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Structure of 2407830-01-5
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(S)-N-Fmoc-N-Methyl-3-cyclopentyl-Ala features a chiral cyclopentyl side chain that enhances conformational rigidity in peptide synthesis. The Fmoc group enables efficient, base-labile N-terminal protection, while the N-methyl substitution reduces amide hydrogen bonding, improving membrane permeability and metabolic stability in bioactive sequences.
(S)-N-Fmoc-N-Methyl-3-cyclopentyl-Ala serves as a versatile, bench-stable building block for the synthesis of peptidomimetics and bioactive oligomers. Its Fmoc protection enables efficient solid-phase peptide synthesis, while the N-methyl group enhances metabolic stability and membrane permeability. The 3-cyclopentyl side chain provides conformational rigidity and hydrophobic character, facilitating targeted interactions in medicinal chemistry applications.
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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: