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N-((S)-1-(((2S,3S)-5-(((S)-1-(((S)-1-amino-4-methyl-1-oxopentan-2-yl)amino)-3-cyano-1-oxopropan-2-yl)amino)-3-hydroxy-5-oxo-1-phenylpentan-2-yl)amino)-3-methyl-1-oxobutan-2-yl)picolinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1227870-53-2

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1227870-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1227870-53-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,7,8,7 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1227870-53:
(9*1)+(8*2)+(7*2)+(6*7)+(5*8)+(4*7)+(3*0)+(2*5)+(1*3)=162
162 % 10 = 2
So 1227870-53-2 is a valid CAS Registry Number.

1227870-53-2Downstream Products

1227870-53-2Relevant academic research and scientific papers

Mechanism-based inhibitors of the aspartyl protease plasmepsin II as potential antimalarial agents

Gupta, Deepak,Yedidi, Ravikiran S.,Varghese, Sheeba,Kovari, Ladislau C.,Woster, Patrick M.

experimental part, p. 4234 - 4247 (2010/08/22)

Four aspartyl proteases known as plasmepsins are involved in the degradation of hemoglobin by Plasmodium falciparum, which causes a large percentage of malaria deaths. The enzyme plasmepsin II (Plm-II) is the most extensively studied of these aspartyl proteases and catalyzes the initial step in the breakdown of hemoglobin by the parasite. Several groups have reported the design, synthesis, and evaluation of reversible peptidomimetic inhibitors of Plm II as potential antimalarial agents. We now report four peptidomimetic analogues, compounds 6-9, which are rationally designed to act as mechanism-based inhibitors of Plm II. Three of these analogues produce potent irreversible inactivation of the enzyme with IC50 values in the low nanomolar range. Of these three compounds, two retain the low micromolar IC 50 values of the parent compound in Plasmodium falciparum (clone 3D7) infected erythrocytes. These analogues are the first examples of fully characterized mechanism-based inactivators for an aspartyl protease and show promise as novel antimalarial agents.

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