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(RS)-2-(2,6-dimethylphenoxy)propan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26583-69-7

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26583-69-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26583-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,8 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 26583-69:
(7*2)+(6*6)+(5*5)+(4*8)+(3*3)+(2*6)+(1*9)=137
137 % 10 = 7
So 26583-69-7 is a valid CAS Registry Number.

26583-69-7Relevant academic research and scientific papers

X-ray crystal structures of Enterococcus faecalis thymidylate synthase with folate binding site inhibitors

Catalano, Alessia,Luciani, Rosaria,Carocci, Alessia,Cortesi, Debora,Pozzi, Cecilia,Borsari, Chiara,Ferrari, Stefania,Mangani, Stefano

, p. 649 - 664 (2016)

Infections caused by Enterococcus faecalis (Ef) represent nowadays a relevant health problem. We selected Thymidylate synthase (TS) from this organism as a potential specific target for antibacterial therapy. We have previously demonstrated that species-specific inhibition of the protein can be achieved despite the relatively high structural similarity among bacterial TSs and human TS. We had previously obtained the EfTS crystal structure of the protein in complex with the metabolite 5-formyl-tetrahydrofolate (5-FTHF) suggesting the protein role as metabolite reservoir; however, protein–inhibitors complexes were still missing. In the present work we identified some inhibitors bearing the phthalimidic core from our in-house library and we performed crystallographic screening towards EfTS. We obtained two X-ray crystallographic structures: the first with a weak phthalimidic inhibitor bound in one subunit and 5-hydroxymethylene-6-hydrofolic acid (5-HMHF) in the other subunit; a second X-ray structure complex with methotrexate. The structural information achieved confirm the role of EfTS as an enzyme involved in the folate pool system and provide a structural basis for structure-based drug design.

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