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Nα-acetyl-6-fluoro-D-tryptophan is a synthetic derivative of the naturally occurring amino acid tryptophan. It features a fluorine atom at the 6-position of the indole ring, which can significantly alter the chemical and biological properties of the molecule compared to the parent compound. The Nα-acetyl group provides additional protection to the amino group, which can be important in certain chemical reactions or biological assays to prevent unwanted side reactions. Nα-acetyl-6-fluoro-D-tryptophan is often used in medicinal chemistry and drug design due to its potential to modulate protein-ligand interactions and its ability to probe the binding sites of enzymes and receptors. The presence of the fluorine atom can enhance the molecule's metabolic stability and potentially its pharmacokinetic properties, making it a valuable tool in the development of new therapeutic agents.

7592-43-0

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7592-43-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7592-43-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7592-43:
(6*7)+(5*5)+(4*9)+(3*2)+(2*4)+(1*3)=120
120 % 10 = 0
So 7592-43-0 is a valid CAS Registry Number.

7592-43-0Downstream Products

7592-43-0Relevant academic research and scientific papers

Synthesis of tripeptides containing d-Trp substituted at the indole ring, assessment of opioid receptor binding and in vivo central antinociception

De Marco, Rossella,Bedini, Andrea,Spampinato, Santi,Gentilucci, Luca

supporting information, p. 6861 - 6866 (2014/10/15)

The noncationizable tripeptide Ac-d-Trp-Phe-GlyNH2 was recently proposed as a novel minimal recognition motif for μ-opioid receptor. The introduction of different substituents (methyl, halogens, nitro, etc.) at the indole of d-Trp significantly influenced receptor affinities and resulted in serum stability and in a measurable effect on central antinociception in mice after ip administration.

The facile synthesis of a series of tryptophan derivatives

Blaser, Georg,Sanderson, John M.,Batsanov, Andrei S.,Howard, Judith A.K.

, p. 2795 - 2798 (2008/09/19)

This study reports a facile method for the synthesis of a variety of 5- and 6-substituted tryptophan derivatives that are difficult to prepare using alternative enzymatic approaches. Acylation of an activated amino acid, derived from serine in situ, is coupled with an enzymatic resolution step to furnish enantiopure analogues bearing a range of electron withdrawing and releasing substituents. Isolation of a dehydroalanine derivative as a by-product from some reactions provides some insights into the likely mechanism of the reaction.

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