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1-(3-chlorophenyl)-4-[1-(4-cyano-3-fluorobenzyl)-5-imidazolylmethyl]-2-piperazinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

355126-33-9

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355126-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 355126-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,5,1,2 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 355126-33:
(8*3)+(7*5)+(6*5)+(5*1)+(4*2)+(3*6)+(2*3)+(1*3)=129
129 % 10 = 9
So 355126-33-9 is a valid CAS Registry Number.

355126-33-9Downstream Products

355126-33-9Relevant academic research and scientific papers

Inhibitors of prenyl-protein transferase

-

, (2008/06/13)

The present invention comprises piperazinone-containing compounds which inhibit prenyl-protein transferases, including famesyl-protein transferase and geranylgeranyl-protein transferase type I. Such therapeutic compounds are useful in the treatment of cancer.

Inhibitors of prenyl-protein transferase

-

, (2008/06/13)

The present invention comprises piperazinone-containing compounds, which may be useful as inhibitors of prenyl-protein transferases, including farnesyl-protein transferase and geranylgeranyl-protein transferase type I. Such therapeutic compounds are useful in the treatment of cancer.

Aryloxy substituted N-arylpiperazinones as dual inhibitors of farnesyltransferase and geranylgeranyltransferase-I

Bergman, Jeffrey M,Abrams, Marc T,Davide, Joseph P,Greenberg, Ian B,Robinson, Ronald G,Buser, Carolyn A,Huber, Hans E,Koblan, Kenneth S,Kohl, Nancy E,Lobell, Robert B,Graham, Samuel L,Hartman, George D,Williams, Theresa M,Dinsmore, Christopher J

, p. 1411 - 1415 (2007/10/03)

A series of aryloxy substituted piperazinones with dual farnesyltransferase/geranylgeranyltransferase-I inhibitory activity was prepared. These compounds were found to have potent inhibitory activity in vitro and are promising agents for the inhibition of

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