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tert-butyl (2-((1-(4-((6-methoxy-2-phenylpyrimidin-4-yl)oxy)-3-vinylphenyl)-2-oxo-2-((4-((pent-4-en-1-ylsulfonyl)carbamoyl)phenyl)amino)ethyl)amino)-2-oxoethyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1450789-75-9

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1450789-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1450789-75-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,0,7,8 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1450789-75:
(9*1)+(8*4)+(7*5)+(6*0)+(5*7)+(4*8)+(3*9)+(2*7)+(1*5)=189
189 % 10 = 9
So 1450789-75-9 is a valid CAS Registry Number.

1450789-75-9Relevant academic research and scientific papers

Novel peptidomimetic hepatitis C virus NS3/4A protease inhibitors spanning the P2-P1′ region

Lampa, Anna K.,Bergman, Sara M.,Gustafsson, Sofia S.,Alogheli, Hiba,Akerblom, Eva B.,Lindeberg, Gunnar G.,Svensson, Richard M.,Artursson, Per,Danielson, U. Helena,Karlen, Anders,Sandstroem, Anja

supporting information, p. 249 - 254 (2014/04/03)

Herein, novel hepatitis C virus NS3/4A protease inhibitors based on a P2 pyrimidinyloxyphenylglycine in combination with various regioisomers of an aryl acyl sulfonamide functionality in P1 are presented. The P1′ 4-(trifluoromethyl)phenyl side chain was shown to be particularly beneficial in terms of inhibitory potency. Several inhibitors with Ki-values in the nanomolar range were developed and included identification of promising P3-truncated inhibitors spanning from P2-P1′. Of several different P2 capping groups that were evaluated, a preference for the sterically congested Boc group was revealed. The inhibitors were found to retain inhibitory potencies for A156T, D168V, and R155K variants of the protease. Furthermore, in vitro pharmacokinetic profiling showed several beneficial effects on metabolic stability as well as on apparent intestinal permeability from both P3 truncation and the use of the P1′ 4-(trifluoromethyl)phenyl side chain.

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