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4-(2-aminoethyl)-2,6-difluorophenol hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59043-65-1

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59043-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59043-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,4 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59043-65:
(7*5)+(6*9)+(5*0)+(4*4)+(3*3)+(2*6)+(1*5)=131
131 % 10 = 1
So 59043-65-1 is a valid CAS Registry Number.

59043-65-1Downstream Products

59043-65-1Relevant academic research and scientific papers

ASPARAGINE DERIVATIVES AND METHODS OF USE THEREOF

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Paragraph 00801; 00803-00804, (2021/12/31)

The present invention relates to compounds of formulas (A) and (I), pharmaceutically acceptable salts thereof, and solvates of any of them, pharmaceutical compositions comprising them, methods of preparation thereof, intermediate compounds useful for the preparation thereof, and methods of treatment or prophylaxis of diseases, in particular cancer, such as colorectal cancer, using these. (A) (I)

Design, synthesis and biological evaluation of ezrin inhibitors targeting metastatic osteosarcoma

Paige, Mikell,Kosturko, George,Bulut, Güllay,Miessau, Matthew,Rahim, Said,Toretsky, Jeffrey A.,Brown, Milton L.,üren, Aykut

, p. 478 - 487 (2014/01/17)

Respiratory failure due to pulmonary metastasis is the major cause of death for patients with osteosarcoma. However, the molecular basis for metastasis of osteosarcoma is poorly understood. Recently, ezrin, a member of the ERM family of proteins, has been associated with osteosarcoma metastasis to the lungs. The small molecule NSC 668394 was identified to bind to ezrin, inhibit in vitro and in vivo cell migration, invasion, and metastatic colony survival. Reported herein are the design and synthesis of analogues of NSC 668394, and subsequent functional ezrin inhibition studies. The binding affinity was characterized by surface plasmon resonance technique. Cell migration and invasion activity was determined by electrical cell impedance methodology. Optimization of a series of heterocyclic-dione analogues led to the discovery of compounds 21k and 21m as potential novel antimetastatic agents.

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