sung

, p. 2589 - 2595 (2005)

Allergic diseases are hypersensitivity disorders associated with the production of specific immunoglobulin E (IgE) to environmental allergens. Interleukin (IL)-4, produced primarily by CD4+ T cells, is an important stimulus for the switch of th

Chiral combinatorial preparation and biological evaluation of unique ceramides for inhibition of sphingomyelin synthase

Koolath, Sajeer,Monde, Kenji,Murai, Yuta,Suga, Yoshiko

supporting information, (2020/02/04)

Enantiomers or diastereomers of chiral bioactive compounds often exhibit different biological and toxicological properties. Here, we report the efficient synthesis of four stereoisomers of sphingosine and derivatization of unique chiral ceramides through a combinatorial chemistry by solid-phase activated resin ester. In addition, to test the effectivity of stereochemistry of ceramide, we demonstrated a cell-based assay of sphingomyelin synthase inhibition in the presence ofchiral unique ceramides, which suggested that libraries of this sort will be a rich source of biologically active synthetic molecules.

The synthesis and biological characterization of a ceramide library

Chang, Young-Tae,Choi, Jaehwa,Ding, Sheng,Prieschl, Eva E.,Baumruker, Thomas,Lee, Jae-Mok,Chung, Sung-Kee,Schultz, Peter G.

, p. 1856 - 1857 (2007/10/03)

A facile synthesis of a combinatorial ceramide library and their activities in the NF-κB pathway and in apoptosis induction/prevention were demonstrated. A novel NF-κB activating molecule was discovered among ceramide containing β-galactose, and the structural requirements of ceramides for apoptosis induction was elucidated. Copyright

Synthesis and evaluation of morpholino- and pyrrolidinosphingolipids as inhibitors of glucosylceramide synthase

Miura, Tsuyoshi,Kajimoto, Tetsuya,Jimbo, Masayuki,Yamagishi, Kiwamu,Inokuchi, Jin-Chi,Wong, Chi-Huey

, p. 1481 - 1489 (2007/10/03)

This paper describes the new synthesis and evaluation of some morpholino- and pyrrolidinosphingolipids and mimics as inhibitors of glucosylceramide synthase. It was found that the pyrrolidino derivatives are generally more active than the morpholino derivatives and the best one was shown to be a nanomolar inhibitor. Copyright (C) 1998 Elsevier Science Ltd.

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