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3-((2S)-3-(4-(decahydronaphthalen-2-yloxy)phenyl)-2-((4,5-dimethoxy-2-nitrobenzyloxy)carbonylamino)propanamido)propanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1393827-65-0

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1393827-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1393827-65-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,8,2 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1393827-65:
(9*1)+(8*3)+(7*9)+(6*3)+(5*8)+(4*2)+(3*7)+(2*6)+(1*5)=200
200 % 10 = 0
So 1393827-65-0 is a valid CAS Registry Number.

1393827-65-0Downstream Products

1393827-65-0Relevant academic research and scientific papers

Discovery of small-molecule interleukin-2 inhibitors from a DNA-encoded chemical library

Leimbacher, Markus,Zhang, Yixin,Mannocci, Luca,Stravs, Michael,Geppert, Tim,Scheuermann, Jcrg,Schneider, Gisbert,Neri, Dario

, p. 7729 - 7737 (2012/09/07)

Libraries of chemical compounds individually coupled to encoding DNA tags (DNA-encoded chemical libraries) hold promise to facilitate exceptionally efficient ligand discovery. We constructed a high-quality DNAencoded chemical library comprising 30 000 drug-like compounds; this was screened in 170 different affinity capture experiments. High-throughput sequencing allowed the evaluation of 120 million DNA codes for a systematic analysis of selection strategies and statistically robust identification of binding molecules. Selections performed against the tumor-associated antigen carbonic anhydrase IX (CA IX) and the pro-inflammatory cytokine interleukin-2 (IL-2) yielded potent inhibitors with exquisite target specificity. The binding mode of the revealed pharmacophore against IL-2 was confirmed by molecular docking. Our findings suggest that DNA-encoded chemical libraries allow the facile identification of drug-like ligands principally to any protein of choice, including molecules capable of disrupting high-affinity protein-protein interactions.

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