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78731-97-2

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  • L-Cysteine,S-[(acetylamino)methyl]-N-[N-[N-[N-[N-[N2-[N-[N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl]-L-tryptophyl]-N6-[[2-(methylsulfonyl)ethoxy]carbonyl]-L-lysyl]-L-threonyl]-L-phenylalanyl]-L-t

    Cas No: 78731-97-2

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78731-97-2 Usage

General Description

L-Cysteine, S-[(acetylamino)methyl]-N-[N-[N-[N-[N-[N2-[N-[N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl]-L-tryptophyl]-N6-[[2-(methylsulfonyl)ethoxy]carbonyl]-L-lysyl]-L-threonyl]-L-phenylalanyl]-L-threonyl]-L-seryl]-,2-[[[4-(phenylazo)phenyl]methyl]sulfonyl]ethyl ester (9CI) is a complex chemical compound that includes L-Cysteine as well as other amino acids like alanine, phenylalanine, tryptophan, lysine, threonine, and serine. It also contains acetyl and methyl groups, as well as a sulfonyl-phenylazo-phenylmethyl group. L-Cysteine,S-[(acetylamino)methyl]-N-[N-[N-[N-[N-[N2-[N-[N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl]-L-tryptophyl]-N6-[[2-(methylsulfonyl)ethoxy]carbonyl]-L-lysyl]-L-threonyl]-L-phenylalanyl]-L-threonyl]-L-seryl]-,2-[[[4-(phenylazo)phenyl]methyl]sulfonyl]ethyl ester (9CI) has a long and intricate structure with multiple functional groups and side chains, suggesting potential biological or pharmacological activity or interactions.

Check Digit Verification of cas no

The CAS Registry Mumber 78731-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,3 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78731-97:
(7*7)+(6*8)+(5*7)+(4*3)+(3*1)+(2*9)+(1*7)=172
172 % 10 = 2
So 78731-97-2 is a valid CAS Registry Number.

78731-97-2Relevant articles and documents

New analogs of somatostatin with unexpected effects in vivo on insulin basal secretion in the rat

Diaz,Cazaubon,Demarne,et al.

, p. 219 - 227 (2007/10/02)

Twenty analogs of somatostatin were synthesized by the alternating solution/solid-phase procedure. The peptide analogs contained taurine, aza-alanine, or D-amino acids as well as multiple deletions. The aim of this study was to obtain analogs that would selectively inhibit insulin or glucagon release. The biological activities were evaluated in vivo in the rat by measuring the effects of the modified somatostatin molecules on basal secretion of insulin and glucagon in the portal vein. Although some selective analogs were found, a few of them having a taurine or an aza-alanine residue in their structure caused a significant increase of insulin secretion. This unexpected phenomenon, for which we do not have an explanation at present, is under investigation.

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