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2-(4-chloro-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-1-(4-iodophenyl)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1443752-69-9

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1443752-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1443752-69-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,3,7,5 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1443752-69:
(9*1)+(8*4)+(7*4)+(6*3)+(5*7)+(4*5)+(3*2)+(2*6)+(1*9)=169
169 % 10 = 9
So 1443752-69-9 is a valid CAS Registry Number.

1443752-69-9Relevant academic research and scientific papers

Design, synthesis, and biological evaluation of pyrazolo[3,4-d]pyrimidines active in vivo on the Bcr-Abl T315I mutant

Radi, Marco,Tintori, Cristina,Musumeci, Francesca,Brullo, Chiara,Zamperini, Claudio,Dreassi, Elena,Fallacara, Anna Lucia,Vignaroli, Giulia,Crespan, Emmanuele,Zanoli, Samantha,Laurenzana, Ilaria,Filippi, Irene,Maga, Giovanni,Schenone, Silvia,Angelucci, Adriano,Botta, Maurizio

, p. 5382 - 5394 (2013/07/26)

Starting from our in-house library of pyrazolo[3,4-d]pyrimidines, a cross-docking simulation was conducted on Bcr-Abl T315I mutant. Among the selected compounds (2a-e), the 4-bromo derivative 2b showed the best activity against the Bcr-Abl T315I mutant. Deeper computational studies highlighted the importance of the bromine atom in the para position of the N1 side chain phenyl ring for the interaction with the T315I mutant. A series of 4-bromo derivatives was thus synthesized and biologically evaluated. Compound 2j showed a good balance of different ADME properties, high activity in cell-free assays, and a submicromolar potency against T315I Bcr-Abl expressing cells. In addition, it was converted into a water-soluble formulation by liposome encapsulation, preserving a good activity on leukemic T315I cells and avoiding the use of DMSO as solubilizing agent. In vivo studies on mice inoculated with 32D-T315I cells and treated with 2j showed a more than 50% reduction in tumor volumes.

An alternative synthetic approach for the synthesis of biologically relevant 1,4-disubstituted pyrazolo[3,4-d]pyrimidines

Radi, Marco,Bernardo, Vincenzo,Vignaroli, Giulia,Brai, Annalaura,Biava, Mariangela,Schenone, Silvia,Botta, Maurizio

supporting information, p. 5204 - 5206 (2013/09/02)

A versatile approach for the synthesis of 1,4-disubstituted pyrazolo[3,4-d]pyrimidines has been developed. Starting from commercially available allopurinol, TBAF mediated N1-functionalization and subsequent C4 nucleophilic substitution, under microwave assisted- or standard heating conditions, granted access to highly functionalized pyrazolo[3,4-d]pyrimidines of potential biological interest.

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