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3-ethylsulfanyl-5-phenoxymethyl-4-phenyl-4H-[1,2,4]triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21358-35-0

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21358-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21358-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,5 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21358-35:
(7*2)+(6*1)+(5*3)+(4*5)+(3*8)+(2*3)+(1*5)=90
90 % 10 = 0
So 21358-35-0 is a valid CAS Registry Number.

21358-35-0Downstream Products

21358-35-0Relevant academic research and scientific papers

Alkylsulfanyl-1,2,4-triazoles, a New Class of allosteric valosine containing protein inhibitors. Synthesis and structure-activity relationships

Polucci, Paolo,Magnaghi, Paola,Angiolini, Mauro,Asa, Daniela,Avanzi, Nilla,Badari, Alessandra,Bertrand, Jay,Casale, Elena,Cauteruccio, Silvia,Cirla, Alessandra,Cozzi, Liviana,Galvani, Arturo,Jackson, Peter K.,Liu, Yichin,Magnuson, Steven,Malgesini, Beatrice,Nuvoloni, Stefano,Orrenius, Christian,Sirtori, Federico Riccardi,Riceputi, Laura,Rizzi, Simona,Trucchi, Beatrice,O'Brien, Tom,Isacchi, Antonella,Donati, Daniele,D'Alessio, Roberto

, p. 437 - 450 (2013/04/10)

Valosine containing protein (VCP), also known as p97, is a member of AAA ATPase family that is involved in several biological processes and plays a central role in the ubiquitin-mediated degradation of misfolded proteins. VCP is an ubiquitously expressed, highly abundant protein and has been found overexpressed in many tumor types, sometimes associated with poor prognosis. In this respect, VCP has recently received a great deal of attention as a potential new target for cancer therapy. In this paper, the discovery and structure-activity relationships of alkylsulfanyl-1,2,4-triazoles, a new class of potent, allosteric VCP inhibitors, are described. Medicinal chemistry manipulation of compound 1, identified via HTS, led to the discovery of potent and selective inhibitors with submicromolar activity in cells and clear mechanism of action at consistent doses. This represents a first step toward a new class of potential anticancer agents.

SYNTHESIS AND BIOLOGICAL ACTIVITY OF SOME HETEROCYCLIC s-TRIAZOLE DERIVATIVES

Abdel-Raham, Abdu E.,Awad, Ibrahim M. A.,Bakhite, Etify A.

, p. 289 - 295 (2007/10/02)

3-Aryloxymethyl-4-phenyl-5-mercapto-s-triazoles (1a-c) were condensed, in the presence of a basic catalyst, with various alkyl/aralkyl halides affording different new thioethers 2a-i, 3a-c, 4a-l and 5a-c respectively.Treatment of 5a-c with hydrazine hydra

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