3303-31-9CC(C)C[C@H](NC(=O)[C@@H]([NH3+])CC(C)C)C(=O)[O-]LCPYQJIKPJDLLB-UWVGGRQHSA-NLeu-Leu zwitterion is an L-aminoacyl-L-amino acid zwitterion resulting from transfer of a proton from the carboxy to the amino group of L-leucyl-L-leucine; major species at pH 7.3. It is a tautomer of a Leu-Leu.
3303-31-9CHEBI:191208Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.
UsesLeu-Leu-OH (L-Leucyl-L-leucine), a Leu derivative, is a neutral dipeptide that can be used to study the functionality of dileucine motifs[1].
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DefinitionChEBI: A dipeptide formed from two L-leucine residues.