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(S)-2-[(R)-2-((S)-5-Amino-2-{(S)-2-[(S)-2-[(S)-3-carboxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionylamino]-3-(1H-indol-3-yl)-propionylamino]-3-methyl-butyrylamino}-pentanoylamino)-3-phenyl-propionylamino]-succinamic acid allyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

667900-55-2

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667900-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 667900-55-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,7,9,0 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 667900-55:
(8*6)+(7*6)+(6*7)+(5*9)+(4*0)+(3*0)+(2*5)+(1*5)=192
192 % 10 = 2
So 667900-55-2 is a valid CAS Registry Number.

667900-55-2Upstream product

667900-55-2Relevant academic research and scientific papers

Synthesis of Cyclic Hexapeptides Based on the Antibiotic Cyclic Decapeptide Loloatin C by an in situ Indirect Cyclization Method

Chen, Heru,Haynes, Richard K.,Scherkenbeck, Juergen

, p. 38 - 47 (2004)

Three cyclic hexapeptide units based on the parent loloatin C scaffold have been identified by a 'sliding window' method as part of an expeditious SAR search for the basis of the antibiotic activity of the lolatins.Modified Fmoc-based solid-phase synthesis was used to prepare cyclic(L-valyl-l-ornithyl-D-phenylalanyl-l-asparaginyl-L-aspartyl-L-tryptophanyl) and cylic(L-valyl-L-ornithyl-l-leucyl-l-tryptophanyl-D-phenylalanyl-L-asparaginyl) in overall yields of 42 percent-47 percent. A new solution method combined with an in situ indirect cyclization was specifically developed to prepare cyclic(L-ornithyl-L-leucyl-D-tyrosyl-L-prolyl-L-tryptophanyl-D-phenylalanyl), involving cyclization of the linear peptide through the amino group in leucine, liberated selectively from the Fmoc-protected amine in situ, with the activated p-nitrophenyl ester of ornithine. The method was also effectively used for cyclization of the linear precursors of the first two cyclic hexapeptides. NOE analyses coupled with peptide backbone modelling were used to establish conformations of the target compounds. All have helix-like structures with γ-turns.

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