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(2S,4S,5S)-5-amino-6-cyclohexyl-4-hydroxy-2-isopropyl hexanoic acid n-butyl amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105852-64-0

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105852-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105852-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,5 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 105852-64:
(8*1)+(7*0)+(6*5)+(5*8)+(4*5)+(3*2)+(2*6)+(1*4)=120
120 % 10 = 0
So 105852-64-0 is a valid CAS Registry Number.

105852-64-0Downstream Products

105852-64-0Relevant academic research and scientific papers

Synthesis of the hydroxyethylene dipeptide isostere, (2S,4S,5S)-5-amino-6-cyclohexyl-4-hydroxy-2-isopropyl hexanoic acid n-butyl amide

Poss,Reid

, p. 1411 - 1414 (2007/10/02)

A stereoselective synthesis of the hydroxyethylene dipeptide isostere, (2S,4S,5S)-5-amino-6-cyclohexyl-4-hydroxy-2-isopropyl hexanoic acid-n-butyl amide from Boc-L-phenylalanine is described.

5-(HETEROCYCLYLALKANOYL)AMINO-4-HYDROXYPENTANAMIDES

-

, (2008/06/13)

This invention concerns novel nitrogen derivatives of the formula I STR1 (and their pharmaceutically-acceptable salts), together with pharmaceutical compositions containing them. The nitrogen derivatives are inhibitors of the catalytic action of renin. Th

1,2,4-Triazolopyrazine Derivatives with Human Renin Inhibitory Activity. 2. Synthesis, Biological Properties and Molecular Modeling of Hydroxyethylene Isostere Derivatives

Bradbury, Robert H.,Major, John S.,Oldham, Alec A.,Rivett, Janet E.,Roberts, David A.,et al.

, p. 2335 - 2342 (2007/10/02)

A series of inhibitors of human renin have been synthesized, derived from combination of a 2-(8-propyl-6-pyridin-3-yl-1,2,4-triazolopyrazin-3-yl)-3-pyridin-3-ylpropionic acid moiety 6c with the hydroxyethylene isostere of the scissile amide bond (2

A Versatile and Stereocontrolled Synthesis of Hydroxyethylene Dipeptide Isosteres

Herold, Peter,Duthaler, Rudolph,Rihs, Grety,Angst, Christof

, p. 1178 - 1185 (2007/10/02)

An asymmetric synthesis of the hydroxyethylene dipeptide isostere unit 1 is described.The synthesis provides excellent stereocontrol over all three chiral centers and is amenable to variation of substituents R1 and R2.Key intermediat

THE SYNTHESIS OF (2S,4S,5S)-5-(N-BOC)-AMINO-6-CYCLOHEXYL-4-HYDORXY-2-ISOPROPYL-HEXANOIC ACID LACTONE, AN HYDROXYETHYLENE DIPEPTIDE ISOSTERE PRECURSOR

Chakravarty, Prasun K.,Laszlo, Stephen E. de,Sarnella, Carol S.,Springer, James P.,Schuda, Paul F.

, p. 415 - 418 (2007/10/02)

(2SR,4SR)-5-(S)-(N-Boc)-amino-cyclohexyl-4-hydroxy-2-isopropyl hexanoivc acid from (L)-phenylalanine and the preparation of the n-butyl amide of the 2(S),4(S),5(S) acid is presented.

Synthesis and biological activity of some transition-state inhibitors of human renin

Buhlmayer,Caselli,Fuhrer,Goschke,Rasetti,Rueger,Stanton,Criscione,Wood

, p. 1839 - 1846 (2007/10/02)

A series of renin inhibitors containing the dipeptide transition state mimics (2S,4S,5S)-5-amino-4-hydroxy-2-isopropyl-7-methyloctanoic acid (Leu-(OH)-Val) and (2S,4S,5S)-5-amino-4-hydroxy-2-isopropyl-6-cyclohexylhexanoic acid (Cha-(OH)-Val) was prepared.

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