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Structure of 49758-35-2
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L-7-Azatryptophan features a nitrogen substitution at the C7 position of the indole ring, introducing a polar, electron-deficient moiety that enhances solubility and alters binding interactions. This analog integrates seamlessly into peptide sequences under standard coupling conditions, enabling site-specific incorporation to probe protein structure-function relationships and modulate pharmacokinetic properties in bioactive peptides.
L-7-Azatryptophan serves as a bioisostere of tryptophan, enabling targeted incorporation into peptides to probe indole ring functionality in biological systems. Its pyrrole nitrogen substitution enhances metabolic stability and modulates electronic properties, facilitating studies in receptor binding and protein folding. The compound exhibits robust bench stability and compatibility with standard solid-phase peptide synthesis protocols, offering reliable access to labeled or modified biologically active sequences.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: